Search research articles
Contact Us
Filters
Showing results (81-90 of 209) with videos related to
Page
of 21
Sort By:
Archives of Gynecology and Obstetrics
|
May 23, 2019
Isolated bladder exstrophy in prenatal diagnosis
Michael R Mallmann, Birte Mack-Detlefsen, Heiko Reutter, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies
|
December 19, 2015
Whole-Exome Sequencing in Nine Monozygotic Discordant Twins
Rong Zhang, Holger Thiele, Peter Bartmann, et al.
Asia Pacific Journal of Clinical Nutrition
|
December 10, 2017
Low maternal folate concentrations and maternal MTHFR C677T polymorphism are associated with an increased risk for neural tube defects in offspring: a case-control study among Pakistani case and control mothers
Nuzhat Nauman, Samina Jalali, Sajjad Shami, et al.
European Journal of Medical Genetics
|
September 21, 2010
De novo microduplication at 22q11.21 in a patient with VACTERL association
Charlotte Schramm, Markus Draaken, Enrika Bartels, et al.
European Journal of Medical Genetics
|
November 3, 2011
Primary pulmonary hypertension, congenital heart defect, central nervous system malformations, hypo- and aplastic toes: another case of Yunis-Varón syndrome or report of a new entity
Heiko Reutter, Soyhan Bagci, Andreas Müller, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology
|
September 10, 2014
Bladder exstrophy-epispadias complex and triple-X syndrome: incidental finding or causality?
Paul Ramaekers, Bart Loeys, Catharina von Lowtzow, et al.
Journal of Pediatric Urology
|
May 20, 2015
Sexual function in adult patients with classic bladder exstrophy: A multicenter study
Weon Park, Nadine Zwink, Wolfgang H Rösch, et al.
Pediatric Surgery International
|
March 17, 2012
Familial occurrence of the VATER/VACTERL association
Alina Hilger, Charlotte Schramm, Markus Draaken, et al.
BMC Pediatrics
|
June 15, 2021
Parental risk factors for congenital diaphragmatic hernia - a large German case-control study
Felicitas Schulz, Ekkehart Jenetzky, Nadine Zwink, et al.
Pediatric Nephrology (Berlin, Germany)
|
February 4, 2025
Oral health status in children with chronic kidney disease, kidney transplantation, and nephrotic syndrome: a cross-sectional study
Anna Beyer, Fabian Ebach, Heiko Reutter, et al.
Page
of 21
Search research articles
Search
Showing results (81-90 of 209) with videos related to
Sort By:
Page
of 21
Archives of Gynecology and Obstetrics
|
May 23, 2019
Isolated bladder exstrophy in prenatal diagnosis
Michael R Mallmann, Birte Mack-Detlefsen, Heiko Reutter, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies
|
December 19, 2015
Whole-Exome Sequencing in Nine Monozygotic Discordant Twins
Rong Zhang, Holger Thiele, Peter Bartmann, et al.
Asia Pacific Journal of Clinical Nutrition
|
December 10, 2017
Low maternal folate concentrations and maternal MTHFR C677T polymorphism are associated with an increased risk for neural tube defects in offspring: a case-control study among Pakistani case and control mothers
Nuzhat Nauman, Samina Jalali, Sajjad Shami, et al.
European Journal of Medical Genetics
|
September 21, 2010
De novo microduplication at 22q11.21 in a patient with VACTERL association
Charlotte Schramm, Markus Draaken, Enrika Bartels, et al.
European Journal of Medical Genetics
|
November 3, 2011
Primary pulmonary hypertension, congenital heart defect, central nervous system malformations, hypo- and aplastic toes: another case of Yunis-Varón syndrome or report of a new entity
Heiko Reutter, Soyhan Bagci, Andreas Müller, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology
|
September 10, 2014
Bladder exstrophy-epispadias complex and triple-X syndrome: incidental finding or causality?
Paul Ramaekers, Bart Loeys, Catharina von Lowtzow, et al.
Journal of Pediatric Urology
|
May 20, 2015
Sexual function in adult patients with classic bladder exstrophy: A multicenter study
Weon Park, Nadine Zwink, Wolfgang H Rösch, et al.
Pediatric Surgery International
|
March 17, 2012
Familial occurrence of the VATER/VACTERL association
Alina Hilger, Charlotte Schramm, Markus Draaken, et al.
BMC Pediatrics
|
June 15, 2021
Parental risk factors for congenital diaphragmatic hernia - a large German case-control study
Felicitas Schulz, Ekkehart Jenetzky, Nadine Zwink, et al.
Pediatric Nephrology (Berlin, Germany)
|
February 4, 2025
Oral health status in children with chronic kidney disease, kidney transplantation, and nephrotic syndrome: a cross-sectional study
Anna Beyer, Fabian Ebach, Heiko Reutter, et al.
Page
of 21