More Clinical Overlap between 22q11.2 Deletion Syndrome and CHARGE Syndrome than Often Anticipated-Reference-Cited by-同舟云学术

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More Clinical Overlap between 22q11.2 Deletion Syndrome and CHARGE Syndrome than Often Anticipated

Published:2013 Issue: Volume: Page:
ISSN:1661-8777
Container-title:Molecular Syndromology
language:en
Short-container-title:Mol Syndromol

Author:

Corsten-Janssen N.,Saitta S.C.,Hoefsloot L.H.,McDonald-McGinn D.M.,Driscoll D.A.,Derks R.,Dickinson K.A.,Kerstjens-Frederikse W.S.,Emanuel B.S.,Zackai E.H.,van Ravenswaaij-Arts C.M.A.

Publisher

S. Karger AG

Subject

Genetics(clinical),Genetics

Cited by 38 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Risk and Resilience Variants in the Retinoic Acid Metabolic and Developmental Pathways Associated with Risk of FASD Outcomes;Biomolecules;2024-05-10

2. CHARGE syndrome, from occurrence to treatment;Human Gene;2023-05

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

4. Neonate with Respiratory Distress, Bilateral Microtia, Hypocalcemia, and Lymphopenia;Pediatrics In Review;2022-05-01

5. Surgical insights and management in patients with the 22q11.2 deletion syndrome;Pediatric Surgery International;2022-04-12

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