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Egyptian Journal of Medical Human Genetics [The]. 2007; 8 (2): 199-208
em Inglês | IMEMR (Mediterrâneo Oriental) | ID: emr-82408

RESUMO

The partial chromosome 8p duplication is a rare syndrome and is associated with a characteristic phenotype, including multiple congenital anomalies and mental retardation of various degrees. However, different outcomes depend on the size and location of the duplicated area. We present clinical and cytogenetic data of 5 Arab patients with de novo inversion duplication of 8p. This report provides additional cases to the growing literature


Assuntos
Humanos , Masculino , Feminino , Fenótipo , Deficiência Intelectual , Análise Citogenética , Literatura de Revisão como Assunto , Aberrações Cromossômicas
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