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Heiko Reutter

Showing results (191-200 of 209) with videos related to

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Brain : a Journal of Neurology|April 16, 2020
Novel congenital disorder of O-linked glycosylation caused by GALNT2 loss of functionMonica Zilmer, Andrew C Edmondson, Sumeet A Khetarpal, et al.
Nature Genetics|March 10, 2009
Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24Stefanie Birnbaum, Kerstin U Ludwig, Heiko Reutter, et al.
Human Molecular Genetics|May 24, 2014
Genome-wide association study and mouse expression data identify a highly conserved 32 kb intergenic region between WNT3 and WNT9b as possible susceptibility locus for isolated classic exstrophy of the bladderHeiko Reutter, Markus Draaken, Tracie Pennimpede, et al.
American Journal of Human Genetics|November 12, 2019
CAKUT and Autonomic Dysfunction Caused by Acetylcholine Receptor MutationsNina Mann, Franziska Kause, Erik K Henze, et al.
Nature Genetics|August 7, 2012
Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk lociKerstin U Ludwig, Elisabeth Mangold, Stefan Herms, et al.
Nature Genetics|December 22, 2009
Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palateElisabeth Mangold, Kerstin U Ludwig, Stefanie Birnbaum, et al.
Plos One|May 29, 2019
Exome chip association study excluded the involvement of rare coding variants with large effect sizes in the etiology of anorectal malformationsRomy van de Putte, Charlotte H W Wijers, Heiko Reutter, et al.
Clinical Genetics|May 6, 2021
ANKRD11 variants: KBG syndrome and beyondIlaria Parenti, Mark B Mallozzi, Irina Hüning, et al.
Scientific Reports|February 9, 2017
ISL1 is a major susceptibility gene for classic bladder exstrophy and a regulator of urinary tract developmentRong Zhang, Michael Knapp, Kentaro Suzuki, et al.
Genes|August 29, 2024
A Genotype/Phenotype Study of <i>KDM5B</i>-Associated Disorders Suggests a Pathogenic Effect of Dominantly Inherited Missense VariantsMaria Carla Borroto, Coralie Michaud, Chloé Hudon, et al.
Pageof 21

Showing results (191-200 of 209) with videos related to

Sort By:
Pageof 21
Brain : a Journal of Neurology|April 16, 2020
Novel congenital disorder of O-linked glycosylation caused by GALNT2 loss of functionMonica Zilmer, Andrew C Edmondson, Sumeet A Khetarpal, et al.
Nature Genetics|March 10, 2009
Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24Stefanie Birnbaum, Kerstin U Ludwig, Heiko Reutter, et al.
Human Molecular Genetics|May 24, 2014
Genome-wide association study and mouse expression data identify a highly conserved 32 kb intergenic region between WNT3 and WNT9b as possible susceptibility locus for isolated classic exstrophy of the bladderHeiko Reutter, Markus Draaken, Tracie Pennimpede, et al.
American Journal of Human Genetics|November 12, 2019
CAKUT and Autonomic Dysfunction Caused by Acetylcholine Receptor MutationsNina Mann, Franziska Kause, Erik K Henze, et al.
Nature Genetics|August 7, 2012
Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk lociKerstin U Ludwig, Elisabeth Mangold, Stefan Herms, et al.
Nature Genetics|December 22, 2009
Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palateElisabeth Mangold, Kerstin U Ludwig, Stefanie Birnbaum, et al.
Plos One|May 29, 2019
Exome chip association study excluded the involvement of rare coding variants with large effect sizes in the etiology of anorectal malformationsRomy van de Putte, Charlotte H W Wijers, Heiko Reutter, et al.
Clinical Genetics|May 6, 2021
ANKRD11 variants: KBG syndrome and beyondIlaria Parenti, Mark B Mallozzi, Irina Hüning, et al.
Scientific Reports|February 9, 2017
ISL1 is a major susceptibility gene for classic bladder exstrophy and a regulator of urinary tract developmentRong Zhang, Michael Knapp, Kentaro Suzuki, et al.
Genes|August 29, 2024
A Genotype/Phenotype Study of <i>KDM5B</i>-Associated Disorders Suggests a Pathogenic Effect of Dominantly Inherited Missense VariantsMaria Carla Borroto, Coralie Michaud, Chloé Hudon, et al.
Pageof 21