(Q37686181)

English

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

scientific article published on May 1985

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scholarly article

1 reference

Europe PubMed Central

22 August 2017

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

1 reference

Europe PubMed Central

22 August 2017

author name string

I Oberlé

1

1 reference

Europe PubMed Central

22 August 2017

D Drayna

2

1 reference

Europe PubMed Central

22 August 2017

G Camerino

3

1 reference

Europe PubMed Central

22 August 2017

R White

4

1 reference

Europe PubMed Central

22 August 2017

J L Mandel

5

1 reference

Europe PubMed Central

22 August 2017

language of work or name

0 references

publication date

1 May 1985

1 reference

Europe PubMed Central

22 August 2017

Proceedings of the National Academy of Sciences of the United States of America

1 reference

Europe PubMed Central

22 August 2017

82

1 reference

Europe PubMed Central

22 August 2017

2824-2828

1 reference

Europe PubMed Central

22 August 2017

9

1 reference

Europe PubMed Central

22 August 2017

Further scoring types in sequential linkage tests, with a critical review of autosomal and partial sex linkage in man.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=397658

23 August 2017

A highly polymorphic locus in human DNA

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=397658

23 August 2017

Adrenoleukodystrophy: evidence for X linkage, inactivation, and selection favoring the mutant allele in heterozygous cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=397658

23 August 2017

Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=397658

23 August 2017

Cytological mapping of the human glucose-6-phosphate dehydrogenase gene distal to the fragile-X site suggests a high rate of meiotic recombination across this site

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=397658

23 August 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=397658

23 August 2017

Studies on hemophilia A in Sardinia bearing on the problems of multiple allelism, carrier detection, and differential mutation rate in the two sexes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=397658

23 August 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=397658

23 August 2017

Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=397658

23 August 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=397658

23 August 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=397658

23 August 2017

A polymorphic DNA marker genetically linked to Huntington's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=397658

23 August 2017

Beta-globin locus is linked to the parathyroid hormone (PTH) locus and lies between the insulin and PTH loci in man

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=397658

23 August 2017

A three-allele restriction-fragment-length polymorphism at the hypoxanthine phosphoribosyltransferase locus in man.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=397658

23 August 2017

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://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=397658

23 August 2017

Multiple DNA fragment polymorphisms associated with immunoglobulin mu chain switch-like regions in man.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=397658

23 August 2017

Nonrandom association of polymorphic restriction sites in the β-globin gene cluster

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=397658

23 August 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=397658

23 August 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=397658

14 September 2017

Brief report: linkage between G6PD and fragile-X syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=397658

23 June 2018

A clinically useful DNA probe closely linked to haemophilia A

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=397658

23 June 2018

Characterisation and use of an intragenic polymorphic marker for detection of carriers of haemophilia B (factor IX deficiency).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=397658

23 June 2018

Chiasma distribution at diakinesis in the normal human male

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=397658

23 June 2018

Construction of linkage maps with DNA markers for human chromosomes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=397658

23 June 2018

The highly polymorphic region near the human insulin gene is composed of simple tandemly repeating sequences.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=397658

1 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=397658

1 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=397658

1 September 2018

Cloned human phenylalanine hydroxylase gene allows prenatal diagnosis and carrier detection of classical phenylketonuria

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=397658

1 September 2018

Model for antenatal diagnosis of β-thalassaemia and other monogenic disorders by molecular analysis of linked DNA polymorphisms

1 reference

https://pubmed.ncbi.nlm.nih.gov/2986139

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evolution of the hemoglobin S and C genes in world populations

1 reference

https://pubmed.ncbi.nlm.nih.gov/2986139

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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/2986139

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage relationship of a cloned DNA sequence on the short arm of the X chromosome to Duchenne muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/2986139

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic mapping: X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2986139

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regional localization of the human factor IX gene by molecular hybridization

1 reference

https://pubmed.ncbi.nlm.nih.gov/2986139

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.82.9.2824

1 reference

Europe PubMed Central

22 August 2017

1985PNAS...82.2824O

0 references

1 reference

Europe PubMed Central

22 August 2017

1 reference

Europe PubMed Central

22 August 2017

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