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Partial trisomy 15 (dup 15q) syndrome and the need for precision in clinical cytogenetics

โœ Scribed by Frederich Hecht


Book ID
118538592
Publisher
Elsevier Science
Year
1975
Tongue
English
Weight
158 KB
Volume
87
Category
Article
ISSN
1097-6833

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A syndrome of mental retardation and multiple congenital anomalies, including craniosynostosis and overgrowth, was observed in two related individuals from a large kindred. Both of them carried a 15q25.1-qter trisomy associated with a subtle 13qter monosomy resulting from unbalanced segregation of a