Three Generations and Six Family Members with a t(13q15q) Chromosome

AUTOR(ES)

Neu, Richard L.

RESUMO

A patient with the clinical features of trisomy 13 without prosencephalic defects and with a 46,XX,15-,t(13q15q)+ karyotype is reported. The translocation chromosome was present in five other phenotypically normal family members and could be traced back to the maternal grandfather.

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