(Q52252495)

28 April 2018

title

Multilocus analysis of the fragile X syndrome. (English)

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28 April 2018

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8

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author name string

W T Brown

1

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28 April 2018

A Gross

2

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28 April 2018

C Chan

3

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28 April 2018

E C Jenkins

4

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J L Mandel

5

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28 April 2018

I Oberlé

6

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28 April 2018

B Arveiler

7

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28 April 2018

S Thibodeau

9

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R Hagerman

10

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28 April 2018

publication date

1 March 1988

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28 April 2018

published in

Human Genetics

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28 April 2018

volume

78

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28 April 2018

page(s)

201-205

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28 April 2018

issue

3

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28 April 2018

https://scigraph.springernature.com/pub.10.1007/bf00291662

exact match

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cites work

Further evidence for genetic heterogeneity in the fragile X syndrome.

1 reference

12 December 2020

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

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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).

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12 December 2020

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

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12 December 2020

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

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12 December 2020

The genetic linkage map of the human X chromosome

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12 December 2020

The fragile X syndrome in a large family. III. Investigations on linkage of flanking DNA markers with the fragile site Xq27.

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12 December 2020

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

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12 December 2020

Genetic heterogeneity of X-linked mental retardation with fragile X. Association of tight linkage to factor IX and incomplete penetrance in males.

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12 December 2020

Mapping of DNA markers close to the fragile site on the human X chromosome at Xq27.3.

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12 December 2020

RFLP for linkage analysis of fragile X syndrome

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12 December 2020

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

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Physical mapping of the factor VIII gene proximal to two polymorphic DNA probes in human chromosome band Xq28: implications for factor VIII gene segregation analysis

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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

Recombination between the fragile site Xq27 and the gene for coagulation factor IX

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12 December 2020

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

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12 December 2020

Polymorphic DNA markers in prenatal diagnosis of fragile X syndrome

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12 December 2020

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

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12 December 2020

Recombination between the factor VIII gene and the DXS52 locus gives the most probable genetic order as centromere-fra(X)-DXS15-DXS52-F8C-telomere

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12 December 2020

Easy calculations of lod scores and genetic risks on small computers

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12 December 2020

Multipoint genetic mapping of the Xq26-q28 region in families with fragile X mental retardation and in normal families reveals tight linkage of markers in q26-q27.

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12 December 2020

Efficient isolation of X chromosome-specific single-copy probes from a cosmid library of a human X/hamster hybrid-cell line: mapping of new probes close to the locus for X-linked mental retardation

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12 December 2020

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

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12 December 2020

DNA linkage studies in the fragile X syndrome suggest genetic heterogeneity

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12 December 2020

An assessment of the use of flanking DNA markers for fra(X) syndrome carrier detection and prenatal diagnosis

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12 December 2020

Genetic linkage heterogeneity in the fragile X syndrome

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12 December 2020

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

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12 December 2020

Identifiers

DOI

10.1007/BF00291662

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28 April 2018

PubMed ID

3162224

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28 April 2018