Clinical Manifestations of 22q11.2 Deletion Syndrome-Reference-Cited by-同舟云学术

Clinical Manifestations of 22q11.2 Deletion Syndrome

Published:2022-01 Issue:1 Volume:18 Page:155-164
ISSN:1551-7136
Container-title:Heart Failure Clinics
language:en
Short-container-title:Heart Failure Clinics

Author:

Cirillo Annapaola,Lioncino Michele,Maratea Annachiara,Passariello Annalisa,Fusco Adelaide,Fratta Fiorella,Monda Emanuele,Caiazza Martina,Signore Giovanni,Esposito Augusto,Baban Anwar,Versacci Paolo,Putotto Carolina,Marino Bruno,Pignata Claudio,Cirillo Emilia,Giardino Giuliana,Sarubbi Berardo,Limongelli Giuseppe,Russo Maria Giovanna

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine,General Medicine

Reference65 articles.

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2. Genetic characterisation of 22q11.2 variations and prevalence in patients with congenital heart disease [published correction appears in Arch Dis Child. 2020 May 28;:];Hou;Arch Dis Child,2020

3. Autosomal dominant “Opitz” GBBB syndrome due to a 22q11.2 deletion;McDonald-McGinn;Am J Med Genet,1996

4. Cayler cardiofacial syndrome and del 22q11: part of the CATCH22 phenotype;Giannotti;Am J Med Genet,1994

5. 22q11.2 deletion syndrome;McDonald-McGinn;Nat Rev Dis Primers,2015

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