12;14 translocation in Coffin Siris syndrome.

Patel, Z M; Mulye, V R; Raghavan, K; Shah, S B

Patel, Z M; Mulye, V R; Raghavan, K; Shah, S B.

Indian Pediatr ; 1987 May; 24(5): 435-8

Article in English | IMSEAR | ID: sea-13725

Subject(s)

Chromosomes, Human, Pair 12; Chromosomes, Human, Pair 14; Facial Expression; Female; Humans; Infant, Newborn; Karyotyping; Intellectual Disability/genetics; Nails, Malformed/genetics; Syndactyly/genetics; Syndrome; Translocation, Genetic

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Full text: Available Index: IMSEAR (South-East Asia) Main subject: Syndrome / Translocation, Genetic / Chromosomes, Human, Pair 12 / Chromosomes, Human, Pair 14 / Female / Humans / Infant, Newborn / Syndactyly / Facial Expression / Karyotyping Language: English Journal: Indian Pediatr Year: 1987 Type: Article

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