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Partial duplication of chromosome 8p: Report of 5 patients and review of literature
Egyptian Journal of Medical Human Genetics [The]. 2007; 8 (2): 199-208
em Inglês | IMEMR (Mediterrâneo Oriental) | ID: emr-82408
Biblioteca responsável: EMRO
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





Índice: IMEMR (Mediterrâneo Oriental) Assunto principal: Fenótipo / Literatura de Revisão como Assunto / Aberrações Cromossômicas / Análise Citogenética / Deficiência Intelectual Limite: Feminino / Humanos / Masculino Idioma: Inglês Revista: Egypt. J. Med. Hum. Genet. Ano de publicação: 2007