Accurate diagnosis of carriers of deletions and duplications in Duchenne/Becker muscular dystrophy by fluorescent dosage analysis.-Reference-Cited by-同舟云学术

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

Published:1996-07-01 Issue:7 Volume:33 Page:550-558
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Yau S C,Bobrow M,Mathew C G,Abbs S J

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference32 articles.

1. Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy;Hodgson, S.V.; Hart, K.; Abbs, S.,1989

2. The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion;Koenig, M.; Beggs, A.H.; Moyer, M.;Am _ Hunm Genet,1989

3. Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of;JT, Den Dunnen; PM, Grootscholten; E, Bakker;Am Humn Genet; cases reveals 115 deletions and 13 duplication,1989

4. A convenient multiplex PCR system for the detection of dystrophin gene deletions: a comparative analysis with cDNA hybridisation reveals mistypings by both methods;Abbs, S.; Yau, S.C.; Clark, S.; Mathew, C.G.; Bobrow, M.;]fMed Genet,1991

5. Report on the 16th ENMC workshop -carrier diagnosis of Duchenne and Becker muscular dystrophy;Abbs, S.; Bobrow, M.;Neuromusc Disord,1993

Cited by 143 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Copy Number Variation: Methods and Clinical Applications;Applied Sciences;2021-01-16

2. Functional evidence (II) protein and enzyme function;Clinical DNA Variant Interpretation;2021

3. An Overview of DNA Analytical Methods;Methods in Molecular Biology;2018-12-12

4. Muscular Dystrophies;Myopathology;2018-09-25

5. A new mutation of the SCGA gene is the cause of a late onset mild phenotype limb girdle muscular dystrophy type 2D with axial involvement;Neuromuscular Disorders;2018-08