Etiology and pathogenesis of robin sequence in a large Dutch cohort-Reference-Cited by-同舟云学术

Etiology and pathogenesis of robin sequence in a large Dutch cohort

Published:2015-05-31 Issue:9 Volume:167 Page:1983-1992
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Basart Hanneke¹²,Paes Emma C.³,Maas Saskia M.¹,van den Boogaard Marie-Jose H.⁴,van Hagen Johanna M.⁵,Breugem Corstiaan C.³,Cobben Jan Maarten¹,Don Griot J. Peter W.⁶,Lachmeijer Augusta M. A.⁵,Lichtenbelt Klaske D.⁴,van Nunen Daan P. F.³,van der Horst Chantal M.²,Hennekam Raoul C.¹

Affiliation:

1. Department of Pediatrics; Academic Medical Center; University of Amsterdam; Amsterdam Netherlands

2. Department of Plastic and Reconstructive Surgery; Academic Medical Center; University of Amsterdam; Amsterdam Netherlands

3. Department of Plastic; Reconstructive and Hand Surgery; University Medical Center Utrecht/ Wilhelmina Children's Hospital; Utrecht Netherlands

4. Department of Clinical Genetics; Utrecht Medical Center/Wilhelmina Children's Hospital; Utrecht Netherlands

5. Department of Clinical Genetics; VU Medical Center Amsterdam; Netherlands

6. Department of Plastic; Reconstructive and Hand Surgery; VU Medical Center; Amsterdam Netherlands

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference57 articles.

1. Brainstem dysfunction: A neuroembryological pathogenesis of isolated Pierre Robin sequence;Abadie;Eur J Pediatr,2002

2. The successful use of the nasopharyngeal airway in Pierre Robin sequence: An 11-year experience;Abel;Arch Dis Child,2012

3. Anesthesia for a child with deletion 3q syndrome;Almenrader;Pediatr Anesth,2008

4. Familial microdeletion of 17q24.3 upstream of SOX9 is associated with isolated Pierre Robin sequence due to position effect;Amarillo;Am J Med Genet,2013

5. A syndromic form of Pierre Robin sequence is caused by 5q23 deletions encompassing FBN2 and PHAX;Ansari;Eur J Med Genet,2014

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4. European Guideline Robin Sequence An Initiative From the European Reference Network for Rare Craniofacial Anomalies and Ear, Nose and Throat Disorders (ERN-CRANIO);Journal of Craniofacial Surgery;2023-10-09

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