Article
High frequency of BRCA1/2 germline mutations in 42 Belgian families with a small number of symptomatic subjects.
Journal of medical genetics - 1 Apr 1999
Goelen G, Teugels E, Bonduelle M, Neyns B, De Grève J
Abstract excerpt
AIM: The initial risk assessments for BRCA1/2 mutation carriers and estimates of carrier frequencies were based on extended pedigrees with a large number of symptomatic subjects. When counselling based on BRCA gene mutation analysis was initiated, we faced requests for counselling mostly from members of small families with only two or three affected members. We report on the likelihood of finding a BRCA mutation...
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