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Trisomy 13 and Rubinstein-Taybi syndrome.

Initial diagnosis of Rubinstein-Taybi syndrome was made in an infant with a prominent nose and broad thumbs and first toes. However, due to the presence of other anomalies such as low-set, malformed ears, anti-mongoloid slant of the eyes, colobomata of the iris, and cleft palate, cytogenetic studies...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Garcia, F P, Hsu, L Y, Fox, H, Gribetz, D
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 1975
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC1013239/
https://ncbi.nlm.nih.gov/pubmed/1121015
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