De novo deletion of chromosome 9 (9p-) in a child with multiple congenital anomalies and psychomotor retardation.

Murthy, D S; Murthy, S K; Banker, G J; Patel, A J

Murthy, D S; Murthy, S K; Banker, G J; Patel, A J.

Indian Pediatr ; 1991 May; 28(5): 546-9

Article in English | IMSEAR | ID: sea-12911

Subject(s)

Abnormalities, Multiple/diagnosis; Chromosome Aberrations/genetics; Chromosome Deletion; Chromosomes, Human, Pair 9/ultrastructure; Craniofacial Dysostosis/diagnosis; Cryptorchidism/diagnosis; Humans; Infant; Karyotyping; Male; Psychomotor Disorders/diagnosis

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Full text: Available Index: IMSEAR (South-East Asia) Main subject: Psychomotor Disorders / Abnormalities, Multiple / Chromosomes, Human, Pair 9 / Humans / Male / Chromosome Aberrations / Chromosome Deletion / Craniofacial Dysostosis / Cryptorchidism / Infant Language: English Journal: Indian Pediatr Year: 1991 Type: Article

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