Showing results (51-60 of 62) with videos related to
Sort By:
Pageof 7
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 18, 2011
Acardia: epidemiologic findings and literature review from the International Clearinghouse for Birth Defects Surveillance and ResearchLorenzo D Botto, Marcia L Feldkamp, Emmanuelle Amar, et al.American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 18, 2011
Bladder exstrophy: an epidemiologic study from the International Clearinghouse for Birth Defects Surveillance and Research, and an overview of the literatureCsaba Siffel, Adolfo Correa, Emmanuelle Amar, et al.American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 18, 2011
Conjoined twins: a worldwide collaborative epidemiological study of the International Clearinghouse for Birth Defects Surveillance and ResearchOsvaldo M Mutchinick, Leonora Luna-Muñoz, Emmanuelle Amar, et al.Birth Defects Research. Part A, Clinical and Molecular Teratology|June 21, 2008
Frequency of holoprosencephaly in the International Clearinghouse Birth Defects Surveillance Systems: searching for population variationsEmanuele Leoncini, Giovanni Baranello, Iêda M Orioli, et al.The Journal of Pediatrics|March 25, 2014
Clinical features and follow-up in patients with 22q11.2 deletion syndromeCaterina Cancrini, Pamela Puliafito, Maria Cristina Digilio, et al.Birth Defects Research. Part A, Clinical and Molecular Teratology|September 5, 2012
Prevalence of esophageal atresia among 18 international birth defects surveillance programsNatasha Nassar, Emanuele Leoncini, Emmanuelle Amar, et al.Reproductive Toxicology (Elmsford, N.Y.)|June 2, 2005
Preventing neural tube defects in Europe: a missed opportunityAraceli Busby, Lenore Abramsky, Helen Dolk, et al.American Journal of Medical Genetics. Part A|June 26, 2010
How valid are the rates of Down syndrome internationally? Findings from the International Clearinghouse for Birth Defects Surveillance and ResearchEmanuele Leoncini, Lorenzo D Botto, Guido Cocchi, et al.Nature Reviews. Endocrinology|January 30, 2018
Expert consensus document: Clinical and molecular diagnosis, screening and management of Beckwith-Wiedemann syndrome: an international consensus statementFrédéric Brioude, Jennifer M Kalish, Alessandro Mussa, et al.American Journal of Human Genetics|February 4, 2018
Functional Dysregulation of CDC42 Causes Diverse Developmental PhenotypesSimone Martinelli, Oliver H F Krumbach, Francesca Pantaleoni, et al.Pageof 7