Five familial cases with a trisomy 16p syndrome due to translocation

Author:

Leschot N. J.,Nef J. J. De,Geraedts J. P. M.,Becker-Bloemkolk M. J.,Talma A.,Bijlsma J. B.,Verjaal M.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference5 articles.

1. Aetiology of spontaneous abortion. A cytogenetic and epidemiological study of 288 abortuses and their parents;Lauritsen;Acta obstet. gynec. scand.,1976

2. An unusual case of prenatal diagnosis in twin pregnancy;Leschot;Clin. Genet.,1977

3. Trisomy 16p in a liveborn infant and a review of partial and full trisomy 16;Roberts;J. med. Genet.,1978

4. Partial trisomy 16q-;Yunis;Hum. Genet.,1977

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1. An Indian infant with de novo duplication of 16p chromosome: A rare genetic syndrome;Indian Journal of Medical Sciences;2020-12-22

2. Autism Spectrum Disorders;Emery and Rimoin's Principles and Practice of Medical Genetics;2013

3. 16p subtelomeric duplication: a clinically recognizable syndrome;European Journal of Human Genetics;2009-03-18

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