(Q39344794)

11 September 2017

Functional implications of differential chromosome banding (English)

2 references

11 September 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A51585

8 April 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A51585

8 April 2022

author name string

H. Hoehn

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A51585

8 April 2022

publication date

1 September 1975

1 reference

full work available at URL

11 September 2017

language of work or name

English

0 references

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/51585/?tool=EBI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A51585

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/51585/pdf/?tool=EBI

8 April 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A51585

https://europepmc.org/articles/PMC1762823

8 April 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A51585

https://europepmc.org/articles/PMC1762823?pdf=render

8 April 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A51585

American Journal of Human Genetics

8 April 2022

published in

1 reference

11 September 2017

27

1 reference

11 September 2017

5

1 reference

11 September 2017

676-685

1 reference

3 CASES OF PARTIAL DELETION OF THE SHORT ARM OF A 5 CHROMOSOME

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

Study of somatic chromosomes from 9 mongoloid children

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

Deficiency on the short arms of a chromosome No. 4

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

A case of partial 14 trisomy 47,XY,(14q-)+ and translocation t(9p+;14q-) in mother and brother

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

Quinacrine mustard fluorescence of human chromosomes: characterization of unusual translocations

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

Banding analysis of abnormal karyotypes in spontaneous abortion

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

Compositional heterogeneity of human heterochromatin

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

21 monosomy in a retarded female infant

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

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

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

Tentative localization of a Hageman (Factor XII) locus on 7q, probably the 7q35 band

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

A manyfold increase in sister chromatid exchanges in Bloom's syndrome lymphocytes

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

Sister chromatid exchanges, indices of human chromosome damage and repair: detection by fluorescence and induction by mitomycin C.

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

Translocation, t(4qminus;13qplus), in three generations resulting in partial trisomy of the long arm of chromosome 4 in the fourth generation

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

An analysis of the break points of structural rearrangements in man

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

Letter: A new consistent chromosomal abnormality in chronic myelogenous leukaemia identified by quinacrine fluorescence and Giemsa staining

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

Chromosome structure as revealed by a combined chemical and immunochemical procedure

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

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

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

Nonrandom chromosomal abnormalities in hematologic disorders of man

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

Possible role of heterochromatin in human aneuploidy

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

Genetics and human disease

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

The Structure and Function of Chromatin

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

14 September 2017

Autosomal polymorphisms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

Para-nucleolar Position of the Human Y Chromosome in Interphase Nuclei

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

Identification and characterization of heterochromatic regions in the human metaphase and interphase nucleus

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

Preferential location of x-ray induced chromosome breakage in the R-bands of human chromosomes

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

Variation in the nonfluorescent segment of long Y chromosome

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

Partial trisomy of chromosome number 15 identified by trypsin-Giemsa banding

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

Radiation-induced non-random chromosome breakage

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

Abnormalities of human sex chromosomes. I. A ring Y without mosaiciam

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

Assignment by Deletion of Human Red Cell Acid Phosphatase Gene Locus to the Short Arm of Chromosome 2

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

Partial trisomy 8 (8q24) and the trisomy-8 syndrome

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

Down's syndrome. The possibility of a pathogenetic segment on chromosome no. 21.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

Precise identification of various chromosomal abnormalities.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

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

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

Trisomy 12p due to familial t(12p-,6q plus) translocation.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

Different forms of incomplete trisomy 13. Mosaicism and partial trisomy for the proxim

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

Karyotype of the chimpanzee, Pan troglodytes, based on measurements and banding pattern: comparison to the human karyotype

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

Nonrandom distribution of chromosome breaks in Fanconi's anemia

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

Correlation of the fluorescent banding pattern and ultrastructure of a human chromosome

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

The use of distribution functions to describe integrated density profiles of human chromosomes

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

An unbalanced 4q-21q translocation identified by the R but not by the G and Q chromosome banding techniques.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

Nonrandom arrangement of human chromatin: topography of disomic markers X, Y, and 1h plus 1.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

Presumptive direct insertion within chromosome 2 in man

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

High resolution studies on the pattern of induced exchanges in the human karyotype

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

A ring chromosome, diagnosed by quinacrine fluorescence as No. 9, in a mentally retarded girl

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

Evaluation of chromosome errors at the moment of conception

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

Cytogenetics of malignant lymphomas. Studies utilising a Giemsa-banding technique

21 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

Partial trisomy 8: trisomy of the distal part of the long arm of chromosome number 8 plus (8q2) in a severely retarded and malformed girl

21 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762823

A new technic of analysis of the human karyotype

21 August 2018

1 reference

12 December 2020

The relationship between patterns of DNA replication and of quinacrine fluorescence in the human chromosome complement

1 reference

12 December 2020

Polymorphism of the human Y chromosomes: fluorescence microscopic studies on the sites of morphologic variation

1 reference

12 December 2020

Identification of partial 12 trisomy by quinacrine fluorescence

1 reference

12 December 2020

DNA content and DNA-based centromeric index of the 24 human chromosomes

1 reference

12 December 2020

The mechanism of C- and G-banding of chromosomes

1 reference

12 December 2020

[Polymorphism of human constitutive heterochromatin in metaphase chromosome A1]

1 reference

12 December 2020

[Giemsa-R-banding analysis of the trisomy 9p and report of a new case]

1 reference

12 December 2020

[New system of chromosome banding: the T bands (author's transl)]

1 reference

12 December 2020

Identification by fluorescence of two G rings: (46,XY,21r) G deletion syndrome I and (46, XX, 22r) G deletion syndrome II

1 reference

12 December 2020

[Partial trisomy 11q identified by study, with heat controlled denaturation, of the paternal balanced translocation]

1 reference

12 December 2020

Ring chromosome D (13) associated with multiple congenital malformations

1 reference

12 December 2020

Familial balanced translocation t(2; 13) (q32; q33) and partial trisomy 2q

1 reference

12 December 2020

Ring chromosome 8 (46,XY, 8 r) in a boy with debility (author's transl)

1 reference

12 December 2020

A new syndrome resulting from partial trisomy for the distal third of the long arm of chromosome 10

1 reference

12 December 2020

Brother and sister with trisomy 10p: a new syndrome

1 reference

12 December 2020

C 11-D 13-translocation in four generations

1 reference

12 December 2020

4 cases of trisomy for the short arm of chromosome 9. Individualization of a new morbid entity

1 reference

12 December 2020

Observation of the 13-15 chromosome group in a ring (46,XY,15r)

1 reference

12 December 2020

Structural Polymorphism in Chromosome 17

1 reference

12 December 2020

Multiple congenital anomalies associated with a ring 3 chromosome and translocated 3/X chromosome

1 reference

12 December 2020

Ring 1 chromosome and dwarfism—a possible syndrome

1 reference

12 December 2020

Partial trisomy of chromosome 11: a case report

1 reference

12 December 2020

A comparison between quinacrine fluorescence banding and 3H-thymidine incorporation patterns in human chromosomes

1 reference

12 December 2020

Chromosome studies in 5,049 consecutive newborn children

1 reference

12 December 2020

Mapping Human Autosomes: Assignment of the MN Locus to a Specific Segment in the Long Arm of Chromosome No. 2

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

Human Y-chromatin. 3. The nucleolus

1 reference

12 December 2020

New observations on the human and chimpanzee karyotypes. Identification of breakage points of pericentric inversions

1 reference

12 December 2020

A partial trisomy of chromosome 1 in a family with a t(1q-;4q+) translocation

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

Chromosome banding patterns in an infant with 13q minus syndrome

1 reference

12 December 2020

Loss of DNA following C-banding procedures

1 reference

12 December 2020

Trisomy of the short arm of chromosome 17

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

Colored reverse-banding of human chromosomes with acridine orange following alkaline-formalin treatment: densitometric validation and applications

1 reference

12 December 2020

[Effects of pH on the staining of human chromosomes with acridine orange]

1 reference

12 December 2020

A presumptive tetrasomy for the short arm of chromosome 9

1 reference

12 December 2020

Computerized chromosome identification by aid of the quinacrine mustard fluorescence technique

1 reference

12 December 2020

"Cri du Chat" due to a ring-B chromosome

1 reference

12 December 2020

[Partial trisomy 10 due to hereditary translocation t(1;10)(q44;q22)]

1 reference

12 December 2020

Trisomy for short arm of chromosome 20

1 reference

12 December 2020

Probable trisomy 22 identified by fluorescent and trypsin-giemsa banding

1 reference

12 December 2020

Deletion of the long arm of chromosome no. 7: Tentative assignment of the Kidd (Jk) Locus

1 reference

12 December 2020

Ring chromosome 18. 18p-/18q- -deletion-syndrome

1 reference

12 December 2020

Individualized human karyotyping through quantitative analysis

1 reference

12 December 2020

Non-random occurrence of 7–14 translocations in human lymphocyte cultures

1 reference

12 December 2020

TRISOMY OF AUTOSOME 16

1 reference

12 December 2020

Interphase Deoxyribonucleic Acid Condensation, Late Deoxyribonucleic Acid Replication, and Gene Inactivation

1 reference

12 December 2020

Identifiers

1 reference

11 September 2017

1 reference