(Q36424466)

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Characterization of a set of X-linked sequences and of a panel of somatic cell hybrids useful for the regional mapping of the human X chromosome

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Europe PubMed Central

PubMed publication ID

14 August 2017

Characterization of a set of X-linked sequences and of a panel of somatic cell hybrids useful for the regional mapping of the human X chromosome (English)

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

author name string

I Oberlé

1

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14 August 2017

G Camerino

2

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PubMed publication ID

14 August 2017

C Kloepfer

3

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14 August 2017

J P Moisan

4

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14 August 2017

K H Grzeschik

5

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PubMed publication ID

14 August 2017

B Hellkuhl

6

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PubMed publication ID

14 August 2017

M C Hors-Cayla

7

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14 August 2017

N Van Cong

8

1 reference

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14 August 2017

D Weil

9

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14 August 2017

J L Mandel

10

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14 August 2017

publication date

1 January 1986

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14 August 2017

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Europe PubMed Central

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14 August 2017

72

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14 August 2017

1

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14 August 2017

43-49

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Europe PubMed Central

PubMed publication ID

14 August 2017

Construction of a genetic linkage map in man using restriction fragment length polymorphisms

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Assignment of a structural gene for beta-glucuronidase to human chromosome C7.

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The glyceraldehyde 3 phosphate dehydrogenase gene family: structure of a human cDNA and of an X chromosome linked pseudogene; amazing complexity of the gene family in mouse

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12 December 2020

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Rapid and efficient cosmid cloning

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12 December 2020

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Isolation and characterization of human random cDNA clones homologous to DNA from the X chromosome

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12 December 2020

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A strategy to reveal high-frequency RFLPs along the human X chromosome

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12 December 2020

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Toward a complete linkage map of the human X chromosome: regional assignment of 16 cloned single-copy DNA sequences employing a panel of somatic cell hybrids

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Further data on the cytologic mapping of the human X chromosome with man-mouse cell hybrids

1 reference

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Extensive DNA sequence homologies between the human Y and the long arm of the X chromosome

1 reference

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12 December 2020

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Actin-like sequences are present on human X and Y chromosomes

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12 December 2020

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Molecular genetics of human serum albumin: restriction enzyme fragment length polymorphisms and analbuminemia

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Report of the Committee on Human Gene Mapping by Recombinant DNA Techniques

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A polymorphic DNA marker genetically linked to Huntington's disease

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Cloning of a representative genomic library of the human X chromosome after sorting by flow cytometry

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12 December 2020

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Genetic mapping of the human X chromosome by using restriction fragment length polymorphisms

1 reference

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Identification of a de novo chromosome rearrangement in a man-mouse hybrid clone and its bearing on the cytological map of the human X chromosome

1 reference

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A new MspI restriction fragment length polymorphism in the hemophilia B locus

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12 December 2020

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Regional localization of the genes for human LDHb, TPI, ENO2, PepB, PGK, alphaGALa, HGPRT, G6PD by interspecific hybridization (author's transl)

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12 December 2020

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15 Detection of specific RNAs or specific fragments of DNA by fractionation in gels and transfer to diazobenzyloxymethyl paper

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Regional localization on the human X chromosome and polymorphism of the coagulation factor IX gene (hemophilia B locus).

1 reference

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12 December 2020

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Localization of MPI, PKM2, IDHM, and the alpha subunit of hexosaminidase (HEXA) to the q21 leads to qter region of human chromosome 15

1 reference

https://pubmed.ncbi.nlm.nih.gov/3002952

12 December 2020

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Restriction sites containing CpG show a higher frequency of polymorphism in human DNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/3002952

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Differential nuclease sensitivity of the ovalbumin and β-globin chromatin regions in erythrocytes and oviduct cells of laying hen

1 reference

https://pubmed.ncbi.nlm.nih.gov/3002952

12 December 2020

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Homologies between X and Y chromosomes detected by DNA probes: localisation and evolution

1 reference

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12 December 2020

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The telomeric region of the human X chromosome long arm: presence of a highly polymorphic DNA marker and analysis of recombination frequency

1 reference

https://pubmed.ncbi.nlm.nih.gov/3002952

12 December 2020

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Assignment of the haemophilia B (factor IX) locus to the q26-qter region of the X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/3002952

12 December 2020

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A new era in mammalian gene mapping: somatic cell genetics and recombinant DNA methodologies

1 reference

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12 December 2020

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Carrier detection of Hemophilia B by using a restriction site polymorphism associated with the coagulation Factor IX gene

1 reference

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Different patterns of X chromosome inactivity in lymphocytes and fibroblasts of a human balanced X;autosome translocation

1 reference

https://pubmed.ncbi.nlm.nih.gov/3002952

12 December 2020

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Identification of human RNA transcripts among heterogeneous nuclear RNA from man-mouse somatic cell hybrids

1 reference

https://pubmed.ncbi.nlm.nih.gov/3002952

12 December 2020

based on heuristic

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The human genes for hemophilia A and hemophilia B flank the X chromosome fragile site at Xq27.3.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3002952

12 December 2020

based on heuristic

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DNA sequence variants in the G gamma-, A gamma-, delta- and beta-globin genes of man

1 reference

https://pubmed.ncbi.nlm.nih.gov/3002952

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A DNA fragment from the human X chromosome short arm which detects a partially homologous sequence on the Y chromosomes long arm.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3002952

12 December 2020

based on heuristic

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Localization by in situ hybridization of the coagulation factor IX gene and of two polymorphic DNA probes with respect to the fragile X site

1 reference

https://pubmed.ncbi.nlm.nih.gov/3002952

12 December 2020

based on heuristic

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Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/3002952

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Regional assignment of arylsulfatase A, mitochondrial aconitase and NADH-cytochrome b5 reductase by somatic cell hybridization

1 reference

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12 December 2020

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DNA methylation: organ specific variations in the methylation pattern within and around ovalbumin and other chicken genes

1 reference

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Familial t(X;2) (p223;q323) with partial trisomy 2q and male and female balanced carriers

1 reference

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12 December 2020

based on heuristic

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Regional localization of the genes for human HEXB. PGK, GALA. HPRT, G6PD by somatic cell hybridization

1 reference

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12 December 2020

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DNA restriction fragment length polymorphisms and heterozygosity in the human genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/3002952

12 December 2020

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Localization of DNA sequences in region Xp21 of the human X chromosome: search for molecular markers close to the Duchenne muscular dystrophy locus.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3002952

12 December 2020

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An estimate of unique DNA sequence heterozygosity in the human genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/3002952

12 December 2020

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[Localization of the LDHA-GST3-ESA4 synthetic group on human chromosome 11. Analyses of the classic man-rodent hybrids and of a new type (not adhering to the wall)]

1 reference

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First trimester prenatal diagnosis of adrenoleukodystrophy by determination of very long chain fatty acid levels and by linkage analysis to a DNA probe

1 reference

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Genetic screening for hemophilia A (classic hemophilia) with a polymorphic DNA probe

1 reference

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Genetic analysis of the fragile-X mental retardation syndrome with two flanking polymorphic DNA markers

1 reference

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12 December 2020

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1 reference

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Isolation and characterization of cDNA clones for human skeletal muscle α actin

1 reference

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Regional localization of the human factor IX gene by molecular hybridization

1 reference

https://pubmed.ncbi.nlm.nih.gov/3002952

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs

1 reference

https://pubmed.ncbi.nlm.nih.gov/3002952

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Extensive sequence homologies between Y and other human chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/3002952

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal male

1 reference

https://pubmed.ncbi.nlm.nih.gov/3002952

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00278816

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

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