Cytogenomic characterization of an unexpected 17.6Mb 9p deletion associated to a 14.8Mb 20p duplication in a dysmorphic patient with multiple congenital anomalies presenting a normal G-banding karyotype-Reference-Cited by-同舟云学术

Cytogenomic characterization of an unexpected 17.6Mb 9p deletion associated to a 14.8Mb 20p duplication in a dysmorphic patient with multiple congenital anomalies presenting a normal G-banding karyotype

Published:2012-03 Issue:1 Volume:496 Page:59-62
ISSN:0378-1119
Container-title:Gene
language:en
Short-container-title:Gene

Author:

Meloni Vera de Freitas Ayres,Piazzon Flavia Balbo,Soares Maria de Fátima de Faria,Takeno Sylvia Satomi,Christofolini Denise Maria,Kulikowski Leslie Domenici,Brunoni Decio,Melaragno Maria Isabel

Funder

FAPESP

Publisher

Elsevier BV

Subject

Genetics,General Medicine

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3. Deletion of 20p13 and Duplication of 20p13p12.3 in a Patient with Delayed Speech and Development;Annals of Laboratory Medicine;2018-01-28

4. Combined immunodeficiency in a 3-year-old boy with 16p11.2 and 20p12.2-11.2 chromosomal duplications;American Journal of Medical Genetics Part A;2013-12-05

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