(Q51003946)

26 March 2018

title

Examination of factors that influence the expansion of the fragile X mutation in a sample of conceptuses from known carrier females. (English)

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26 March 2018

author name string

Sherman SL

series ordinal

1

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26 March 2018

Meadows KL

series ordinal

2

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26 March 2018

Ashley AE

series ordinal

3

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26 March 2018

publication date

1 August 1996

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26 March 2018

American Journal of Medical Genetics Part A

published in

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26 March 2018

volume

64

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26 March 2018

issue

2

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26 March 2018

page(s)

256-260

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26 March 2018

Length of uninterrupted CGG repeats determines instability in the FMR1 gene

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Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

21 January 2018

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Molecular analysis of new mutations for Huntington's disease: intermediate alleles and sex of origin effects.

21 January 2018

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Inheritance of the fragile X syndrome: size of the fragile X premutation is a major determinant of the transition to full mutation

21 January 2018

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Cryptic and polar variation of the fragile X repeat could result in predisposing normal alleles.

21 January 2018

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Affected sibs with fragile X syndrome exhibit an age-dependent decrease in the size of the fragile X full mutation

21 January 2018

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The full mutation in the FMR-1 gene of male fragile X patients is absent in their sperm.

21 January 2018

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Investigation of the twinning rate in families with the fragile X syndrome

21 January 2018

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Collaborative prospective study of the fragile X syndrome: request for participation

21 January 2018

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Sequence analysis of the fragile X trinucleotide repeat: implications for the origin of the fragile X mutation

21 January 2018

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Genotype mosaicism in fragile X fetal tissues

21 January 2018

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Mitotic stability of fragile X mutations in differentiated cells indicates early post-conceptional trinucleotide repeat expansion.

21 January 2018

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Dizygous twinning and premature menopause in fragile X syndrome

21 January 2018

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Characteristics of the transmission of the FMR1 gene from carrier females in a prospective sample of conceptuses

21 January 2018

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Analysis of full fragile X mutations in fetal tissues and monozygotic twins indicate that abnormal methylation and somatic heterogeneity are established early in development

21 January 2018

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Precursor arrays for triplet repeat expansion at the fragile X locus

21 January 2018

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10.1002/(SICI)1096-8628(19960809)64:2<256::AID-AJMG4>3.0.CO;2-S

21 January 2018

Identifiers

DOI

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26 March 2018

1 reference

26 March 2018