Trisomy 10p syndrome owing to maternal pericentric inversion.
AUTOR(ES)
Ohba, K
RESUMO
A female infant with karyotype 46,XX,rec(10),dup p inv(10)(p11.2q25.2)mat is presented. She had both duplication of 10p and deletion of distal 10q, but only had the constellation of specific features characteristic of duplication of 10p.
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1017032Documentos Relacionados
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