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Clinical and Molecular Cytogenetic Analysis of a Rare Case of Mosaicism for Partial Trisomy 3p and Partial Trisomy 10q in Humans

✍ Scribed by T. B. Karamysheva; V. G. Matveeva; A. P. Shorina; N. B. Rubtsov

Book ID
110350795
Publisher
SP MAIK Nauka/Interperiodica
Year
2001
Tongue
English
Weight
113 KB
Volume
37
Category
Article
ISSN
1022-7954

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## Abstract An 11‐year‐old girl presented with the phenotype of microcephaly, moderate mental retardation, motor retardation, short stature, strabismus, brachydactyly, and facial dysmorphism. She had undergone surgery for inguinal hernias. Detailed examinations of the heart and other internal organ