(Q41444965)

English

Analysis of linkage relationships between genetic markers around the fragile X locus with special reference to the daughters of normal transmitting males

scientific article published on September 1986

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

30 September 2017

Analysis of linkage relationships between genetic markers around the fragile X locus with special reference to the daughters of normal transmitting males (English)

1 reference

Europe PubMed Central

PubMed publication ID

30 September 2017

author name string

R M Winter

1

1 reference

Europe PubMed Central

PubMed publication ID

30 September 2017

M E Pembrey

2

1 reference

Europe PubMed Central

PubMed publication ID

30 September 2017

publication date

1 September 1986

1 reference

Europe PubMed Central

PubMed publication ID

30 September 2017

1 reference

Europe PubMed Central

PubMed publication ID

30 September 2017

74

1 reference

Europe PubMed Central

PubMed publication ID

30 September 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

30 September 2017

93-97

1 reference

Europe PubMed Central

PubMed publication ID

30 September 2017

https://scigraph.springernature.com/pub.10.1007/bf00278793

0 references

A gradient of sex linkage in the pseudoautosomal region of the human sex chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/3463533

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/3463533

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/3463533

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/3463533

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The genetic distance between the coagulation factor IX gene and the locus for the fragile X syndrome: clinical implications

1 reference

https://pubmed.ncbi.nlm.nih.gov/3463533

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage analysis of X-linked mental retardation with and without fragile-X using factor IX gene probe

1 reference

https://pubmed.ncbi.nlm.nih.gov/3463533

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Further segregation analysis of the fragile X syndrome with special reference to transmitting males

1 reference

https://pubmed.ncbi.nlm.nih.gov/3463533

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage and recombination between fragile X-linked mental retardation and the factor IX gene.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3463533

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transmission of the marker X syndrome trait by unaffected males: conclusions from studies of large families.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3463533

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/3463533

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA linkage studies in the fragile X syndrome suggest genetic heterogeneity

1 reference

https://pubmed.ncbi.nlm.nih.gov/3463533

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/3463533

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A premutation that generates a defect at crossing over explains the inheritance of fragile X mental retardation

1 reference

https://pubmed.ncbi.nlm.nih.gov/3463533

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00278793

1 reference

Europe PubMed Central

PubMed publication ID

30 September 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

30 September 2017

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q41444965&oldid=2097801178"