Prenatal diagnosis of Milroy's primary congenital lymphedema
Author:
Publisher
Elsevier BV
Subject
Obstetrics and Gynecology
Reference5 articles.
1. Hereditary lymphedema: evidence for linkage and genetic heterogeneity;Ferrell;Hum Mol Genet,1998
2. Milroy disease. GeneReviews [Internet];Brice,1993
3. Prenatal ultrasonographic diagnosis of atypical Nonne–Milroy lymphedema;Lev-Sagie;Ultrasound Obstet Gynecol,2003
4. Prenatal diagnosis of Milroy's primary congenital lymphedema;Makhoul;Prenat Diagn,2002
5. Prenatal sonographic diagnosis of milroy congenital lymphedema;Wax;J Ultrasound Med,2006
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1. Linfedema primario por enfermedad de Milroy: diagnóstico clínico a partir de un reporte de caso;Acta Pediátrica de México;2024-07-16
2. Current Concepts in the Management of Primary Lymphedema;Medicina;2023-05-06
3. Two novel variations p.( Ser1275Thr ) and p.( Ser1275Arg ) in FLT4 causing prenatal hereditary lymphedema type 1;Birth Defects Research;2022-12-20
4. Prenatal Diagnosis of Milroy's Syndrome;Donald School Journal of Ultrasound in Obstetrics and Gynecology;2022-07-05
5. A family with Milroy disease caused by the FLT4/VEGFR3 gene variant c.2774 T > A;BMC Medical Genomics;2021-06-08
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