Three cases with de novo 6q imbalance and variable prenatal phenotype-Reference-Cited by-同舟云学术

Three cases with de novo 6q imbalance and variable prenatal phenotype

Published:2005 Issue:3 Volume:136A Page:254-258
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Grati Francesca R.,Lalatta Faustina,Turolla Licia,Cavallari Ugo,Gentilin Barbara,Rossella Franca,Cetin Irene,Antonazzo Patrizio,Bellotti Maria,Dulcetti Francesca,Baldo Demetrio,Tenconi Romano,Simoni Giuseppe,Miozzo Monica

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference28 articles.

1. Recent Segmental Duplications in the Human Genome

2. Deletion of the SIM1 gene (6q16.2) in a patient with a Prader-Willi-like phenotype

3. Narrowing the candidate region of Albright hereditary osteodystrophy-like syndrome by deletion mapping in a patient with an unbalanced cryptic translocation t(2;6)(q37.3;q26)

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