A Chromosome Anomaly New to the “Cri du Chat” Syndrome
Author:
Affiliation:
1. Zoological Institute, Faculty of Science, Hokkaido University
2. Department of Obstetrics and Gynecology, and Department of Pediatrics, School of Medicine, Hokkaido University
Publisher
Japan Academy
Subject
General Medicine
Link
https://www.jstage.jst.go.jp/article/pjab1945/43/10/43_10_986/_pdf
Reference11 articles.
1. M. S. Al-Aish, F, de la Cruz, L. A. Goldsmith, J. Volpe, and J. C. Robinson (1967): New Engl. J. Med., 277, 777-784.
2. D. H. Carr (1967): Am. J. Obst. Gynec., 97, 283-293.
3. D. A. Hungerford (1965): Stain Technol., 40, 333-338.
4. S. L. Inhorn (1966): Advances in Teratology, 2, 37-99.
5. J. Lejeune, J. Lafourcade, R. Berger, J. Vialette, M. Boeswillwald, P. Seringe, and R. Turpin (1963): C. R. Acad. Sc. Paris, 257, 3098-3102.
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1. Cri-du-chat syndrome in a child with a 5/15 translocation and interstitial centromeric heterochromatin;Clinical Genetics;2008-04-23
2. Dermatoglyphics in Cri du Chat syndrome;Clinical Genetics;2008-04-23
3. The cri du chat syndrome;Human Genetics;1978
4. Partial monosomy 22 as the result of an unbalanced translocation 5:22 in a patient with cri-du-chat syndrome;Human Genetics;1976
5. Reciprocal translocations in man. 3:1 Meiotic disjunction resulting in 47- or 45-chromosome offspring.;Journal of Medical Genetics;1975-03-01
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