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American Journal of Medical Genetics. Part A
|
August 6, 2021
Exome sequencing of child-parent trios with bladder exstrophy: Findings in 26 children
Georgia Pitsava, Marcia L Feldkamp, Nathan Pankratz, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
October 18, 2011
Bladder exstrophy: an epidemiologic study from the International Clearinghouse for Birth Defects Surveillance and Research, and an overview of the literature
Csaba Siffel, Adolfo Correa, Emmanuelle Amar, et al.
Birth Defects Research
|
August 21, 2025
Comorbidity and Multimorbidity in Adults With Congenital Heart Disease: Findings From a Multi-Site Population-Based Study
Lorenzo D Botto, Matthew R Reeder, George K Lui, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology
|
June 21, 2008
Frequency of holoprosencephaly in the International Clearinghouse Birth Defects Surveillance Systems: searching for population variations
Emanuele Leoncini, Giovanni Baranello, Iêda M Orioli, et al.
American Journal of Perinatology
|
June 1, 2022
A Multicountry Analysis of Prevalence and Mortality among Neonates and Children with Bladder Exstrophy
Vijaya Kancherla, Lucita Tandaki, Manasvi Sundar, et al.
American Journal of Medical Genetics. Part A
|
June 18, 2022
Exome sequencing identifies genetic variants in anophthalmia and microphthalmia
Jingjing Li, Wei Yang, Yuejun Jessie Wang, et al.
Paediatric and Perinatal Epidemiology
|
October 23, 2019
Analysis of Mortality among Neonates and Children with Spina Bifida: An International Registry-Based Study, 2001-2012
Marian K Bakker, Vijaya Kancherla, Mark A Canfield, et al.
Birth Defects Research
|
July 11, 2024
Exome sequencing identifies novel genes underlying primary congenital glaucoma in the National Birth Defects Prevention Study
Elizabeth E Blue, Kristin J Moore, Kari E North, et al.
Birth Defects Research
|
March 11, 2022
Exome sequencing identifies variants in infants with sacral agenesis
Georgia Pitsava, Marcia L Feldkamp, Nathan Pankratz, et al.
Birth Defects Research
|
April 20, 2026
Analysis of Prevalence and Mortality Among Neonates and Children With Intestinal Atresia: A Multinational Study, 1974-2015
Angie Carreño, Maria Paula Aguilera, Lina Ibañez, et al.
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Search research articles
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Showing results (91-100 of 110) with videos related to
Sort By:
Page
of 11
American Journal of Medical Genetics. Part A
|
August 6, 2021
Exome sequencing of child-parent trios with bladder exstrophy: Findings in 26 children
Georgia Pitsava, Marcia L Feldkamp, Nathan Pankratz, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
October 18, 2011
Bladder exstrophy: an epidemiologic study from the International Clearinghouse for Birth Defects Surveillance and Research, and an overview of the literature
Csaba Siffel, Adolfo Correa, Emmanuelle Amar, et al.
Birth Defects Research
|
August 21, 2025
Comorbidity and Multimorbidity in Adults With Congenital Heart Disease: Findings From a Multi-Site Population-Based Study
Lorenzo D Botto, Matthew R Reeder, George K Lui, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology
|
June 21, 2008
Frequency of holoprosencephaly in the International Clearinghouse Birth Defects Surveillance Systems: searching for population variations
Emanuele Leoncini, Giovanni Baranello, Iêda M Orioli, et al.
American Journal of Perinatology
|
June 1, 2022
A Multicountry Analysis of Prevalence and Mortality among Neonates and Children with Bladder Exstrophy
Vijaya Kancherla, Lucita Tandaki, Manasvi Sundar, et al.
American Journal of Medical Genetics. Part A
|
June 18, 2022
Exome sequencing identifies genetic variants in anophthalmia and microphthalmia
Jingjing Li, Wei Yang, Yuejun Jessie Wang, et al.
Paediatric and Perinatal Epidemiology
|
October 23, 2019
Analysis of Mortality among Neonates and Children with Spina Bifida: An International Registry-Based Study, 2001-2012
Marian K Bakker, Vijaya Kancherla, Mark A Canfield, et al.
Birth Defects Research
|
July 11, 2024
Exome sequencing identifies novel genes underlying primary congenital glaucoma in the National Birth Defects Prevention Study
Elizabeth E Blue, Kristin J Moore, Kari E North, et al.
Birth Defects Research
|
March 11, 2022
Exome sequencing identifies variants in infants with sacral agenesis
Georgia Pitsava, Marcia L Feldkamp, Nathan Pankratz, et al.
Birth Defects Research
|
April 20, 2026
Analysis of Prevalence and Mortality Among Neonates and Children With Intestinal Atresia: A Multinational Study, 1974-2015
Angie Carreño, Maria Paula Aguilera, Lina Ibañez, et al.
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of 11