Muenke syndrome: Medical and surgical comorbidities and long‐term management-Reference-Cited by-同舟云学术

Muenke syndrome: Medical and surgical comorbidities and long‐term management

Published:2019-05-20 Issue: Volume: Page:
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Murali Chaya N.¹^ORCID,McDonald‐McGinn Donna M.¹,Wenger Tara Lynn²,McDougall Carey¹,Stroup Bridget M.³^ORCID,Sheppard Sarah E.⁴,Taylor Jesse⁵,Bartlett Scott P.⁵,Bhoj Elizabeth J.¹^ORCID,Zackai Elaine H.¹,Santani Avni⁶

Affiliation:

1. Division of Human GeneticsChildren's Hospital of Philadelphia Philadelphia Pennsylvania

2. Division of Craniofacial MedicineSeattle Children's Hospital Seattle WA

3. Department of Molecular and Human GeneticsBaylor College of Medicine Houston Texas

4. Division of Human Genetics and Center for Applied GenomicsChildren's Hospital of Philadelphia Philadelphia PA

5. Division of Plastic and Reconstructive SurgeryChildren's Hospital of Philadelphia Philadelphia Pennsylvania

6. Department of Pathology and Laboratory MedicineChildren's Hospital of Philadelphia, Perelman School of Medicine, University of Pennsylvania Philadelphia Pennsylvania

Funder

National Institutes of Health

U.S. Public Health Service

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.61199

Reference22 articles.

1. Muenke syndrome with pigmentary disorder and probable hemimegalencephaly: An expansion of the phenotype

2. Epilepsy in Muenke Syndrome: FGFR3-Related Craniosynostosis

3. Identical mutations in three different fibroblast growth factor receptor genes in autosomal dominant craniosynostosis syndromes

4. Muenke syndrome (FGFR3-related craniosynostosis): Expansion of the phenotype and review of the literature

5. Significant phenotypic variability of Muenke syndrome in identical twins

Cited by 3 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. Red blood cell transfusion threshold guidelines in pediatric neurosurgery;Neurosurgical Review;2024-09-06

2. Genetic Testing in Craniofacial Care: Development of Algorithms for Testing Patients with Orofacial Clefting, Branchial Arch Anomalies, and Craniosynostosis;The Cleft Palate Craniofacial Journal;2024-08-18

3. Morbidity Associated With Anterior Versus Posterior Cranial Vault Expansion for Early Treatment of Syndromic Craniosynostosis: A Systematic Review and Meta-Analysis;Journal of Oral and Maxillofacial Surgery;2021-11