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Charlotte Bendixen

Showing results (1-10 of 10) with videos related to

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Genes|September 28, 2021
The Role of <i>De Novo</i> Variants in Patients with Congenital Diaphragmatic HerniaCharlotte Bendixen, Heiko Reutter
European Journal of Pediatric Surgery : Official Journal of Austrian Association of Pediatric Surgery ... [Et Al] = Zeitschrift Fur Kinderchirurgie|December 15, 2021
Genetic Diagnostic Strategies and Counseling for Families Affected by Congenital Diaphragmatic HerniaCharlotte Bendixen, Erwin Brosens, Wendy Kay Chung
Klinische Padiatrie|October 1, 2019
Prediction of ECMO and Mortality in Neonates with Congenital Diaphragmatic Hernia Using the SNAP-II ScoreFlorian Kipfmueller, Lukas Schroeder, Tamene Melaku, et al.
Zeitschrift Fur Geburtshilfe Und Neonatologie|December 15, 2023
[Characteristics and Outcome of Neonates With Postnatally Diagnosed Congenital Diaphragmatic Hernia]Bartolomeo B L Bo, Lotte Lemloh, Lennart Hale, et al.
BMC Pediatrics|June 15, 2021
Parental risk factors for congenital diaphragmatic hernia - a large German case-control studyFelicitas Schulz, Ekkehart Jenetzky, Nadine Zwink, et al.
Physical Chemistry Chemical Physics : PCCP|April 5, 2016
The structure-function relationship for alumina supported platinum during the formation of ammonia from nitrogen oxide and hydrogen in the presence of oxygenEmma Catherine Adams, Lindsay Richard Merte, Anders Hellman, et al.
Birth Defects Research|April 1, 2022
Re-sequencing of candidate genes FOXF1, HSPA6, HAAO, and KYNU in 522 individuals with VATER/VACTERL, VACTER/VACTERL-like association, and isolated anorectal malformationCorina E Thiem, Jil D Stegmann, Alina C Hilger, et al.
Frontiers in Pediatrics|February 21, 2022
Unraveling the Genetics of Congenital Diaphragmatic Hernia: An Ongoing ChallengeErwin Brosens, Nina C J Peters, Kim S van Weelden, et al.
European Journal of Human Genetics : EJHG|November 2, 2022
Genome-wide identification of disease-causing copy number variations in 450 individuals with anorectal malformationsJulia Fabian, Gabriel C Dworschak, Lea Waffenschmidt, et al.
American Journal of Human Genetics|September 27, 2024
Common variants increase risk for congenital diaphragmatic hernia within the context of de novo variantsLu Qiao, Carrie L Welch, Rebecca Hernan, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Genes|September 28, 2021
The Role of <i>De Novo</i> Variants in Patients with Congenital Diaphragmatic HerniaCharlotte Bendixen, Heiko Reutter
European Journal of Pediatric Surgery : Official Journal of Austrian Association of Pediatric Surgery ... [Et Al] = Zeitschrift Fur Kinderchirurgie|December 15, 2021
Genetic Diagnostic Strategies and Counseling for Families Affected by Congenital Diaphragmatic HerniaCharlotte Bendixen, Erwin Brosens, Wendy Kay Chung
Klinische Padiatrie|October 1, 2019
Prediction of ECMO and Mortality in Neonates with Congenital Diaphragmatic Hernia Using the SNAP-II ScoreFlorian Kipfmueller, Lukas Schroeder, Tamene Melaku, et al.
Zeitschrift Fur Geburtshilfe Und Neonatologie|December 15, 2023
[Characteristics and Outcome of Neonates With Postnatally Diagnosed Congenital Diaphragmatic Hernia]Bartolomeo B L Bo, Lotte Lemloh, Lennart Hale, et al.
BMC Pediatrics|June 15, 2021
Parental risk factors for congenital diaphragmatic hernia - a large German case-control studyFelicitas Schulz, Ekkehart Jenetzky, Nadine Zwink, et al.
Physical Chemistry Chemical Physics : PCCP|April 5, 2016
The structure-function relationship for alumina supported platinum during the formation of ammonia from nitrogen oxide and hydrogen in the presence of oxygenEmma Catherine Adams, Lindsay Richard Merte, Anders Hellman, et al.
Birth Defects Research|April 1, 2022
Re-sequencing of candidate genes FOXF1, HSPA6, HAAO, and KYNU in 522 individuals with VATER/VACTERL, VACTER/VACTERL-like association, and isolated anorectal malformationCorina E Thiem, Jil D Stegmann, Alina C Hilger, et al.
Frontiers in Pediatrics|February 21, 2022
Unraveling the Genetics of Congenital Diaphragmatic Hernia: An Ongoing ChallengeErwin Brosens, Nina C J Peters, Kim S van Weelden, et al.
European Journal of Human Genetics : EJHG|November 2, 2022
Genome-wide identification of disease-causing copy number variations in 450 individuals with anorectal malformationsJulia Fabian, Gabriel C Dworschak, Lea Waffenschmidt, et al.
American Journal of Human Genetics|September 27, 2024
Common variants increase risk for congenital diaphragmatic hernia within the context of de novo variantsLu Qiao, Carrie L Welch, Rebecca Hernan, et al.
Pageof 1