טוען...

Genetic counselling in facioscapulohumeral muscular dystrophy.

Clinical data are presented from a survey of 41 families with dominantly inherited facioscapulohumeral muscular dystrophy (FSHD) in which over 500 family members were examined, including 168 affected subjects. New mutation could account for six isolated cases. Results suggest that 33% of heterozygot...

תיאור מלא

שמור ב:
מידע ביבליוגרפי
Main Authors: Lunt, P W, Harper, P S
פורמט: Artigo
שפה:Inglês
יצא לאור: 1991
נושאים:
גישה מקוונת:https://ncbi.nlm.nih.gov/pmc/articles/PMC1017051/
https://ncbi.nlm.nih.gov/pubmed/1941962
תגים: הוספת תג
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