Chromosome Break Point in a Female Infant with the Cri-du-chat Syndrome
1977 Volume 17 Issue 1 Pages 63-65
Details
1977 Volume 17 Issue 1 Pages 63-65
A female infant diagnosed as the cri-du-chat syndrome showed a short arm deletion of chromosome 5. Her karyotype was a 46,XX,del (5) (p14). Both the phenotype and karyotype of her parents were normal.
