Unrelated chromosomal anomalies found in patients with suspected 22q11.2 deletion-Reference-Cited by-同舟云学术

Unrelated chromosomal anomalies found in patients with suspected 22q11.2 deletion

Published:2008 Issue:9 Volume:146A Page:1134-1141
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Fernández Luis,Lapunzina Pablo,López Pajares Isidora,Palomares María,Martínez Isabel,Fernández Blanca,Quero José,García-Guereta Luis,García-Alix Alfredo,Burgueros Margarita,Galán-Gómez Enrique,Carbonell-Pérez José María,Pérez-Granero Ángeles,Torres-Juan Laura,Heine-Suñer Damià,Rosell Jordi,Delicado Alicia

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference39 articles.

1. Delineation of a 2.2 Mb microdeletion at 5q35 associated with microcephaly and congenital heart disease

2. Microdeletion and microduplication 22q11.2 screening in 295 patients with clinical features of DiGeorge/Velocardiofacial syndrome

3. Closing time for CATCH22

4. Molecular Definition of 22q11 Deletions in 151 Velo-Cardio-Facial Syndrome Patients

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1. Chromosome 22q11.2 Deletion (DiGeorge Syndrome): Immunologic Features, Diagnosis, and Management;Current Allergy and Asthma Reports;2023-03-10

2. 22q11.2 Deletion Syndrome in Colombian Patients With Syndromic Cleft Lip and/or Palate;The Cleft Palate-Craniofacial Journal;2018-04-13

3. Genomic findings in patients with clinical suspicion of 22q11.2 deletion syndrome;Journal of Applied Genetics;2016-09-14

4. 8p23.1 Interstitial Deletion in a Patient with Congenital Cardiopathy, Neurobehavioral Disorders, and Minor Signs Suggesting 22q11.2 Deletion Syndrome;Journal of Developmental & Behavioral Pediatrics;2015-09

5. 22q11.2 Deletion Syndrome: Laboratory Diagnosis and TBX1 and FGF8 Mutation Screening;Journal of Pediatric Genetics;2015-07-17