Further delineation of Hennekam syndrome-Reference-Cited by-同舟云学术

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Further delineation of Hennekam syndrome

Published:2003-10 Issue:4 Volume:12 Page:227-232
ISSN:0962-8827
Container-title:Clinical Dysmorphology
language:en
Short-container-title:Clinical Dysmorphology

Author:

Al-Gazali L. I.,Hertecant J.,Ahmed R.,Khan N. A.,Padmanabhan R.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Genetics(clinical),General Medicine,Pathology and Forensic Medicine,Anatomy,Pediatrics, Perinatology, and Child Health

Reference12 articles.

1. Expansion of the phenotype in Hennekam syndrome: A case with new manifestations

2. Craniosynostosis and kidney malformation in a case of Hennekam syndrome

3. Severe lymphedema, intestinal lymphangiectasia, seizures and mild mental retardation: Further case of Hennekam syndrome with a severe phenotype

4. Prox1 is a master control gene in the program specifying lymphatic endothelial cell fate

Cited by 18 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. Surgical resection of a symptomatic intra‐axial lesion in a patient with Hennekam's syndrome: Case report with review of the literature;Neurology and Clinical Neuroscience;2024-03

2. Hennekam Syndrome due to a Novel Homozygous CCBE1 Mutation Presenting as Pediatric-Onset Common Variable Immune Deficiency;Journal of Investigational Allergy and Clinical Immunology;2023-12-11

3. Novel high-risk missense mutations identification in FAT4 gene causing Hennekam syndrome and Van Maldergem syndrome 2 through molecular dynamics simulation;Informatics in Medicine Unlocked;2023

4. A Multiplex Kindred with Hennekam Syndrome due to Homozygosity for a CCBE1 Mutation that does not Prevent Protein Expression;Journal of Clinical Immunology;2015-12-19

5. A Rare Cause of Chylothorax: Hennekam Syndrome;Turkish Thoracic Journal/Türk Toraks Dergisi;2015-01-15

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