Prenatal identification of a girl with a t(X;4)(p21;q35) translocation: molecular characterisation, paternal origin, and association with muscular dystrophy.-Reference-Cited by-同舟云学术

Prenatal identification of a girl with a t(X;4)(p21;q35) translocation: molecular characterisation, paternal origin, and association with muscular dystrophy.

Published:1990-07-01 Issue:7 Volume:27 Page:426-432
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Bodrug S E,Roberson J R,Weiss L,Ray P N,Worton R G,Van Dyke D L

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference40 articles.

1. Genetics of Duchenne muscular dystrophy;Worton, R.G.; Thompson, M.W.,1988

2. Craig 1. Muscular dystrophy in girls with X; autosome translocations..7 Med;Boyd, Y.; Buckle, V.; Holt, S.; Munro, E.; Hunter, D.;Genet,1986

3. Cytogenetic heterogeneitv of translocations associated with Duchenne muscular dystrophy;Boyd, Y.; Buckle, V.J.;Clin Genet,1986

4. Long-range restriction map around the Duchenne muscular dystrophy gene;Burmeister, M.; Lehrach, H.;Nature,1986

5. A 10 megabase physical map of human Xp2 1, including the Duchenne muscular dystrophy gene;Burmeister, M.; Monaco, A.P.; Gillard, E.F.;Genomics,1988

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