Preimplantation genetic diagnosis for fragile X syndrome using multiplex nested PCR. (Q51757362)

11 April 2018

title

Preimplantation genetic diagnosis for fragile X syndrome using multiplex nested PCR. (English)

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3

Dalit Ben Yosef

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author name string

Mira Malcov

1

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Tova Naiman

2

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Ariella Carmon

4

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Nava Mey-Raz

5

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Ami Amit

6

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Israel Vagman

7

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Yuval Yaron

8

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publication date

1 April 2007

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Reproductive BioMedicine Online

published in

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volume

14

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issue

4

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page(s)

515-521

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

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RS46(DXS548) genotyping of reproductive cells: approaching preimplantation testing of the fragile-X syndrome.

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

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The risk of fragile X premutation expansion is lower in carriers detected by general prenatal screening than in carriers from known fragile X families

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Preimplantation genetic diagnosis for single gene disorders: experience with five single gene disorders

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Multiplex nested PCR for preimplantation genetic diagnosis of spinal muscular atrophy.

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Serum concentrations of follicle stimulating hormone may predict premature ovarian failure in FRAXA premutation women

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

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Detection of full fragile X mutation.

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

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Preimplantation genetic diagnosis for fragile Xa syndrome: difficult but not impossible.

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On some technical aspects of direct DNA diagnosis of the fragile X syndrome

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PGD in the lab for triplet repeat diseases - myotonic dystrophy, Huntington's disease and Fragile-X syndrome.

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DNA methylation represses FMR-1 transcription in fragile X syndrome

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Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

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Polar body-based preimplantation diagnosis for X-linked disorders.

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Identifiers

DOI

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11 April 2018

PubMed ID

17425837

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11 April 2018