(Q41347840)

29 September 2017

title

Dissociation between mental retardation and fragile site expression in a family with fragile X-linked mental retardation (English)

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29 September 2017

M A Voelckel

1

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29 September 2017

M G Mattei

2

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29 September 2017

C N'Guyen

3

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29 September 2017

N Philip

4

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29 September 2017

F Birg

5

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29 September 2017

J F Mattei

6

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29 September 2017

publication date

1 December 1988

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29 September 2017

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29 September 2017

volume

80

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29 September 2017

issue

4

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29 September 2017

page(s)

375-378

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The prenatal detection of the fragile X chromosome: review of recent experience

29 September 2017

cites work

1 reference

12 December 2020

Autosomal suppressor gene for fragile-X: an hypothesis

1 reference

12 December 2020

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

1 reference

12 December 2020

Expression in lymphocyte and fibroblast culture of the fragile X chromosome: A new technical approach

1 reference

12 December 2020

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

1 reference

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.

1 reference

12 December 2020

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

1 reference

12 December 2020

A new genetic model for the fragile X syndrome involving an autosomal suppressor gene--comments on the paper by M.H. Israel

1 reference

12 December 2020

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

1 reference

12 December 2020

Detection of specific sequences among DNA fragments separated by gel electrophoresis

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

Population genetics implications of the premutation hypothesis for the generation of the fragile X mental retardation gene

1 reference

12 December 2020

On the gates of hell and a most unusual gene

1 reference

12 December 2020

Somatic cell hybrid studies of fragile (X) expression in a carrier female and transmitting male

1 reference

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.

1 reference

12 December 2020

Analysis of the fragile-X chromosome: localization and detection of the fragile site in high resolution preparations

1 reference

12 December 2020

Phenotypic variation in male-transmitted fragile X: genetic inferences.

1 reference

12 December 2020

The fragile X chromosome.

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

Proposed mechanism of inheritance and expression of the human fragile-X syndrome of mental retardation

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

Large scale physical mapping in the q27 region of the human X chromosome: the coagulation factor IX gene and the mcf.2 transforming sequence are separated by at most 270 kilobase pairs and are surrounded by several 'HTF islands'.

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/BF00273654

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Dimensions Publication ID

29 September 2017

1042416004

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