(Q41376009)

30 September 2017

1 reference

title

Prenatal diagnosis of Duchenne and Becker muscular dystrophy (English)

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30 September 2017

Abbs S

1

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30 September 2017

language of work or name

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1 December 1996

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30 September 2017

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30 September 2017

volume

16

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30 September 2017

issue

13

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30 September 2017

page(s)

1187-1198

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Analysis of quantitative PCR for the diagnosis of deletion and duplication carriers in the dystrophin gene

30 September 2017

cites work

1 reference

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A convenient multiplex PCR system for the detection of dystrophin gene deletions: a comparative analysis with cDNA hybridisation shows mistypings by both methods

21 January 2018

1 reference

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Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction

21 January 2018

1 reference

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Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification

21 January 2018

1 reference

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Transcription of the dystrophin gene in human muscle and non-muscle tissue

21 January 2018

1 reference

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Pregnancy after embryo biopsy and coamplification of DNA from X and Y chromosomes

21 January 2018

1 reference

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On the origin of deletions and point mutations in Duchenne muscular dystrophy: most deletions arise in oogenesis and most point mutations result from events in spermatogenesis

21 January 2018

1 reference

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The rate of spontaneous mutation of a human gene

21 January 2018

1 reference

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Pregnancies from biopsied human preimplantation embryos sexed by Y-specific DNA amplification

21 January 2018

1 reference

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Dystrophin: the protein product of the Duchenne muscular dystrophy locus

21 January 2018

1 reference

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Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals

21 January 2018

1 reference

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An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus

21 January 2018

1 reference

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Point mutations in the dystrophin gene

21 January 2018

1 reference

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Analysis of dystrophin expression after activation of myogenesis in amniocytes, chorionic-villus cells, and fibroblasts. A new method for diagnosing Duchenne's muscular dystrophy.

21 January 2018

1 reference

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Prenatal diagnosis of Duchenne muscular dystrophy using a single fetal nucleated erythrocyte in maternal blood.

21 January 2018

1 reference

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Isolating fetal cells in maternal circulation for prenatal diagnosis.

21 January 2018

1 reference

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Expression of an X-linked muscular dystrophy in a female due to translocation involving Xp21 and non-random inactivation of the normal X chromosome

21 January 2018

1 reference

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Accurate diagnosis of carriers of deletions and duplications in Duchenne/Becker muscular dystrophy by fluorescent dosage analysis

21 January 2018

1 reference

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Whole genome amplification from a single cell: implications for genetic analysis

21 January 2018

1 reference

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Accurate assessment of intragenic recombination frequency within the Duchenne muscular dystrophy gene

21 January 2018

1 reference

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Direct diagnosis of carriers of point mutations in Duchenne muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291097-0223%28199612%2916%3A13%3C1187%3A%3AAID-PD94%3E3.0.CO%3B2-2

Germline mosaicism and Duchenne muscular dystrophy mutations

21 January 2018

1 reference

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Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291097-0223%28199612%2916%3A13%3C1187%3A%3AAID-PD94%3E3.0.CO%3B2-2

10.1002/(SICI)1097-0223(199612)16:13<1187::AID-PD94>3.0.CO;2-2

21 January 2018

Identifiers

DOI

1 reference

30 September 2017

1 reference