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Prenatal diagnosis
 
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 TitleAuthors / EditorsDate
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 The timing of surgery of antenatally diagnosed choledochal malformations: A descriptive analysis of a 26-year nationwide cohort van den Eijnden, Maria H A; de Kleine, Ruben H; de Blaauw, Ivo; Peeters, Paul M J G; ... Hulscher, Jan B F 2017
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 Phenotypic spectrum and prevalence of INPP5E mutations in Joubert syndrome and related disorders Travaglini, Lorena; Brancati, Francesco; Silhavy, Jennifer; Iannicelli, Miriam; ... Gleeson, Joseph G 2013
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 Congenital fibrinogen disorders De Moerloose, Philippe; Neerman Arbez, Marguerite 2009
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 Normal pregnancy or neoplasia? Rozenholc, Alexandre; Petignat, Patrick 2008
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 Monozygotic twins discordant for trisomy 21 and maternal 21q inheritance: a complex series of events Dahoun, Sophie; Gagos, Sarantis; Gagnebin, Maryline; Gehrig, Corinne; ... Blouin, Jean-Louis 2008
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 Prenatal manifestation in a family affected by nevoid basal cell carcinoma syndrome Le Brun Keris, Yann; Jouk, Pierre-Simon; Saada-Sebag, Géraldine; Roux, Jean-Jacques; ... Lespinasse, James 2008
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 Postnatal management of isolated mild pelvic dilatation detected in antenatal period Merlini, Laura; Parvex, Paloma Maria; Anooshiravani Dumont, Mehrak; Girardin, Eric; Hanquinet, Sylviane 2007
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 Dilatation pyélocalicielle chez le nouveau-né : attitude pratique pour le pédiatre Cachat, F; Ramseyer, P; Meyrat, B J; Frey, P; ... Girardin, Eric 2005
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 Attitudes of future lawyers and psychologists to the use of genetic testing for criminal behavior Elger, Bernice Simone 2005
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 Outcome of children with fetal, neonatal or childhood diagnosis of isolated congenital atrioventricular block. A single institution's experience of 30 years Jaeggi, Edgard; Hamilton, Robert M; Silverman, Earl D; Zamora, Samuel Antonio; Hornberger, Lisa K 2002
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 Pränatale und genetische Aspekte angeborener Herzerkrankungen Fasnacht, M; Jaeggi, Edgard 2001
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 Lessons from the bare lymphocyte syndrome: molecular mechanisms regulating MHC class II expression Waldburger, Jean-Marc; Masternak, Krzysztof; Muhlethaler-Mottet, Annick; Villard, Jean; ... Reith, Walter 2000
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 Prenatal diagnosis of β-thalassaemia in a twin pregnancy using transabdominal CVS sampling Mauron, Alex; Deutsch, S; Darbellay, R; Beck, G; Beris, Photis 1998
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 PCR based mutation screening of the laminin alpha2 chain gene (LAMA2): application to prenatal diagnosis and search for founder effects in congenital muscular dystrophy Guicheney, P; Vignier, N; Zhang, X; He, Y; ... Tryggvason, K 1998