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Martin Haeusler

Showing results (81-90 of 90) with videos related to

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Birth Defects Research|February 3, 2023
Maternal age and the prevalence of congenital heart defects in Europe, 1995-2015: A register-based studyChrysovalanto Mamasoula, Theophile Bigirumurame, Thomas Chadwick, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|July 29, 2014
Hirschsprung's disease prevalence in Europe: a register based studyKate E Best, Marie-Claude Addor, Larraitz Arriola, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition|November 21, 2014
Epidemiology of congenital diaphragmatic hernia in Europe: a register-based studyMark R McGivern, Kate E Best, Judith Rankin, et al.
American Journal of Medical Genetics. Part A|July 12, 2019
Epidemiology of achondroplasia: A population-based study in EuropeAlessio Coi, Michele Santoro, Ester Garne, et al.
Paediatric and Perinatal Epidemiology|June 16, 2021
Epidemiology of Pierre-Robin sequence in Europe: A population-based EUROCAT studyMichele Santoro, Alessio Coi, Ingeborg Barišić, et al.
Frontiers in Pediatrics|July 12, 2021
Prevention of Neural Tube Defects in Europe: A Public Health FailureJoan K Morris, Marie-Claude Addor, Elisa Ballardini, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|March 8, 2011
Paper 6: EUROCAT member registries: organization and activitiesRuth Greenlees, Amanda Neville, Marie-Claude Addor, et al.
American Journal of Medical Genetics. Part A|December 30, 2022
Amniotic band syndrome and limb body wall complex in Europe 1980-2019Jorieke E H Bergman, Ingeborg Barišić, Marie-Claude Addor, et al.
Pediatric Research|September 10, 2019
Spectrum of congenital anomalies among VACTERL cases: a EUROCAT population-based studyRomy van de Putte, Iris A L M van Rooij, Carlo L M Marcelis, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Structural mapping of GABRB3 variants reveals genotype-phenotype correlationsKatrine M Johannesen, Sumaiya Iqbal, Milena Guazzi, et al.
Pageof 9

Showing results (81-90 of 90) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 90 results.
Birth Defects Research|February 3, 2023
Maternal age and the prevalence of congenital heart defects in Europe, 1995-2015: A register-based studyChrysovalanto Mamasoula, Theophile Bigirumurame, Thomas Chadwick, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|July 29, 2014
Hirschsprung's disease prevalence in Europe: a register based studyKate E Best, Marie-Claude Addor, Larraitz Arriola, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition|November 21, 2014
Epidemiology of congenital diaphragmatic hernia in Europe: a register-based studyMark R McGivern, Kate E Best, Judith Rankin, et al.
American Journal of Medical Genetics. Part A|July 12, 2019
Epidemiology of achondroplasia: A population-based study in EuropeAlessio Coi, Michele Santoro, Ester Garne, et al.
Paediatric and Perinatal Epidemiology|June 16, 2021
Epidemiology of Pierre-Robin sequence in Europe: A population-based EUROCAT studyMichele Santoro, Alessio Coi, Ingeborg Barišić, et al.
Frontiers in Pediatrics|July 12, 2021
Prevention of Neural Tube Defects in Europe: A Public Health FailureJoan K Morris, Marie-Claude Addor, Elisa Ballardini, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|March 8, 2011
Paper 6: EUROCAT member registries: organization and activitiesRuth Greenlees, Amanda Neville, Marie-Claude Addor, et al.
American Journal of Medical Genetics. Part A|December 30, 2022
Amniotic band syndrome and limb body wall complex in Europe 1980-2019Jorieke E H Bergman, Ingeborg Barišić, Marie-Claude Addor, et al.
Pediatric Research|September 10, 2019
Spectrum of congenital anomalies among VACTERL cases: a EUROCAT population-based studyRomy van de Putte, Iris A L M van Rooij, Carlo L M Marcelis, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Structural mapping of GABRB3 variants reveals genotype-phenotype correlationsKatrine M Johannesen, Sumaiya Iqbal, Milena Guazzi, et al.
Pageof 9