(Q52075728)

English

Localization of the gene for a syndrome of X-linked skeletal dysplasia and mental retardation to Xq27-qter.

scientific article published in February 1987

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scholarly article

1 reference

Europe PubMed Central

21 April 2018

http://europepmc.org/abstract/MED/3469136

Localization of the gene for a syndrome of X-linked skeletal dysplasia and mental retardation to Xq27-qter. (English)

1 reference

Europe PubMed Central

21 April 2018

http://europepmc.org/abstract/MED/3469136

author name string

S R Dlouhy

1

1 reference

Europe PubMed Central

21 April 2018

http://europepmc.org/abstract/MED/3469136

J C Christian

2

1 reference

Europe PubMed Central

21 April 2018

http://europepmc.org/abstract/MED/3469136

J L Haines

3

1 reference

Europe PubMed Central

21 April 2018

http://europepmc.org/abstract/MED/3469136

P M Conneally

4

1 reference

Europe PubMed Central

21 April 2018

http://europepmc.org/abstract/MED/3469136

M E Hodes

5

1 reference

Europe PubMed Central

21 April 2018

http://europepmc.org/abstract/MED/3469136

publication date

1 February 1987

1 reference

Europe PubMed Central

21 April 2018

http://europepmc.org/abstract/MED/3469136

1 reference

Europe PubMed Central

21 April 2018

http://europepmc.org/abstract/MED/3469136

75

1 reference

Europe PubMed Central

21 April 2018

http://europepmc.org/abstract/MED/3469136

136-139

1 reference

Europe PubMed Central

21 April 2018

http://europepmc.org/abstract/MED/3469136

2

1 reference

Europe PubMed Central

21 April 2018

http://europepmc.org/abstract/MED/3469136

https://scigraph.springernature.com/pub.10.1007/bf00591074

0 references

Strategies for multilocus linkage analysis in humans

1 reference

https://pubmed.ncbi.nlm.nih.gov/3469136

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A familial syndrome of short stature associated with facial dysplasia and genital anomalies

1 reference

https://pubmed.ncbi.nlm.nih.gov/3469136

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/3469136

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital familial testicular deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/3469136

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The FG syndrome: Further characterization, report of a third family, and of a sporadic case

1 reference

https://pubmed.ncbi.nlm.nih.gov/3469136

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Studies of malformation syndromes of man 33: the FG syndrome. An X-linked recessive syndrome of multiple congenital anomalies and mental retardation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3469136

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic mapping of DNA segments relative to the locus for the fragile-X syndrome at Xq27.3.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3469136

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage studies of X-linked mental retardation: high frequency of recombination in the telomeric region of the human X chromosome (fragile site/linkage/recombination/X chromosome).

1 reference

https://pubmed.ncbi.nlm.nih.gov/3469136

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked skeletal dysplasia with mental retardation

1 reference

https://pubmed.ncbi.nlm.nih.gov/3469136

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Assignment of the gene for dyskeratosis congenita to Xq28

1 reference

https://pubmed.ncbi.nlm.nih.gov/3469136

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The genetic linkage map of the human X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/3469136

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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/3469136

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Conference report: International Workshop on the fragile X and X-linked mental retardation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3469136

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA banking: the effects of storage of blood and isolated DNA on the integrity of DNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/3469136

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00591074

1 reference

Europe PubMed Central

21 April 2018

http://europepmc.org/abstract/MED/3469136

1 reference

Europe PubMed Central

21 April 2018

http://europepmc.org/abstract/MED/3469136

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