(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

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scholarly article

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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

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Europe PubMed Central

PubMed publication ID

30 September 2017

1 reference

Europe PubMed Central

PubMed publication ID

30 September 2017

74

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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

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

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0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

30 September 2017

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