Hydrops fetalis: an unusual prenatal presentation of hereditary congenital lymphedema-Reference-Cited by-同舟云学术

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Hydrops fetalis: an unusual prenatal presentation of hereditary congenital lymphedema

Published:2005 Issue:11 Volume:25 Page:1015-1018
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat. Diagn.

Author:

Daniel-Spiegel Etty,Ghalamkarpour Arash,Spiegel Ronen,Weiner Ehud,Vikkula Miikka,Shalev Eliezer,Shalev Stavit Alon

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Reference21 articles.

1. Nonimmune hydrops fetalis: Clinical experience and factors related to a poor outcome

2. Mapping of Primary Congenital Lymphedema to the 5q35.3 Region

3. Identification of eight novel VEGFR-3 mutations in families with primary congenital lymphoedema

4. Mutations in FOXC2 (MFH-1), a Forkhead Family Transcription Factor, Are Responsible for the Hereditary Lymphedema-Distichiasis Syndrome

5. Hereditary lymphedema: evidence for linkage and genetic heterogeneity

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1. Disorders Affecting Cutaneous Vasculature;Rook's Textbook of Dermatology;2024-03-19

2. Investigation into the genetics of fetal congenital lymphatic anomalies;Prenatal Diagnosis;2023-04-03

3. Two novel variations p.( Ser1275Thr ) and p.( Ser1275Arg ) in FLT4 causing prenatal hereditary lymphedema type 1;Birth Defects Research;2022-12-20

4. A novel stop-gain pathogenic variant in FLT4 and a nonsynonymous pathogenic variant in PTPN11 associated with congenital heart defects;European Journal of Medical Research;2022-12-10

5. Development and physiological functions of the lymphatic system: insights from human genetic studies of primary lymphedema;Physiological Reviews;2021-10-01

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