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Michael Ludwig

Showing results (211-220 of 239) with videos related to

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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.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 13, 2006
Novel OCRL1 mutations in patients with the phenotype of Dent diseaseBoris Utsch, Arend Bökenkamp, Marcus R Benz, et al.
BMC Medical Genetics|May 4, 2016
CNV analysis in 169 patients with bladder exstrophy-epispadias complexCatharina von Lowtzow, Andrea Hofmann, Rong Zhang, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 27, 2015
Investigation of the role of TCF4 rare sequence variants in schizophreniaF Buket Basmanav, Andreas J Forstner, Heide Fier, et al.
Psychiatric Genetics|September 27, 2016
Identification of rare variants in KCTD13 at the schizophrenia risk locus 16p11.2Franziska Degenhardt, Barbara Heinemann, Jana Strohmaier, et al.
Plos Genetics|March 13, 2015
Genome-wide association study and meta-analysis identify ISL1 as genome-wide significant susceptibility gene for bladder exstrophyMarkus Draaken, Michael Knapp, Tracie Pennimpede, et al.
Pediatric Nephrology (Berlin, Germany)|December 7, 2014
Characterization of 28 novel patients expands the mutational and phenotypic spectrum of Lowe syndromeFlorian Recker, Marcin Zaniew, Detlef Böckenhauer, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|May 21, 2014
No major role for periconceptional folic acid use and its interaction with the MTHFR C677T polymorphism in the etiology of congenital anorectal malformationsCharlotte H W Wijers, Ivo de Blaauw, Nadine Zwink, et al.
American Journal of Human Genetics|November 15, 2011
Muscarinic Acetylcholine Receptor M3 Mutation Causes Urinary Bladder Disease and a Prune-Belly-like SyndromeStefanie Weber, Holger Thiele, Sevgi Mir, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|August 19, 2014
Heterozygous FGF8 mutations in patients presenting cryptorchidism and multiple VATER/VACTERL features without limb anomaliesClaudia Zeidler, Joachim Woelfle, Markus Draaken, et al.
Pageof 24

Showing results (211-220 of 239) with videos related to

Sort By:
Pageof 24
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.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 13, 2006
Novel OCRL1 mutations in patients with the phenotype of Dent diseaseBoris Utsch, Arend Bökenkamp, Marcus R Benz, et al.
BMC Medical Genetics|May 4, 2016
CNV analysis in 169 patients with bladder exstrophy-epispadias complexCatharina von Lowtzow, Andrea Hofmann, Rong Zhang, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 27, 2015
Investigation of the role of TCF4 rare sequence variants in schizophreniaF Buket Basmanav, Andreas J Forstner, Heide Fier, et al.
Psychiatric Genetics|September 27, 2016
Identification of rare variants in KCTD13 at the schizophrenia risk locus 16p11.2Franziska Degenhardt, Barbara Heinemann, Jana Strohmaier, et al.
Plos Genetics|March 13, 2015
Genome-wide association study and meta-analysis identify ISL1 as genome-wide significant susceptibility gene for bladder exstrophyMarkus Draaken, Michael Knapp, Tracie Pennimpede, et al.
Pediatric Nephrology (Berlin, Germany)|December 7, 2014
Characterization of 28 novel patients expands the mutational and phenotypic spectrum of Lowe syndromeFlorian Recker, Marcin Zaniew, Detlef Böckenhauer, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|May 21, 2014
No major role for periconceptional folic acid use and its interaction with the MTHFR C677T polymorphism in the etiology of congenital anorectal malformationsCharlotte H W Wijers, Ivo de Blaauw, Nadine Zwink, et al.
American Journal of Human Genetics|November 15, 2011
Muscarinic Acetylcholine Receptor M3 Mutation Causes Urinary Bladder Disease and a Prune-Belly-like SyndromeStefanie Weber, Holger Thiele, Sevgi Mir, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|August 19, 2014
Heterozygous FGF8 mutations in patients presenting cryptorchidism and multiple VATER/VACTERL features without limb anomaliesClaudia Zeidler, Joachim Woelfle, Markus Draaken, et al.
Pageof 24