(Q34709047)

4 August 2017

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title

Pericentric inversions. Problems and significance for clinical genetics (English)

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4 August 2017

Kaiser P

1

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4 August 2017

1 January 1984

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4 August 2017

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4 August 2017

68

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4 August 2017

1-47

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4 August 2017

1

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https://scigraph.springernature.com/pub.10.1007/bf00293869

4 August 2017

0 references

cites work

Trisomy for the distal segment of chromosome 13: a new syndrome

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF00293869

X-ray induced pericentric inversions in Anopheles albimanus

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF00293869

Glossary of Genetics and Cytogenetics – Classical and Molecular

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF00293869

Meiotic analysis of a pericentric inversion, inv(7) (p22q32), in the father of a child with a duplication-deletion of chromosome 7

21 January 2018

1 reference

12 December 2020

Inherited pericentric inversion of a human Y chromosome in trisomic Down's syndrome

1 reference

12 December 2020

Peri- and paracentric inversions in chromosome 12: prenatal diagnosis and family study

1 reference

12 December 2020

The effect of structural aberrations of the chromosomes on reproductive fitness in man. II. Results

1 reference

12 December 2020

1 reference

12 December 2020

Chromosome anomalies among livebirths

1 reference

12 December 2020

Apparently balanced de novo translocations in patients with abnormal phenotypes: report of 6 cases

1 reference

12 December 2020

Chromosome studies in a neonatal population.

1 reference

12 December 2020

Inversion of 'flourescent' segment in chromosome 3: a polymorphic trait.

1 reference

12 December 2020

[Chromosomal phylogeny of man and the anthropomorphic primates. (Pan troglodytes, Gorilla gorilla, Pongo pygmaeus). Attempt at reconstitution of the karyotype of the common ancestor].

1 reference

12 December 2020

Chromosomal Localization of Mouse Satellite DNA

1 reference

12 December 2020

[Trisomy 21 and abnormality of structure of the Y]

1 reference

12 December 2020

Assignment of the major histocompatibility complex to chromosome No. 6 in a family with a pericentric inversion.

1 reference

12 December 2020

Partial trisomy 13q21?qter de novo due to a recombinant chromosome rec(13)dup q

1 reference

12 December 2020

Complex de novo rearrangement of chromosome 9 with clinical features of monosomy 9p syndrome

1 reference

12 December 2020

Somatic pairing and meiotic nonrandom disjunction in a pericentric inversion of Hylemya antiqua (Meigen).

1 reference

12 December 2020

Familial inversion of chromosome No. 8: an affected child and a carrier fetus

1 reference

12 December 2020

The effect of structural aberrations of the chromosomes on reproductive fitness in man

1 reference

12 December 2020

On the number of ribosomal RNA genes in man

1 reference

12 December 2020

DIFFERENCE IN THE BEHAVIOR OF EU- AND HETERO-CHROMATIN: CROSSING-OVER.

1 reference

12 December 2020

A clinical and cytogenetic investigation carried out in a special institution for mentally retarded patients: preliminary results concerning 82 cases of oligophrenia (author's transl)

1 reference

12 December 2020

Mosaic-trisomy and pericentric inversion of chromosome 9 in a malformed boy.

1 reference

12 December 2020

Pericentric inversion of a chromosome 21. Study of 3 generations. Genetic counseling

1 reference

12 December 2020

Position effect variegation in the mouse

1 reference

12 December 2020

Pericentric inversion (13) with two different recombinants in the same family.

1 reference

12 December 2020

Pericentric X chromosome in a family

1 reference

12 December 2020

Inherited pericentric inversion of chromosome 5: a family with history of neonatal death and a case of the "cri du chat" syndrome

1 reference

12 December 2020

Duplication/deficiency product of a pericentric inversion in man: A cause of D1 trisomy syndrome

1 reference

12 December 2020

Value in prenatal diagnosis of new technics for chromosome identification in translocations and a recombination aneusomia

1 reference

12 December 2020

A further chromosome analysis in induced abortions (author's transl)

1 reference

12 December 2020

Karyotype with chromosomal abnormality with various inherited defects in the offspring (Recombination aneusomy)

1 reference

12 December 2020

Pericentric inversion of chromosome 4 : inv (4) (p13, q35) and trisomy of the short branch of chromosome 4 due to recombination aneusomy

1 reference

12 December 2020

A pericentric inversion of chromosome 9 and a rearrangement involving chromosomes 9 and 10, observed in two generations. Clinical description of chromosome 9 (p12-p21) deletion syndrome

1 reference

12 December 2020

Trisomy 9p resulting from de novo 9/15 translocation and a 9p isochromosome

1 reference

12 December 2020

Trisomy 9 mosaicism in a newborn infant with multiple malformations.

1 reference

12 December 2020

CHROMOSOME STUDIES IN FIVE CASES OF COLOBOMA OF THE IRIS

1 reference

12 December 2020

Aneusomie de recombinaison: three further examples

1 reference

12 December 2020

Duplication-deletion syndrome in a family with pericentric inversion of chromosome 6

1 reference

12 December 2020

Elucidation of a pericentric inversion of a D-group chromosome in the mother of a child with Patau's syndrome

1 reference

12 December 2020

Pericentric inversion of chromosome No. 8

1 reference

12 December 2020

Pericentric enversion of chromosome no. 13 in a large family leading to duplication deficiency causing congenital malformations in three individuals

1 reference

12 December 2020

[Comparison of the structure of chromatids of Homo sapiens and Pan troglodytes (author's transl)]

1 reference

12 December 2020

Familial pericentric inversion of chromosome 2

1 reference

12 December 2020

Minor chromosome variations and selected heteromorphisms in 200 unclassifiable mentally retarded patients and 200 normal controls

1 reference

12 December 2020

C- and Q-band polymorphisms in the chromosomes of three human populations

1 reference

12 December 2020

Study on segregation of the inversion of chromosome 4 (p15.2q11) in two unrelated families

1 reference

12 December 2020

HL-A Antigens and Heteromorphic Fluorescence Characters of Chromosomes in Prenatal Paternity Investigation

1 reference

12 December 2020

Chromosomal heteromorphisms in the assignment of loci to particular autosomes: a study of four pedigrees

1 reference

12 December 2020

Marker chromosomes in parents of spontaneous abortuses

1 reference

12 December 2020

Cytological demonstration of mitotic crossing-over in man

1 reference

12 December 2020

Localization of heterochromatin in human chromosomes.

1 reference

12 December 2020

1q plus variants in a normal adult population (one with a pericentric inversion)

1 reference

12 December 2020

Banding patterns of the chromosomes of man and gorilla

1 reference

12 December 2020

Pericentric inversions and reproductive loss

1 reference

12 December 2020

Chromosome analysis on 930 consecutive newborn children using quinacrine fluorescent banding technique

1 reference

12 December 2020

Familial incidence of pericentric inversion of X chromosome

1 reference

12 December 2020

Partial Deletion of 1q, Following a Pericentric Inversion, in a Boy with Multiple Minor Morphologic Anomalies and Mental Retardation

1 reference

12 December 2020

Partial and complete trisomy 9: Delineation of a trisomy 9 syndrome

1 reference

12 December 2020

Incidence of major chromosome abnormalities in children

1 reference

12 December 2020

A new pericentric inversion of chromosome 6 in an abnormal infant

1 reference

12 December 2020

Pericentric inversions of human chromosomes 9 and 10.

1 reference

12 December 2020

The accurate estimation of chromatid breakage, and its relevance to a new interpretation of chromatid aberrations induced by ionizing radiations

1 reference

12 December 2020

Chromosome studies in investigation of stillbirths and neonatal deaths

1 reference

12 December 2020

Three families with pericentric inversion of chromosome 9

1 reference

12 December 2020

Chromosomal evolution in Primates: Tentative phylogeny from Microcebus murinus (Prosimian) to man

1 reference

12 December 2020

The meiotic consequences of chromosome modifications

1 reference

12 December 2020

1 reference

12 December 2020

Balanced and unbalanced pericentric inversion of chromosome 11

1 reference

12 December 2020

A retarded child with a 46XX,3p-q+ chromosome karyotype

1 reference

12 December 2020

Familial pericentric inversion of chromosome 19, inv(19) (p13q13) with a note on genetic counseling of pericentric inversion carriers

1 reference

12 December 2020

1 reference

12 December 2020

Structural variation in chromosome No 9.

1 reference

12 December 2020

[Staining of human chromosomes with acridine orange after treatment with 5 bromodeoxyuridine]

1 reference

12 December 2020

[Total percentric inversion of chromosome 9 as positive proof of in the legal determination of paternity]

1 reference

12 December 2020

Pericentric inversion and partial monosomy 4q associated with congenital anomalies

1 reference

12 December 2020

Pericentric inversion of chromosome 21. A possible further cytogenetic mechanism in mongolism

1 reference

12 December 2020

Inversion duplication of chromosome 6 with trisomic codominant expression of HLA antigens

1 reference

12 December 2020

Identification of translocation chromosomes by quinacrine fluorescence.

1 reference

12 December 2020

Chromosome studies in 500 induced abortions

1 reference

12 December 2020

Chromosome studies in full-term, low-birth-weight, mentally retarded patients.

1 reference

12 December 2020

Duplication of a segment of chromosome 3 in a subject with multiple congenital anomalies and a 47,XYY father, inversion of chromosomes 3 and 9 in the mother, and inversion of chromosome 9 in a brother

1 reference

12 December 2020

Trisomy 10p produced by recombination involving maternal inversion inv(10)(pllq26).

1 reference

12 December 2020

Trisomy 22q12 leads to qter: "aneusomie de recombinaison" of a pericentric inversion

1 reference

12 December 2020

Chromosome 7 in ataxia-telangiectasia

1 reference

12 December 2020

Karyotypic evolution in man and chimpanzees. A comparative study of band topographies after controlled denaturation

1 reference

12 December 2020

Polymorphism of Human Constitutive Heterochromatin

1 reference

12 December 2020

Familial pericentric inversion of chromosome 8 : is breakpoint p22q23 important in the formation of unbalanced recombinants?

1 reference

12 December 2020

Cytological assessment of meiotic exchange in a human male with a pericentric inversion of chromosome No. 4

1 reference

12 December 2020

Phenotypically normal individuals with an inversion (X) (p22q13) and the recombinant (X), dup q

1 reference

12 December 2020

Inherited pericentric inversion of chromosome number two: a linkage study

1 reference

12 December 2020

Satellite DNA and cytological staining patterns in heterochromatic inversions of human chromosome 9

1 reference

12 December 2020

Analysis of the karyotype of Pan paniscus. Comparison with other Pongidae and man (author's transl)

1 reference

12 December 2020

Chromosome findings in 700 children referred to a psychiatric clinic

1 reference

12 December 2020

The gorilla karyotype: chromosome lengths and polymorphisms

1 reference

12 December 2020

Precise identification of various chromosomal abnormalities.

1 reference

12 December 2020

Chromosome polymorphism in a human newborn population. II. Potentials of polymorphic chromosome variants for characterizing the idiogram of an individual

1 reference

12 December 2020

Abnormal X chromosomes in man: Origin, behavior and effects

1 reference

12 December 2020

Cytological mapping of human chromosomes: results obtained with quinacrine fluorescence and the acetic-saline-Giemsa techniques

1 reference

12 December 2020

A cytogenetic study of recurrent abortion

1 reference

12 December 2020

Duplication-deficiency of chromosome 18, resulting from recombination of a paternal pericentric invesion, with a note for genetic counselling

1 reference

12 December 2020

Observations on the satellited human chromosomes

1 reference

12 December 2020

An XYY boy with short stature and a case of Klinefelter's syndrome (XXY) in a family with inversion 9

1 reference

12 December 2020

Turner's syndrome with a duplication-deficiency X chromosome derived from a maternal pericentric inversion X chromosome

1 reference

12 December 2020

Cytogenetic analysis of major heterochromatic elements (especially Xh and Y) in Drosophila melanogaster, and the theory of "heterochromatin".

1 reference

12 December 2020

Clinical and chromosomal studies of the 18q-syndrome

1 reference

12 December 2020

Polymporphism of human C-band heterochromatin. II. Family studies with suggestive evidence for somatic crossing over

1 reference

12 December 2020

Pericentric inversion, inv(9) (p22 q32), in the father of a child with a duplication-deletion of chromosome 9 and gene dosage effect for adenylate kinase-1

1 reference

12 December 2020

A case of chromosome 3 duplication q deletion p syndrome born to the mother with a pericentric inversion, inv(3)(p25q21)

1 reference

12 December 2020

Pericentric inversion in a group D chromosome (13?15) associated with amenorrhea and gonadal dysgenesis

1 reference

12 December 2020

Pericentric inversions. Report on two malformation cases suggestive of parental inversion heterozygosity

1 reference

12 December 2020

Chromosomal anomalies with special reference to Klinefelter's syndrome

1 reference

12 December 2020

The sites and relative frequencies of secondary constrictions in human somatic chromosomes

1 reference

12 December 2020

An analysis of the break points of structural rearrangements in man

1 reference

12 December 2020

Inversion 19 and isochromosome short arm 17 or 18

1 reference

12 December 2020

Segregation of ABO, AK1and ACONSin families with abnormalities of chromosome 9

1 reference

12 December 2020

The value of fluorescence markers in the distinction between maternal and fetal chromosomes

1 reference

12 December 2020

Inversion homozygosity of chromosome no. 9 in a higly inbred kindred

1 reference

12 December 2020

Chromosome variation and gene action

1 reference

12 December 2020

Frequency of 9qh+ and risk of chromosome aberrations in the progeny of individuals with 9qh+

1 reference

12 December 2020

Pericentric inversion of "fluorescent" segment in chromosome no. 3

1 reference

12 December 2020

Familial pericentric inversion of chromosome 8.

1 reference

12 December 2020

Familial pericentric inversion of chromosome 1 with a note on reproductive risks

1 reference

12 December 2020

Oligohydramnios syndrome and XYY karyotype

1 reference

12 December 2020

Pericentric inversions: studies in 47 cases

1 reference

12 December 2020

Short arm deletion of an X chromosome, 46,XXp-

1 reference

12 December 2020

Cytogenetic study of a large black kindred: inversions, heteromorphisms, and segregation analysis

1 reference

12 December 2020

1 reference

12 December 2020

Frequency of chromosome abnormalities in abortions

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12 December 2020

Distribution of sister chromatid exchanges in the euchromatin and heterochromatin of the Indian muntjac

1 reference

12 December 2020

Normal psychomotor development in a child with mosaic trisomy and pericentric inversion of chromosome 9.

1 reference

12 December 2020

Hot spots and functional organization of human chromosomes

1 reference

12 December 2020

Familial pericentric inversion of y chromosome and Down's syndrome

1 reference

12 December 2020

Banding patterns of the chromosomes of man and the chimpanzee.

1 reference

12 December 2020

Pericentric Inversions of Chromosome Number 9: Benign or Harmful?

1 reference

12 December 2020

A subtelocentric chromosome 9 in a dysplastic 18-year-old boy with dissociated mental development

1 reference

12 December 2020

Specific cytological recognition of the heterochromatic segment of number 9 chromosome in man

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12 December 2020

Structural variability of the normal human karyotype

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12 December 2020

1 reference

12 December 2020

Linkage relationships of HLA and a familial chromosome 6 inversion (pter leads to p23::q23 leads to qter): lack of dose effect in duplication-deficient offspring

1 reference

12 December 2020

Turner's syndrome and a probable pericentric inversion of chromosome 2(45, X, 2(p+q-))

1 reference

12 December 2020

Cytogenetic study of a case of Fanconi's syndrome with a familial pericentric inversion

1 reference

12 December 2020

A large pericentric inversion of human chromosome 8

1 reference

12 December 2020

The chromosomal location of human satellite DNA III

1 reference

12 December 2020

The segregation of human chromosome polymorphisms

1 reference

12 December 2020

A pericentric inversion, 5p–q+, and additional complex rearrangements in a case of cri-du-chat syndrome

1 reference

12 December 2020

Chromosome Polymorphism in American Negro and White Populations

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12 December 2020

Duplication deficiency as the result of meiotic segregation of a maternal InV (10)

1 reference

12 December 2020

[Karyotype-phenotype correlation in a 46,Xdel(X) (p22) diagnosis (author's transl)].

1 reference

12 December 2020

Prenatal detection of pericentric inversion of chromosome 12

1 reference

12 December 2020

Dicentric X-isochromosome (Xqi dic) and pericentric inversion of No. 2 inv(2) (p15) q21) in a patient with gonadal dysgenesis

1 reference

12 December 2020

Two pericentric inversions of human chromosome 11

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12 December 2020

Association of pericentric inversion of chromosome 9 and reproductive failure in ten unrelated families

1 reference

12 December 2020

A pericentric inversion of a chromosome 4 with a t(4q+10p-) and a familial t(DqDq) in a mentally retarded girl

1 reference

12 December 2020

Abnormal chromosome 22 and recurrence of trisomy-22 syndrome

1 reference

12 December 2020

The nature and inheritance of an elongated secondary constriction on chromosome 9 of man

1 reference

12 December 2020

Abnormalities resulting from a familial pericentric inversion of chromosome 18

1 reference

12 December 2020

Rieger's syndrome with pericentric inversion of chromosome 6.

1 reference

12 December 2020

Trisomy 18 in sibs and maternal chromosome 9 variant

1 reference

12 December 2020

Inherited parital duplication deficiency of chromosome 15 (p12;q22)

1 reference

12 December 2020

Pericentric inversion of chromosome 2 (p11 q13) in unrelated families (author's transl)

1 reference

12 December 2020

Abnormal childhood phenotypes associated with the same balanced chromosome rearrangements as in the parents

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12 December 2020

Pericentric inversions of chromosome 12 in two families

1 reference

12 December 2020

Structural differences in pericentric inversions. Application to a model of risk of recombinants

1 reference

12 December 2020

Study on segregation and risk for abnormal offspring in carriers of pericentric inversion of the (p11 leads to q13) segment of chromosome 2

1 reference

12 December 2020

Origin of extra chromosome in trisomy 21

1 reference

12 December 2020

Pericentric inversion of chromosome 1 in three sterile brothers

1 reference

12 December 2020

Partial monosomy and partial trisomy 18 in two offspring of carrier of pericentric inversion of chromosome 18

1 reference

12 December 2020

LBA technique in the detection of chromosome variants. II. Chromosomes except for those with Q variants

1 reference

12 December 2020

Pericentric inversion, inv(10), in a mother and aneusomy by recombination, inv(10),rec(10), in her son

1 reference

12 December 2020

Morphologic variability of human chromosomes: Polymorphism of constitutive heterochromatin

1 reference

12 December 2020

Pericentric inversion in a family with a 21/22 translocation

1 reference

12 December 2020

Chromosome studies on testicular cells from 50 subfertile men.

1 reference

12 December 2020

Human Q and C chromosomal variations: distribution and incidence

1 reference

12 December 2020

Trisomy 4p due to recombination aneusomy of an inversion 4 (p 14, q 35)

1 reference

12 December 2020

Pericentric inversion Y in a population of newborn boys.

1 reference

12 December 2020

Position of the Duffy locus on chromosome 1 in relation to breakpoints for structural rearrangements

1 reference

12 December 2020

F fing chromosome (46, XY, Fr) in a boy with multiple abnormalities

1 reference

12 December 2020

Pericentric Y-inversion.

1 reference

12 December 2020

Pericentric X chromosome ascertained during antenatal diagnosis

1 reference

12 December 2020

Familial inversions and other concomitant chromosome aberrations

1 reference

12 December 2020

New chromosome polymorphism: inv(16)(p11q12 or 13)

1 reference

12 December 2020

A balanced translocation (17;22) and a pericentric inversion of chromosome 5. Repository identification No. GM3196.

1 reference

12 December 2020

Assignment and map-positioning of human loci using chromosomal variation

1 reference

12 December 2020

The Relations of Inversions in the X Chromosome of Drosophila Melanogaster to Crossing over and Disjunction

1 reference

12 December 2020

Partial inversion of the secondary constriction of chromosome 9. Does it exist?

1 reference

12 December 2020

A probable pericentric inversion of a G-G translocation chromosome in a mentally retarded child with mongoloid traits

1 reference

12 December 2020

Pericentric inversion of chromosome 1: frequency and possible association with cancer

1 reference

12 December 2020

Deletion 14q and pericentric inversion 14

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12 December 2020

Nonrandom distribution of exchange points in patients with structural rearrangements

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12 December 2020

Application of new technics of chromosome identification to cytogenetic problems.

1 reference

12 December 2020

Autosomal polymorphisms

1 reference

12 December 2020

High frequencies of inversions and translocations of chromosomes 7 and 14 in ataxia telangiectasia

1 reference

12 December 2020

Quinacrine fluorescence and Giemsa banding in trisomy 22

1 reference

12 December 2020

A cytogenetic study of human spontaneous abortions using banding techniques

1 reference

12 December 2020

Recombinant chromosome as a result of pericentric inversion of X chromosome

1 reference

12 December 2020

Paternal pericentric inversion of chromosome 9 with a 9p+ offspring

1 reference

12 December 2020

Pericentric inversion of a number 15 chromosome in nine members of one family.

1 reference

12 December 2020

Prenatal diagnosis of trisomy 9

1 reference

12 December 2020

Banding analysis of abnormal karyotypes in spontaneous abortion

1 reference

12 December 2020

A new type of inversion of a human Y chromosome

1 reference

12 December 2020

A satellited Yq chromosome associated with trisomy 21 and an inversion of chromosome 9

1 reference

12 December 2020

Banding in human chromosomes treated with trypsin

1 reference

12 December 2020

A 17-year-old patient with dilated cardiomyopathy. Familial, pericentric inversion of chromosome 5

1 reference

12 December 2020

Structural variability of human chromosome 9 in relation to its evolution.

1 reference

12 December 2020

Cytogenetics of recurrent abortion or unsuccessful pregnancy

1 reference

12 December 2020

Location of Ribosomal DNA in the Human Chromosome Complement

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12 December 2020

Letter: A1 and C9 marker chromosomes in children with combined minor and major malformations

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12 December 2020

Balanced and unbalanced pericentric inversion of a chromosome 14

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12 December 2020

Pericentric Y inversion in the general population

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12 December 2020

Pericentric inversion of chromosome 9.

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12 December 2020

Mental retardation associated with "balanced" chromosome rearrangements

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12 December 2020

Segregation of ACP1and MNSs in families with structural rearrangements involving chromosome 2

1 reference

12 December 2020

[A case of XX-XY chimerism with normal male phenotype (author's transl)]

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12 December 2020

Length variation in the quinacrine-binding segment of human Y chromosomes of different sizes

1 reference

12 December 2020

Pericentric inversions inv(2)(p11q13) and inv(2)(p13q11) in 2 unrelated families

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12 December 2020

Are 1q plus chromosomes harmless?

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12 December 2020

Pericentric inversion in chromosome No.2 as a de novo mutation

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12 December 2020

46,Xinv(Yp+q-) in four generations of an Indian family

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12 December 2020

A simple technique for demonstrating centromeric heterochromatin

1 reference

12 December 2020

Chromosome studies in 5,049 consecutive newborn children

1 reference

12 December 2020

Trisomy 9 associated with an enlarged 9qh segment in a liveborn

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12 December 2020

Pierre Robin Syndrome in Siblings

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12 December 2020

Three cases of familial pericentric inversion 2

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12 December 2020

Population cytogenetic investigation of newborns in Moscow.

1 reference

12 December 2020

A cytogenetic survey of 14,069 newborn infants. I. Incidence of chromosome abnormalities

1 reference

12 December 2020

Fluorescent chromosome polymorphisms: frequencies and segregations in a Dutch population.

1 reference

12 December 2020

Polymorphism of human C-band heterochromatin. I. Frequency of variants

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12 December 2020

Pericentric inversion of chromosome 14 and the risk of partial duplication of 14q (14q31 → 14qter)

1 reference

12 December 2020

Differential rates of sister chromatid exchanges between euchromatin and heterochromatin

1 reference

12 December 2020

Retrospective and prospective epidemiological studies of 1500 karyotyped spontaneous human abortions

1 reference

12 December 2020

Primary Amenorrhea in a Black Female with Duplication and Inversion of the Secondary Constriction Regions of Chromosome 9*

1 reference

12 December 2020

Chromosomal aspects of human male sterility.

1 reference

12 December 2020

Partial trisomy 13 presumably due to recombination in an inversion heterozygote and by unequal crossing-over

1 reference

12 December 2020

Incidence of chromosome aberrations among 11 148 newborn children

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12 December 2020

Meiotic consequences of pericentric inversions of chromosome 13

1 reference

12 December 2020

Risk for recombinants in pericentric inversions of the (p11 leads to q21) region of chromosome 18

1 reference

12 December 2020

Chiasma distribution at diakinesis in the normal human male

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12 December 2020

Mosaic trisomy 9: two additional cases.

1 reference

12 December 2020

Maternal and paternal origin of extra chromosome in trisomy 21

1 reference

12 December 2020

A closer look at chromosomal inversions

1 reference

12 December 2020

Microdensitometric identification of the pericentric inversion of chromosome No.2 and of duplication of the short arm of chromosome No.7 in a reexamined case

1 reference

12 December 2020

Chromosome 3 duplication q21 leads to qter deletion p25 leads to pter syndrome in children of carriers of a pericentric inversion inv(3) (p25q21)

1 reference

12 December 2020

Frequency and genetic effect of 1qh plus

1 reference

12 December 2020

Inherited pericentric inversion of chromosome no. 2 with Robertsonian translocation (13q 14q) resulting in trisomy for chromosome 13q

1 reference

12 December 2020

Variant chromosome 3 (inv3) in normal newborns and their parents, and in children with mental retardation

1 reference

12 December 2020

Nonrandom distribution of chromosome breaks in cultured lymphocytes of normal subjects

1 reference

12 December 2020

Comparison of the karyotype of the orangutan (Pongo pygmaeus) to those of man, chimpazee, and gorilla

1 reference

12 December 2020

Retinoblastoma and transmission of balanced chromosomal modifications

1 reference

12 December 2020

Ectodermal dysplasia in females and inversion of chromosome 9

1 reference

12 December 2020

High resolution of a small pericentric inversion of chromosome 11.

1 reference

12 December 2020

Human chromosome polymorphism and congenital malformations

1 reference

12 December 2020

Current aspects of evolution genetics

1 reference

12 December 2020

Supernumerary small chromosomal anomaly: report of three cases including one with a familial inversion of chromosome 5

1 reference

12 December 2020

Heterozygosity and homozygosity for a pericentric inversion of human chromosone 3

1 reference

12 December 2020

A dynamic study in two new cases of X chromosome translocations

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00293869

1 reference

PubMed ID

6389316

Dimensions Publication ID

4 August 2017

0 references

1 reference

PubMed ID

6389316