Prenatal molecular testing for Beckwith–Wiedemann and Silver–Russell syndromes: a challenge for molecular analysis and genetic counseling-Reference-Cited by-同舟云学术

Prenatal molecular testing for Beckwith–Wiedemann and Silver–Russell syndromes: a challenge for molecular analysis and genetic counseling

Published:2015-10-28 Issue:6 Volume:24 Page:784-793
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Eggermann Thomas,Brioude Frédéric,Russo Silvia,Lombardi Maria P,Bliek Jet,Maher Eamonn R,Larizza Lidia,Prawitt Dirk,Netchine Irène,Gonzales Marie,Grønskov Karen,Tümer Zeynep,Monk David,Mannens Marcel,Chrzanowska Krystyna,Walasek Malgorzata K,Begemann Matthias^ORCID,Soellner Lukas,Eggermann Katja,Tenorio Jair,Nevado Julián,Moore Gudrun E,Mackay Deborah JG,Temple Karen,Gillessen-Kaesbach Gabriele,Ogata Tsutomu,Weksberg Rosanna,Algar Elizabeth,Lapunzina Pablo

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

https://www.nature.com/articles/ejhg2015224.pdf

Reference44 articles.

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3. Eggermann T, Netchine I, Temple IK et al: Congenital imprinting disorders: EUCID.net - a network to decipher their aetiology and to improve the diagnostic and clinical care. Clin Epigenetics 2015; 7: 23.

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