A step towards precision medicine in management of severe transient polyhydramnios: MAGED2 variant.

Arthuis, Chloé J; Nizon, Mathilde; Kömhoff, Martin; Beck, Bodo B; Riehmer, Vera; Bihouée, Tiphaine; Bruel, Alexandra; Benbrik, Nadir; Winer, Norbert; Isidor, Bertrand

Arthuis, Chloé J; Nizon, Mathilde; Kömhoff, Martin; Beck, Bodo B; Riehmer, Vera; Bihouée, Tiphaine; Bruel, Alexandra; Benbrik, Nadir; Winer, Norbert; Isidor, Bertrand.

Affiliation

Arthuis CJ; a Service de Gynécologie et Obstétrique, CHU Nantes , Nantes Cedex , France.
Nizon M; b Service de Génétique Médicale, CHU Nantes , Nantes Cedex , France.
Kömhoff M; c University Children's Hospital, Philipps University Marburg , Marburg , Germany.
Beck BB; d Institute of Human Genetics, University of Cologne , Cologne , Germany.
Riehmer V; e Center for Molecular Medicine Cologne (CMMC), University of Cologne , Cologne , Germany.
Bihouée T; d Institute of Human Genetics, University of Cologne , Cologne , Germany.
Bruel A; f Service de Pédiatrie, CHU Nantes , Nantes , France.
Benbrik N; f Service de Pédiatrie, CHU Nantes , Nantes , France.
Winer N; g Service de Cardiologie Pédiatrique, CHU Nantes , Nantes , France.
Isidor B; a Service de Gynécologie et Obstétrique, CHU Nantes , Nantes Cedex , France.

J Obstet Gynaecol ; 39(3): 395-397, 2019 Apr.

Article in En | MEDLINE | ID: mdl-29893154

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bartter Syndrome / Polyhydramnios / Infant, Premature, Diseases Limits: Adult / Female / Humans / Male / Newborn / Pregnancy Language: En Journal: J Obstet Gynaecol Year: 2019 Document type: Article Affiliation country: Francia Country of publication: Reino Unido

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