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Pseudohermaphroditism with clinical features of trisomy 19 in an infant trisomic for parts of chromosomes 16 and 18: 47,XY,der(18),t(16;18)(p12;q11)mat.

The case is presented of an infant who was diagnosed clinically as trisomy 18 with pseudohermaphroditism. Cytogenetic studies revealed an extra chromosome which represented a translocation chromosome derived from a balanced, reciprocal translocation between chromosomes 16 and 18: [der(18),t(16;18)(p...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Stern, L M, Mureh, A R
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 1975
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC1013296/
https://ncbi.nlm.nih.gov/pubmed/1177285
Etiketak: Etiketa erantsi
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