M. C. Addor

Prenatal diagnosis of severe structural congenital malformations in Europe

Ester Garne, Maria Loane, Helen Dolk et al. · Ultrasound in Obstetrics and Gynecology · 2004 · 291 citations · Full text

Medicine, Maternal Health, Obstetrics +12

Xq28 duplication including <i><scp>MECP2</scp></i> in six unreported affected females: what can we learn for diagnosis and genetic counselling?

Salima El Chehadeh, Renaud Touraine, Fabienne Prieur et al. · Clinical Genetics · 2016 · 55 citations

Life Sciences, Genetics, Molecular Genetics +17

Anorectal malformations and pregnancy‐related disorders: a registry‐based case–control study in 17 European regions

CHW Wijers, M. C. Addor, Ingeborg Barišić et al. · BJOG An International Journal of Obstetrics & Gynaecology · 2013 · 43 citations · Full text

Medicine, Maternal Health, Obstetrics +17

&lt;i&gt;IRF6&lt;/i&gt; Screening of Syndromic and a priori Non-Syndromic Cleft Lip and Palate Patients: Identification of a New Type of Minor VWS Sign

Laurence Desmyter, Nicole Revençu, Odile Boute et al. · Molecular Syndromology · 2010 · 29 citations · Full text

Dentistry, Genetics, Molecular Genetics +16

Systematic molecular and cytogenetic screening of 100 patients with marfanoid syndromes and intellectual disability

Patrick Callier, Bernard Aral, Nadine Hanna et al. · Clinical Genetics · 2013 · 25 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17