Partial digeorge syndrome with hypertrophied arytenoids in a neonate: Expanding the clinical phenotype-Reference-Cited by-同舟云学术

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Partial digeorge syndrome with hypertrophied arytenoids in a neonate: Expanding the clinical phenotype

Published:2022 Issue:2 Volume:2 Page:110
ISSN:2772-5170
Container-title:Indian Pediatrics Case Reports
language:en
Short-container-title:Indian Pediatr Case Rep

Author:

Madabhushi Siddharth,Saravanamuthu Thirunavukkarasu,Natarajan ChandraKumar,Kumar VaanathiHementha

Publisher

Medknow

Reference10 articles.

1. Prevalence of recurrent pathogenic microdeletions and microduplications in over 9500 pregnancies;Grati;Prenat Diagn,2015

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

3. Velo-cardio-facial syndrome: 30 years of study;Shprintzen;Dev Disabil Res Rev,2008

4. Mitochondrial localization and function of a subset of 22q11 deletion syndrome candidate genes;Maynard;Mol Cell Neurosci,2008

5. Müller W, Peter HH, Kallfelz HC, et al. The DiGeorge sequence. II. Immunologic findings in partial and complete forms of the disorder. Eur J Pediatr 1989;149:96-103.

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