Moebius syndrome and gastroschisis—The second case of a rare association-Reference-Cited by-同舟云学术

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Moebius syndrome and gastroschisis—The second case of a rare association

Published:2023-09-25 Issue:1 Volume:194 Page:111-114
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:American J of Med Genetics Pt A

Author:

Brockmann Knut¹^ORCID,Kaulfuß Silke²

Affiliation:

1. Interdisciplinary Pediatric Center for Children with Developmental Disabilities and Severe Chronic Disorders, Department of Pediatrics and Adolescent Medicine University Medical Center Göttingen Germany

2. Institute of Human Genetics, University Medical Center Göttingen Germany

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.63411

Reference23 articles.

1. Non-coding deletions identify Maenli lncRNA as a limb-specific En1 regulator

2. Comprehensive Developmental Mechanisms in Gastroschisis

3. Subclavian artery supply disruption sequence: Hypothesis of a vascular etiology for Poland, Klippel-Feil, and Möbius anomalies

4. Will the real Moebius syndrome please stand up? A systematic review of the literature and statistical cluster analysis of clinical features

5. Overlap of Moebius and oromandibular limb hypogenesis syndrome with gastroschisis and pulmonary hypoplasia

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