Obstet Gynecol. 1977 Feb;49(2):251-3.

Chromosome 6/15 translocation with multiple congenital anomalies.

Abstract

A female infant with multiple congenital anomalies was found to have an abnormal karyotype: 45,XX,--6,--15, +t (6;15). Precise identification of the translocation was made by trypsin-Giemsa banding technic. The congenital malformations include hypertelorism, microphthalmia, beak nose, low-set ears, cleft palate, micrognathia, simian crease, hypertrichosis, and low hairline. The unbalanced translocation is apparently responsible for the abnormal phenotype.

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Chromosome 6/15 translocation with multiple congenital anomalies.
Chromosome 6/15 translocation with multiple congenital anomalies.
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Chromosome 6/15 translocation with multiple congenital anomalies.

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