Duplication of chromosome region (16)(p11.2 ? p12.1) in a mother and daughter with mild mental retardation-Reference-Cited by-同舟云学术

Duplication of chromosome region (16)(p11.2 ? p12.1) in a mother and daughter with mild mental retardation

Published:2002-04-19 Issue:2 Volume:109 Page:149-153
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Engelen J.J.M.,de Die-Smulders C.E.M.,Dirckx R.,Verhoeven W.M.A.,Tuinier S.,Curfs L.M.G.,Hamers A.J.H.

Publisher

Wiley

Subject

Genetics (clinical)

Reference24 articles.

1. Amplification of a pseudogene cassette underlies euchromatic variation of 16p at the cytogenetic level

2. 1978. Chromosome anomalies associated with fetal malformations. In: editor. Toward the prevention of fetal malformation. Edinburgh: Edinburgh University Press. p 49-65.

3. Duplication of euchromatin without phenotypic effects: A variant of chromosome 16

4. Chromosome anomalies as a cause of spontaneous abortion

5. De novo trisomy 16p

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2. Triplication of 16p12.1p12.3 associated with developmental and growth delay and distinctive facial features;American Journal of Medical Genetics Part A;2015-12-08

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