Heterozygous deletion of the <i>VEGFC</i> gene in 4q34.3 is associated with Milroy‐like lymphedema: First prenatal case report-Reference-Cited by-同舟云学术

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Heterozygous deletion of the VEGFC gene in 4q34.3 is associated with Milroy‐like lymphedema: First prenatal case report

Published:2022-09-21 Issue:12 Volume:188 Page:3550-3554
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:

Huynh Minh‐Tuan¹²³^ORCID,Degre Sophie⁴,Joly‐Helas Géraldine⁵,Bréon Cathy⁴,Potel Stéphanie⁴,Chambon Pascal⁵,Bouligand Jérôme²³,Layet Valérie¹

Affiliation:

1. Centre Hospitalier du Havre Unité de Génétique Clinique Montivilliers France

2. Laboratoire de Génétique Moléculaire Pharmacogénétique et Hormonologie, Hôpital Bicêtre, APHP Université Paris Saclay Le Kremlin‐Bicêtre France

3. Inserm UMR_S 1185, Faculté de Médecine Paris Saclay Université Paris Saclay Le Kremlin‐Bicêtre France

4. Centre Hospitalier du Havre Service de Gynécologie‐Obstétrique Montivilliers France

5. Centre Hospitalier Universitaire de Rouen Service de Cytogénétique Rouen France

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.62973

Reference10 articles.

1. A novel stop mutation in the vascular endothelial growth factor-C gene (VEGFC) results in Milroy-like disease

2. Genetics of lymphatic anomalies

3. A Simple, Universal, and Cost-Efficient Digital PCR Method for the Targeted Analysis of Copy Number Variations

4. Analysis of the coding regions of VEGFR3 and VEGFC in Milroy disease and other primary lymphoedemas

5. Splice-site mutations in VEGFC cause loss of function and Nonne-Milroy-like primary lymphedema

Cited by 1 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. Prenatal diagnosis and management of Milroy syndrome: a case report;Case Reports in Perinatal Medicine;2023-01-01

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