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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...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
में प्रकाशित:J Med Genet
मुख्य लेखकों: Garcia, F P, Hsu, L Y, Fox, H, Gribetz, D
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: BMJ Publishing Group 1975
विषय:
ऑनलाइन पहुंच:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC1013239/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1121015/
https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jmg.12.1.104
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