(Q41346550)

29 September 2017

title

Linkage heterogeneity and fragile X. (English)

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29 September 2017

J F Clayton

1

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29 September 2017

C M Gosden

series ordinal

2

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29 September 2017

N D Hastie

series ordinal

3

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29 September 2017

H J Evans

series ordinal

4

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29 September 2017

language of work or name

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1 April 1988

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29 September 2017

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29 September 2017

volume

78

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29 September 2017

issue

4

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29 September 2017

page(s)

338-342

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Ten families with fragile X syndrome: linkage relationships with four DNA probes from distal Xq

29 September 2017

cites work

1 reference

12 December 2020

Further evidence for genetic heterogeneity in the fragile X syndrome.

1 reference

12 December 2020

Autosomal suppressor gene for fragile-X: an hypothesis

1 reference

12 December 2020

Evidence against close linkage of the loci for fraXq of Martin-Bell syndrome and for factor IX

1 reference

12 December 2020

Linkage analysis using multiple Xq DNA polymorphisms in normal families, families with the fragile X syndrome, and other families with X linked conditions

1 reference

12 December 2020

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

1 reference

12 December 2020

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

12 December 2020

Analysis of fragile X-mental retardation families using flanking polymorphic DNA probes.

1 reference

12 December 2020

Strategies for multilocus linkage analysis in humans

1 reference

12 December 2020

The marker (X) syndrome: a cytogenetic and genetic analysis.

1 reference

12 December 2020

The genetic linkage map of the human X chromosome

1 reference

12 December 2020

Population incidence and segregation ratios in the Martin-Bell syndrome.

1 reference

12 December 2020

Mutants affecting meiosis in natural populations of Drosophila melanogaster

1 reference

12 December 2020

Linkage analysis and family classification under heterogeneity

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Genetic linkage between X-linked retinitis pigmentosa and DNA probe DXS7 (L1.28): further linkage data, heterogeneity testing, and risk estimation

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

TESTING FOR HETEROGENEITY OF RECOMBINATION FRACTION VALUES IN HUMAN GENETICS

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

A multipoint linkage analysis program for X-linked disorders, with the example of Duchenne muscular dystrophy and seven DNA probes

1 reference

12 December 2020

The female and the fragile X. A study of 144 obligate female carriers.

1 reference

12 December 2020

Mental impairment in Martin-Bell syndrome is probably determined by interaction of several genes: simple explanation of phenotypic differences between unaffected and affected males with the same X chromosome.

1 reference

12 December 2020

Heritable fragile sites on human chromosomes. III. Detection of fra(X)(q27) in males with X-linked mental retardation and in their female relatives

1 reference

12 December 2020

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

1 reference

12 December 2020

DNA linkage studies in the fragile X syndrome suggest genetic heterogeneity

1 reference

12 December 2020

Linkage relationships between X-linked retinitis pigmentosa and nine short-arm markers: exclusion of the disease locus from Xp21 and localization to between DXS7 and DXS14.

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00291731

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Dimensions Publication ID

29 September 2017

1050060264

0 references

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