(Q56797967)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3009302%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

title

Assignment of the gene for dyskeratosis congenita to Xq28 (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3009302%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

main subject

dyskeratosis congenita

1 reference

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3009302%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

author name string

J M Connor

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3009302%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

F C Gray

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3009302%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

L A Pirrit

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3009302%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

N A Affara

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3009302%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

publication date

1 April 1986

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3009302%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3009302%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

volume

72

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3009302%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

page(s)

348-351

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3009302%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3009302%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/bf00290963

8 October 2019

exact match

0 references

cites work

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

1 reference

12 December 2020

Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I

1 reference

12 December 2020

X-linked Dyskeratosis Congenita With Pancytopenia

1 reference

12 December 2020

Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies

1 reference

12 December 2020

Localization of loci for hypoxanthine phosphoribosyltransferase and glucose-6-phosphate dehydrogenase and biochemical evidence of nonrandom X chromosome expression from studies of a human X-autosome translocation

1 reference

12 December 2020

Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants

1 reference

12 December 2020

Genetic mapping: X chromosome

1 reference

12 December 2020

Report of the Committee on the Genetic Constitution of the X and Y Chromosomes

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Linkage disequilibrium for two X-linked genes in Sardinia and its bearing on the statistical mapping of the human X chromosome

1 reference

12 December 2020

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

1 reference

12 December 2020

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

12 December 2020

Dyskeratosis congenita. Report of a large kindred

1 reference

12 December 2020

A cytological map of the human X chromosome--evidence for non-random recombination

1 reference

12 December 2020

Construction of linkage maps with DNA markers for human chromosomes.

1 reference

12 December 2020

Dyskeratosis congenita: clinical features and genetic aspects. Report of a family and review of the literature

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00290963

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3009302%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

1 reference