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

There are 23 females known with Duchenne or Becker muscular dystrophy (DMD or BMD) who have X;autosome translocations that disrupt the X chromosome within band p21. A female with a t(X;4)(p21;q35) translocation was identified prenatally at routine amniocentesis. At birth, she was found to have a rai...

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Bibliografski detalji
Glavni autori: Bodrug, S E, Roberson, J R, Weiss, L, Ray, P N, Worton, R G, Van Dyke, D L
Format: Artigo
Jezik:Inglês
Izdano: 1990
Teme:
Research Article
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1017179/
https://ncbi.nlm.nih.gov/pubmed/2395160
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