Hydrops fetalis and pulmonary lymphangiectasia due to FOXC2 mutation: an autosomal dominant hereditary lymphedema syndrome with variable expression

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

Jianming Fang, Susan L. Dagenais, Robert P. Erickson et al. · The American Journal of Human Genetics · 2000 · 613 citations · Full text

Life Sciences, Genetics, Molecular Genetics +10

GJC2 Missense Mutations Cause Human Lymphedema

Robert E. Ferrell, Catherine J. Baty, Mark A. Kimak et al. · The American Journal of Human Genetics · 2010 · 176 citations · Full text

Medicine, Genetics, Molecular Genetics +9

Protein Tyrosine Phosphatase PTPN14 Is a Regulator of Lymphatic Function and Choanal Development in Humans

Audrey C. Au, Paolo A. Hernandez, Ernest Lieber et al. · The American Journal of Human Genetics · 2010 · 96 citations · Full text

Life Sciences, Biochemistry, Cell Biology +12

Nonimmune hydrops fetalis.

Mary E. Norton · PubMed · 1994 · 72 citations

Medicine, Obstetrics, Pathology +15

Hydrops fetalis: an unusual prenatal presentation of hereditary congenital lymphedema

Etty Daniel‐Spiegel, Arash Ghalamkarpour, Ronen Spiegel et al. · Prenatal Diagnosis · 2005 · 68 citations

Medicine, Genetics, Molecular Genetics +15