Chromosome Break Point in a Female Infant with the Cri-du-chat Syndrome

Tsutomu FUKUSHIMA; Kenichi HATA; Kimio NEMOTO; Jin HONDA; Junichi MURAMOTO

doi:10.24540/cgafa.17.1_63

official journal of Congeital Anomalies Research Association of Japan

Online ISSN : 2433-1503
Print ISSN : 0037-2285

Chromosome Break Point in a Female Infant with the Cri-du-chat Syndrome

Tsutomu FUKUSHIMA, Kenichi HATA, Kimio NEMOTO, Jin HONDA, Junichi MURAMOTO

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JOURNAL FREE ACCESS

1977 Volume 17 Issue 1 Pages 63-65

DOI https://doi.org/10.24540/cgafa.17.1_63

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Abstract

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.

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