(Q51965391)

19 April 2018

title

Preimplantation genetic diagnosis of the fragile X syndrome by use of linked polymorphic markers. (English)

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19 April 2018

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Apessos A

1

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19 April 2018

Abou-Sleiman PM

series ordinal

2

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19 April 2018

Harper JC

series ordinal

3

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19 April 2018

Delhanty JD

series ordinal

4

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19 April 2018

publication date

1 June 2001

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19 April 2018

published in

Prenatal Diagnosis

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19 April 2018

volume

21

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19 April 2018

issue

6

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19 April 2018

page(s)

504-511

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19 April 2018

Bibliography on ceroid-lipofuscinoses, II.

cites work

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Fine structure of the human FMR1 gene

21 January 2018

1 reference

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

21 January 2018

1 reference

Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1.

21 January 2018

1 reference

Increased serum FSH in female fragile X premutation carriers with either regular menstrual cycles or on oral contraceptives

21 January 2018

1 reference

A rapid non-enzymatic method for the preparation of HMW DNA from blood for RFLP studies

21 January 2018

1 reference

Haemophilia A diagnosis by analysis of a hypervariable dinucleotide repeat within the factor VIII gene

21 January 2018

1 reference

Studies of FRAXA and FRAXE in women with premature ovarian failure

21 January 2018

1 reference

A human X-Y homologous region encodes "amelogenin"

21 January 2018

1 reference

Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome

21 January 2018

1 reference

Absence of expression of the FMR-1 gene in fragile X syndrome

21 January 2018

1 reference

Characterization of a highly polymorphic dinucleotide repeat 150 KB proximal to the fragile X site

21 January 2018

1 reference

Obstetrical and gynecological complications in fragile X carriers: a multicenter study

21 January 2018

1 reference

Preimplantation diagnosis for Huntington's disease (HD): clinical application and analysis of the HD expansion in affected embryos.

21 January 2018

1 reference

DNA methylation represses FMR-1 transcription in fragile X syndrome

21 January 2018

1 reference

Four STR polymorphisms map to a 500 kb region between DXS15 and DXS134

21 January 2018

1 reference

Fragile X premutation is a significant risk factor for premature ovarian failure: the International Collaborative POF in Fragile X study--preliminary data

21 January 2018

1 reference

Preimplantation diagnosis

21 January 2018

1 reference

21 January 2018

The fragile X syndrome

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Experimental limits of PCR analysis of (CA)n repeat alterations

21 January 2018

1 reference

Mutational analysis of the FMR1 gene in 118 mentally retarded males suspected of fragile X syndrome: absence of prevalent mutations

21 January 2018

1 reference

Human preimplantation development in vitro is not adversely affected by biopsy at the 8-cell stage

21 January 2018

1 reference

A study of the origin of 'shadow bands' seen when typing dinucleotide repeat polymorphisms by the PCR

21 January 2018

1 reference

Successful pregnancy in a fragile X carrier by donor egg

21 January 2018

1 reference

Fluorescent PCR and automated fragment analysis for the clinical application of preimplantation genetic diagnosis of myotonic dystrophy (Steinert's disease)

21 January 2018

1 reference

Prevalence of fragile X syndrome

21 January 2018

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21 January 2018

Identifiers

DOI

10.1002/PD.111

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19 April 2018

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19 April 2018