المؤلفون: Siffel, Csaba, Correa, Adolfo, Amar, Emmanuelle, Bakker, Marian K., Bermejo-Sanchez, Eva, Bianca, Sebastiano, Castilla, Eduardo E., Clementi, Maurizio, Cocchi, Guido, Csaky-Szunyogh, Melinda, Feldkamp, Marcia L., Landau, Danielle, Leoncini, Emanuele, Li, Zhu, Lowry, R. Brian, Marengo, Lisa K., Mastroiacovo, Pierpaolo, Morgan, Margery, Mutchinick, Osvaldo M., Pierini, Anna, Rissmann, Anke, Ritvanen, Annukka, Scarano, Gioacchino, Szabova, Elena, Olney, Richard S.

المساهمون: Siffel, C (reprint author), Ctr Dis Control & Prevent, Natl Ctr Birth Defects & Dev Disabil, Metropolitan Atlanta Congenital Defects Program, MailStop E-86,1600 Clifton Rd, Atlanta, GA 30333 USA., Ctr Dis Control & Prevent, Natl Ctr Birth Defects & Dev Disabil, Metropolitan Atlanta Congenital Defects Program, Atlanta, GA 30333 USA., Rhone Alps Registry Birth Defects REMERA, Lyon, France., Univ Groningen, Univ Med Ctr Groningen, Dept Genet, NL-9713 AV Groningen, Netherlands., ISCIII, IIER, Madrid, Spain., ISCIII, CIAC, ECEMC Spanish Collaborat Study Congenital Malform, Madrid, Spain., Ctr Biomed Res Rare Dis, CIBERER, Madrid, Spain., Ctr Consulenza Genet & Teratol Riproduz, Dipartimento Materno Infantile, Lab Citogenet, Catania, Italy., INAGEMP, Brasilia, DF, Brazil., Fundacao Oswaldo Cruz, Inst Oswaldo Cruz, ECLAMC, Rio De Janeiro, Brazil., CEMIC, Buenos Aires, DF, Argentina., Univ Padua, Dept Pediat, Clin Genet Unit, Padua, Italy., Univ Bologna, Dept Pediat, IMER Registry, Bologna, Italy., Natl Ctr Healthcare Audit & Inspect, Dept Hungarian Congenital Abnormal Registry & Sur, Budapest, Hungary., Univ Utah Sch Med, Dept Pediat, Div Med Genet, Salt Lake City, UT USA., Utah Dept Hlth, Utah Birth Defect Network, Salt Lake City, UT 84116 USA., Soroka Univ Med Ctr, Dept Neonatol, Beer Sheva, Israel., Ctr Int Clearinghouse Birth Defects Surveillance, Rome, Italy., Peking Univ Hlth Sci Ctr, Natl Ctr Maternal & Infant Hlth, Beijing, Peoples R China., Alberta Hlth & Wellness, Alberta Congenital Anomalies Surveillance Syst, Calgary, AB, Canada., Texas Dept State Hlth Serv, Birth Defects Epidemiol & Surveillance Branch, Austin, TX USA., Singleton Hosp, CARIS, Swansea SA2 8QA, W Glam, Wales., Inst Nacl Ciencias Med & Nutr Salvador Zubiran, RYVEMCE, Dept Genet, Mexico City, DF, Mexico., CNR Inst Clin Physiol, Pisa, Italy., CNR Tuscany Reg Gabriele Monasterio Fdn, Pisa, Italy., Univ Magdeburg, Fac Med, Malformat Monitoring Ctr Saxony Anhalt, D-39106 Magdeburg, Germany., THL, Natl Inst Hlth & Welf, Helsinki, Finland., Gen Hosp G Rummo Benevento, Dept Med Genet, Birth Defects Campania Registry, Benevento, Italy., Slovak Med Univ, Slovak Teratol Informat Ctr, Bratislava, Slovakia., Ctr Dis Control & Prevent, Natl Ctr Birth Defects & Dev Disabil, Metropolitan Atlanta Congenital Defects Program, MailStop E-86,1600 Clifton Rd, Atlanta, GA 30333 USA.

المصدر: SCI

مصطلحات موضوعية: bladder exstrophy, prevalence, sex ratio, maternal age, TERM-FOLLOW-UP, EPISPADIAS COMPLEX, CLOACAL EXSTROPHY, PRENATAL-DIAGNOSIS, OEIS COMPLEX, CONGENITAL-ABNORMALITIES, ULTRASOUND, ANOMALIES, FAMILIES, RECONSTRUCTION

العلاقة: AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS.2011,157C,(4),321-332.; 896589; http://hdl.handle.net/20.500.11897/237270Test; WOS:000296493300007

الإتاحة: https://doi.org/20.500.11897/237270Test
https://doi.org/10.1002/ajmg.c.30316Test
https://hdl.handle.net/20.500.11897/237270Test

المؤلفون: Feldkamp, Marcia L., Botto, Lorenzo D., Amar, Emmanuelle, Bakker, Marian K., Bermejo-Sanchez, Eva, Bianca, Sebastiano, Canfield, Mark A., Castilla, Eduardo E., Clementi, Maurizio, Csaky-Szunyogh, Melinda, Leoncini, Emanuele, Li, Zhu, Lowry, R. Brian, Mastroiacovo, Pierpaolo, Merlob, Paul, Morgan, Margery, Mutchinick, Osvaldo M., Rissmann, Anke, Ritvanen, Annukka, Siffel, Csaba, Carey, John C.

المساهمون: Feldkamp, ML (reprint author), Univ Utah Sch Med, Div Med Genet, Dept Pediat, 2C 412 SOM,50 N Mario Capecchi Dr, Salt Lake City, UT 84132 USA., Univ Utah Sch Med, Div Med Genet, Dept Pediat, Salt Lake City, UT 84132 USA., Utah Dept Hlth, Utah Birth Defect Network, Salt Lake City, UT 84116 USA., Rhone Alps Registry Birth Defects REMERA, Lyon, France., Univ Groningen, Univ Med Ctr Groningen, Dept Genet, NL-9713 AV Groningen, Netherlands., ISCIII, IIER, Madrid, Spain., ISCIII, ECEMC Spanish Collaborat Study Congenital Malform, CIAC, Madrid, Spain., Ctr Biomed Res Rare Dis, CIBERER, Madrid, Spain., Ctr Consulenza Genet & Teratol Riproduz, Dipartimento Materno Infantile, Lab Citogenet, Catania, Italy., Texas Dept State Hlth Serv, Birth Defects Epidemiol & Surveillance Branch, Austin, TX USA., Fundacao Oswaldo Cruz, Inst Oswaldo Cruz, ECLAMC, Rio De Janeiro, Brazil., CEMIC, Buenos Aires, DF, Argentina., INAGEMP, Brasilia, DF, Brazil., Univ Padua, Dept Pediat, Clin Genet Unit, Padua, Italy., Natl Ctr Healthcare Audit & Inspect, Dept Hungarian Congenital Abnormal Registry & Sur, Budapest, Hungary., Ctr Int Clearinghouse Birth Defects Surveillance, Rome, Italy., Peking Univ Hlth Sci Ctr, Natl Ctr Maternal & Infant Hlth, Beijing, Peoples R China., Alberta Hlth & Wellness, Alberta Congenital Anomalies Surveillance Syst, Calgary, AB, Canada., Rabin Med Ctr, Petah Tiqwa, Israel., Tel Aviv Univ, Tel Aviv, Israel., Singleton Hosp, CARIS, Swansea SA2 8QA, W Glam, Wales., Inst Nacl Ciencias Med & Nutr Salvador Zubiran, RYVEMCE, Dept Genet, Mexico City, DF, Mexico., Univ Magdeburg, Fac Med, Malformat Monitoring Ctr Saxony Anhalt, D-39106 Magdeburg, Germany., THL, Natl Inst Hlth & Welf, Helsinki, Finland., Ctr Dis Control & Prevent, Natl Ctr Birth Defects & Dev Disabil, Metropolitan Atlanta Congenital Defects Program, Atlanta, GA USA., Univ Utah Sch Med, Div Med Genet, Dept Pediat, 2C 412 SOM,50 N Mario Capecchi Dr, Salt Lake City, UT 84132 USA.

المصدر: SCI

مصطلحات موضوعية: cloacal exstrophy, prevalence, birth defects, clinical findings, OEIS complex, ANUS-SPINAL DEFECTS, VESICO-INTESTINAL FISSURE, NEURAL-TUBE DEFECTS, EPISPADIAS COMPLEX, BLADDER EXSTROPHY, IMPERFORATE ANUS, COVERED EXSTROPHY, IDENTICAL-TWINS, CONJOINED TWINS

العلاقة: AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS.2011,157C,(4),333-343.; 896592; http://hdl.handle.net/20.500.11897/237272Test; WOS:000296493300008

الإتاحة: https://doi.org/20.500.11897/237272Test
https://doi.org/10.1002/ajmg.c.30317Test
https://hdl.handle.net/20.500.11897/237272Test