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Gonadal dysgenesis in a 46,XY female mosaic for double autosomal trisomies 8 and 21.

The proband was evaluated at 19 years of age because of primary amenorrhoea and, on chromosomal analysis, was found to have a 46,XY karyotype in 75% of her cells and 48,XY, +8, +21 in 25% of her cells. She appeared normal at birth and exhibited normal intellectual and physical development until pube...

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Bibliografski detalji
Glavni autori: Sulewski, J M, Thao-phuong-Dang, Ward, S, Ladda, R L
Format: Artigo
Jezik:Inglês
Izdano: 1980
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1048581/
https://ncbi.nlm.nih.gov/pubmed/6451706
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