Bladder exstrophy: An epidemiologic study from the International Clearinghouse for Birth Defects Surveillance and Research, and an overview of the literature
Csaba Siffel(Augusta University Health), Richard S. Olney(University of Iowa), Anke Rißmann(Otto-von-Guericke-Universität Magdeburg), Eva Bermejo(Instituto de Salud Carlos III), R. Brian Lowry(Alberta Health Services), Marian K. Bakker(University Medical Center Groningen), Eduardo E. Castilla(Fundação Oswaldo Cruz), Marcia L. Feldkamp(University of Utah), Adolfo Correa(Jackson Memorial Hospital), Lisa K. Marengo(National Center for Environmental Health), Anna Pierini(Istituto di Fisiologia Clinica), Emanuele Leoncini(AbbVie (United States)), Gioacchino Scarano(Azienda Ospedaliera G.Rummo), Melinda Csáky‐Szunyogh(National Public Health and Medical Officer Service), Emmanuelle Amar(Physiopathologie, diagnostic et traitements des maladies musculo-squelettiques), Pierpaolo Mastroiacovo(National Center on Birth Defects and Developmental Disabilities), Annukka Ritvanen, Zhu Li(Zhejiang Chinese Medical University), Elena Szabová(Slovak Medical University), Maurizio Clementi(University of Padua), Danielle Landau(Soroka Medical Center), Margery Morgan(Public Health Wales), Sebastiano Bianca(Institute for Macromolecular Studies), Guido Cocchi(University of Bologna), Osvaldo M. Mutchinick(Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán)
American Journal of Medical Genetics Part C Seminars in Medical Genetics
October 14, 2011
Cited by 119
Related Papers
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes
|Nature Genetics|2018|1.7k
Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa
|Nature Genetics|2019|1.2k
Revised diagnostic criteria for neurofibromatosis type 1 and Legius syndrome: an international consensus recommendation
|Genetics in Medicine|2021|766
Significant Locus and Metabolic Genetic Correlations Revealed in Genome-Wide Association Study of Anorexia Nervosa
|American Journal of Psychiatry|2017|603
Clinical and molecular diagnosis, screening and management of Beckwith–Wiedemann syndrome: an international consensus statement
|Nature Reviews Endocrinology|2018|596