Publications (876)
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EUROCAT Annual Report to WHO 2003
EUROCAT Annual Report to WHO 2003
EUROCAT
EUROCAT Central Registry, University of Ulster, 2003
Subjects: Surveillance Methodology -
EUROCAT Special Report: An Assessment and Analysis of Surveillance Data on Hypospadias in Europe
EUROCAT Special Report: An Assessment and Analysis of Surveillance Data on Hypospadias in Europe
EUROCAT
EUROCAT Central Registry, University of Ulster, 2003
Anomalies: Genital Anomalies -
EUROCAT Special Report: Prevention of Neural Tube Defects by Periconceptional Folic Acid Supplementation in Europe (1st Ed)
EUROCAT Special Report: Prevention of Neural Tube Defects by Periconceptional Folic Acid Supplementation in Europe (1st Ed)
EUROCAT
EUROCAT Central Registry, University of Ulster, 2003
Subjects: Folic Acid
Anomalies: Neural Tube Defects -
EUROCAT Special Report: Using Capture-Recapture Methods to Ascertain Completeness of a Register: Case study and Methodological Considerations
EUROCAT Special Report: Using Capture-Recapture Methods to Ascertain Completeness of a Register: Case study and Methodological Considerations
EUROCAT
EUROCAT Central Registry, University of Ulster, 2003
Subjects: Surveillance Methodology -
First trimester exposure to corticosteroids and oral clefts
First trimester exposure to corticosteroids and oral clefts
Pradat P, Robert-Gnansia E, Di Tanna GL, Rosano A, Lisi A, Mastroiacovo P
Birth Defects Research (Part A), 2003 , 67: 968 - 970
Subjects: Medication During Pregnancy, Prevention & Risk Factors
Anomalies: Orofacial clefts -
Gastrointestinal malformations in Funen County 1980-1993
Gastrointestinal malformations in Funen County 1980-1993
Garne E, Rasmussen L, Husby S
European Journal of Pediatric Surgery, 2003 , 12: (2) 101 - 106
Anomalies: Digestive System Anomalies -
Geographical and ethnic variation of the 677C>T allele of 5,10 methylenetetrahydrofolate reductase (MTHFR): Findings from over 7000 newborns from 16 areas worldwide
Geographical and ethnic variation of the 677C>T allele of 5,10 methylenetetrahydrofolate reductase (MTHFR): Findings from over 7000 newborns from 16 areas worldwide
Wilcken B, Bamforth F, Li Z, Zhu H, Ritvanen A, Redlund M, Stoll C, Alembik Y, Dott B, Czeizel AE, Gelman-Kohan Z, Scarano G, Bianca S, Ettore G, Tenconi R, Bellato S, Scala I, Mutchinick O, Lopez MA, de Walle H, Hofstra R, Joutchenko L, Kavteladze L, Bermejo E, Martinez-Frias M-L, Gallagher MJ, Erickson JD, Vollset S E, Mastroiacovo P, Andria G, Botto L
Journal of Medical Genetics, 2003 , 40: (8) 619 - 625
Subjects: Folic Acid, Genetics and Syndromes -
Incidence of Smith-Lemli-Opitz syndrome in Ontario, Canada. (Letter to the Editor)
Incidence of Smith-Lemli-Opitz syndrome in Ontario, Canada. (Letter to the Editor)
Martinez-Frias M-L, Bermejo E, Rodriguez-Pinilla E
American Journal of Medical Genetics Part A, 2003 , 116: (A) 101
Subjects: Genetics and Syndromes, Prevalence & Perinatal Mortality -
Obesity increases the risk of congenital heart defects in women with gestational diabetes mellitus
Obesity increases the risk of congenital heart defects in women with gestational diabetes mellitus
Frias JP, Martinez-Frias M-L, Frias PA, Frias JL
Diabetologia, 2003 , 46: (A 66) 184
Subjects: Prevention & Risk Factors
Anomalies: Congenital Heart Anomalies -
Prenatal detection of rare chromosomal autosomal abnormalities in Europe
Prenatal detection of rare chromosomal autosomal abnormalities in Europe
Baena N, de Vigan C, Cariati E, Clementi M, Stoll C, Caballin M, Guitart M, EUROSCAN Group
American Journal of Medical Genetics Part A, 2003 , 118a: 319 - 327
Subjects: Prenatal Screening & Diagnosis
Anomalies: Chromosomal (other than Down Syndrome)