Loading...

Carrier detection and prenatal diagnosis in X linked muscular dystrophy using restriction fragment length polymorphisms.

With the aim of offering carrier detection, genetic counselling, and prenatal diagnosis to as many families with Duchenne (DMD) and Becker (BMD) muscular dystrophy as possible, we used available DNA probes to determine the usefulness of the RFLP approach. We report in detail the risks calculated usi...

Fuld beskrivelse

Na minha lista:
Bibliografiske detaljer
Main Authors: Lindlöf, M, Kääriäinen, H, Davies, K E, de la Chapelle, A
Format: Artigo
Sprog:Inglês
Udgivet: 1986
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1049838/
https://ncbi.nlm.nih.gov/pubmed/2879928
Tags: Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!