Publications (876)
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Congenital abnormalities: data needed to establish causes
Congenital abnormalities: data needed to establish causes
Draper E, Rankin J, Tonks A, Boyd P, Wellesley D, Tucker D, Budd J, BINOCAR Management Committee
British Medical Journal, 2009 , 339: b3428
Subjects: Surveillance Methodology -
Congenital anomalies in multiple births after early loss of a conceptus
Congenital anomalies in multiple births after early loss of a conceptus
Pharoah POD, Glinianaia SV, Rankin J
Human Reproduction, 2009 , 24: (3) 726 - 731
Subjects: Other, Prevention & Risk Factors -
Congenital hydronephrosis: prenatal diagnosis and epidemiology in Europe
Congenital hydronephrosis: prenatal diagnosis and epidemiology in Europe
Garne E, Loane M, Wellesley D, Barisic I and EUROCAT Working Group
Journal of Pediatric Urology, 2009 , 5: 47 - 52
Subjects: Prenatal Screening & Diagnosis, Prevalence & Perinatal Mortality
Anomalies: Urinary Anomalies -
Conjoined twins presenting with different sex: description of a second case that truly represents the earliest historical evidence in humans
Conjoined twins presenting with different sex: description of a second case that truly represents the earliest historical evidence in humans
Martinez-Frias M-L
American Journal of Medical Genetics Part A, 2009 , 149A: 1595 - 1596
Subjects: Other, Prevalence & Perinatal Mortality
Anomalies: Chromosomal (other than Down Syndrome) -
Correspondence to the authors: Topiramate in pregnancy: preliminary experience from the UK Epilepsy and Pregnancy Register
Correspondence to the authors: Topiramate in pregnancy: preliminary experience from the UK Epilepsy and Pregnancy Register
Martinez-Frias M-L
Neurology, 2009 , 72: (23) 2054 - 2055
Subjects: Medication During Pregnancy, Prevention & Risk Factors -
Dicentric inverted duplication of entire 4p arm with no apparent deletion and internal placing of the (-TTAGGG-)n sequence: description of the first patient
Dicentric inverted duplication of entire 4p arm with no apparent deletion and internal placing of the (-TTAGGG-)n sequence: description of the first patient
Rodriguez L, Martinez-Fernandez ML, Acena MI, Lopez Mendoza S, Martin Fumero L, Rodriguez de Alba M, Gallego-Merlo J, Martinez-Frias M-L
American Journal of Medical Genetics Part A, 2009 , 149A: 1058 - 1061
Subjects: Genetics and Syndromes -
Epidemiology of acephalus/acardius monozygotic twins: new insights into an epigenetic causal hypothesis
Epidemiology of acephalus/acardius monozygotic twins: new insights into an epigenetic causal hypothesis
Martinez-Frias M-L, ECEMC Working Group
American Journal of Medical Genetics Part A, 2009 , 149A: 640 - 649
Subjects: Other, Prevalence & Perinatal Mortality, Prevention & Risk Factors, Survival & Neuro Development Outcomes
Anomalies: Congenital Heart Anomalies -
EUROCAT Short Report: Congenital Anomalies Diagnosed After Age 1 Year and Their Impact on Prevalence
EUROCAT Short Report: Congenital Anomalies Diagnosed After Age 1 Year and Their Impact on Prevalence
EUROCAT
EUROCAT Central Registry, University of Ulster, 2009
Subjects: Prevalence & Perinatal Mortality, Surveillance Methodology, Survival & Neuro Development Outcomes -
EUROCAT Statistical Monitoring Report 2006
EUROCAT Statistical Monitoring Report 2006
EUROCAT
EUROCAT Central Registry, University of Ulster, 2009
Subjects: Clusters and Trends, Surveillance Methodology -
Further evidence for the involvement of MYH9 in the etiology of non-syndromic cleft lip with or without cleft palate
Further evidence for the involvement of MYH9 in the etiology of non-syndromic cleft lip with or without cleft palate
Birnbaum S, Reutter H, Mende M, de Assis NA, Diaz-Lacava A, Herms S, Scheer M, Lauster C, Braumann B, Schmidt G, Martini M, Hemprich A, Poetzsch S, Knapp M, Nothen MM, Kramer F-J, Mangold E
European Journal of Oral Sciences, 2009 , 117: 200 - 203
Subjects: Genetics and Syndromes
Anomalies: Orofacial clefts