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C Hilger

Showing results (61-70 of 93) with videos related to

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Cells|January 22, 2024
<i>PKD1L1</i> Is Involved in Congenital ChylothoraxJonathan B Whitchurch, Sophia Schneider, Alina C Hilger, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|September 25, 2014
Genome-wide mapping of copy number variations in patients with both anorectal malformations and central nervous system abnormalitiesGabriel C Dworschak, Markus Draaken, Alina C Hilger, et al.
European Journal of Human Genetics : EJHG|April 27, 2022
Exome sequencing in individuals with cardiovascular laterality defects identifies potential candidate genesKatinka Breuer, Korbinian M Riedhammer, Nicole Müller, et al.
Allergy|June 28, 2016
Cross-reactivity to fish and chicken meat - a new clinical syndromeA Kuehn, F Codreanu-Morel, C Lehners-Weber, et al.
American Journal of Medical Genetics|July 14, 2000
A European multicenter association study of HTR2A receptor polymorphism in bipolar affective disorderI Massat, D Souery, O Lipp, et al.
Birth Defects Research|February 2, 2018
Exome sequencing in syndromic brain malformations identifies novel mutations in ACTB, and SLC9A6, and suggests BAZ1A as a new candidate geneValerie Weitensteiner, Rong Zhang, Julia Bungenberg, et al.
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|October 23, 2025
Sensing ultrasound localization microscopy for ultrastructural and functional imaging of neonatal kidneysHenriette Grieshaber-Bouyer Mandelbaum, Felix Wachter, Louise Denis, et al.
Human Mutation|August 22, 2015
Targeted Resequencing of 29 Candidate Genes and Mouse Expression Studies Implicate ZIC3 and FOXF1 in Human VATER/VACTERL AssociationAlina C Hilger, Jan Halbritter, Tracie Pennimpede, et al.
Genes|September 28, 2021
Genome-Wide Survey for Microdeletions or -Duplications in 155 Patients with Lower Urinary Tract Obstructions (LUTO)Luca M Schierbaum, Sophia Schneider, Stefan Herms, 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.
Pageof 10

Showing results (61-70 of 93) with videos related to

Sort By:
Pageof 10
Cells|January 22, 2024
<i>PKD1L1</i> Is Involved in Congenital ChylothoraxJonathan B Whitchurch, Sophia Schneider, Alina C Hilger, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|September 25, 2014
Genome-wide mapping of copy number variations in patients with both anorectal malformations and central nervous system abnormalitiesGabriel C Dworschak, Markus Draaken, Alina C Hilger, et al.
European Journal of Human Genetics : EJHG|April 27, 2022
Exome sequencing in individuals with cardiovascular laterality defects identifies potential candidate genesKatinka Breuer, Korbinian M Riedhammer, Nicole Müller, et al.
Allergy|June 28, 2016
Cross-reactivity to fish and chicken meat - a new clinical syndromeA Kuehn, F Codreanu-Morel, C Lehners-Weber, et al.
American Journal of Medical Genetics|July 14, 2000
A European multicenter association study of HTR2A receptor polymorphism in bipolar affective disorderI Massat, D Souery, O Lipp, et al.
Birth Defects Research|February 2, 2018
Exome sequencing in syndromic brain malformations identifies novel mutations in ACTB, and SLC9A6, and suggests BAZ1A as a new candidate geneValerie Weitensteiner, Rong Zhang, Julia Bungenberg, et al.
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|October 23, 2025
Sensing ultrasound localization microscopy for ultrastructural and functional imaging of neonatal kidneysHenriette Grieshaber-Bouyer Mandelbaum, Felix Wachter, Louise Denis, et al.
Human Mutation|August 22, 2015
Targeted Resequencing of 29 Candidate Genes and Mouse Expression Studies Implicate ZIC3 and FOXF1 in Human VATER/VACTERL AssociationAlina C Hilger, Jan Halbritter, Tracie Pennimpede, et al.
Genes|September 28, 2021
Genome-Wide Survey for Microdeletions or -Duplications in 155 Patients with Lower Urinary Tract Obstructions (LUTO)Luca M Schierbaum, Sophia Schneider, Stefan Herms, 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.
Pageof 10