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Marcia L Feldkamp

Showing results (101-110 of 110) with videos related to

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Birth Defects Research|May 28, 2022
Analysis of early neonatal case fatality rate among newborns with congenital hydrocephalus, a 2000-2014 multi-country registry-based studyJuan Antonio Gili, Jorge Santiago López-Camelo, Wendy N Nembhard, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|September 5, 2012
Prevalence of esophageal atresia among 18 international birth defects surveillance programsNatasha Nassar, Emanuele Leoncini, Emmanuelle Amar, et al.
Birth Defects Research|October 17, 2020
A multi-country study of prevalence and early childhood mortality among children with omphaloceleWendy N Nembhard, Jorieke E H Bergman, Maria D Politis, et al.
Annals of Epidemiology|November 30, 2020
Prevalence and mortality in children with congenital diaphragmatic hernia: a multicountry studyMaria D Politis, Eva Bermejo-Sánchez, Mark A Canfield, et al.
Birth Defects Research|November 19, 2022
Prevalence and mortality among children with anorectal malformation: A multi-country analysisVijaya Kancherla, Manasvi Sundar, Lucita Tandaki, et al.
American Journal of Medical Genetics. Part A|June 26, 2010
How valid are the rates of Down syndrome internationally? Findings from the International Clearinghouse for Birth Defects Surveillance and ResearchEmanuele Leoncini, Lorenzo D Botto, Guido Cocchi, et al.
Birth Defects Research|February 27, 2024
Gastroschisis prevalence patterns in 27 surveillance programs from 24 countries, International Clearinghouse for Birth Defects Surveillance and Research, 1980-2017Marcia L Feldkamp, Mark A Canfield, Sergey Krikov, et al.
Birth Defects Research|July 23, 2019
Exome sequencing of family trios from the National Birth Defects Prevention Study: Tapping into a rich resource of genetic and environmental dataMary M Jenkins, Lynn M Almli, Faith Pangilinan, et al.
American Journal of Medical Genetics. Part A|March 21, 2023
Exome-wide assessment of isolated biliary atresia: A report from the National Birth Defects Prevention Study using child-parent trios and a case-control design to identify novel rare variantsPagna Sok, Aniko Sabo, Lynn M Almli, et al.
Genetics in Medicine Open|September 30, 2024
Regulatory elements in <i>SEM1-DLX5-DLX6</i> (7q21.3) locus contribute to genetic control of coronal nonsyndromic craniosynostosis and bone density-related traitsPaola Nicoletti, Samreen Zafer, Lital Matok, et al.
Pageof 11

Showing results (101-110 of 110) with videos related to

Sort By:
Pageof 11
You have reached the last page of results.This site can display upto 110 results.
Birth Defects Research|May 28, 2022
Analysis of early neonatal case fatality rate among newborns with congenital hydrocephalus, a 2000-2014 multi-country registry-based studyJuan Antonio Gili, Jorge Santiago López-Camelo, Wendy N Nembhard, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|September 5, 2012
Prevalence of esophageal atresia among 18 international birth defects surveillance programsNatasha Nassar, Emanuele Leoncini, Emmanuelle Amar, et al.
Birth Defects Research|October 17, 2020
A multi-country study of prevalence and early childhood mortality among children with omphaloceleWendy N Nembhard, Jorieke E H Bergman, Maria D Politis, et al.
Annals of Epidemiology|November 30, 2020
Prevalence and mortality in children with congenital diaphragmatic hernia: a multicountry studyMaria D Politis, Eva Bermejo-Sánchez, Mark A Canfield, et al.
Birth Defects Research|November 19, 2022
Prevalence and mortality among children with anorectal malformation: A multi-country analysisVijaya Kancherla, Manasvi Sundar, Lucita Tandaki, et al.
American Journal of Medical Genetics. Part A|June 26, 2010
How valid are the rates of Down syndrome internationally? Findings from the International Clearinghouse for Birth Defects Surveillance and ResearchEmanuele Leoncini, Lorenzo D Botto, Guido Cocchi, et al.
Birth Defects Research|February 27, 2024
Gastroschisis prevalence patterns in 27 surveillance programs from 24 countries, International Clearinghouse for Birth Defects Surveillance and Research, 1980-2017Marcia L Feldkamp, Mark A Canfield, Sergey Krikov, et al.
Birth Defects Research|July 23, 2019
Exome sequencing of family trios from the National Birth Defects Prevention Study: Tapping into a rich resource of genetic and environmental dataMary M Jenkins, Lynn M Almli, Faith Pangilinan, et al.
American Journal of Medical Genetics. Part A|March 21, 2023
Exome-wide assessment of isolated biliary atresia: A report from the National Birth Defects Prevention Study using child-parent trios and a case-control design to identify novel rare variantsPagna Sok, Aniko Sabo, Lynn M Almli, et al.
Genetics in Medicine Open|September 30, 2024
Regulatory elements in <i>SEM1-DLX5-DLX6</i> (7q21.3) locus contribute to genetic control of coronal nonsyndromic craniosynostosis and bone density-related traitsPaola Nicoletti, Samreen Zafer, Lital Matok, et al.
Pageof 11