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Wienker

Showing results (111-120 of 282) with videos related to

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Human Heredity|January 1, 1988
Linkage relations of JK, CO, KEL and IGK with each other and with AHCYK Bender, S Bissbort, H Crone, et al.
International Journal of Chronic Obstructive Pulmonary Disease|July 11, 2022
Clinical Impact of Compensatory Hyperinflation of the Nontreated Adjacent Lobe After Bronchoscopic Lung Volume Reduction with ValvesJohannes Wienker, Kaid Darwiche, Julia Wälscher, et al.
American Journal of Human Genetics|September 16, 1999
Investigation of a family with autosomal dominant dilated cardiomyopathy defines a novel locus on chromosome 2q14-q22M Jung, I Poepping, A Perrot, et al.
Hepatology (Baltimore, Md.)|July 13, 2007
Increased gallstone risk in humans conferred by common variant of hepatic ATP-binding cassette transporter for cholesterolFrank Grünhage, Monica Acalovschi, Simona Tirziu, et al.
Human Genetics|September 14, 2007
Gender specific differences in levels of DNA methylation at selected loci from human total blood: a tendency toward higher methylation levels in malesOsman El-Maarri, Tim Becker, Judith Junen, et al.
Human Molecular Genetics|December 1, 1996
Linkage of the gene for the triple A syndrome to chromosome 12q13 near the type II keratin gene clusterA Weber, T F Wienker, M Jung, et al.
Therapeutic Advances in Respiratory Disease|July 4, 2020
Predictive value of Chartis measurement for lung function improvements in bronchoscopic lung volume reductionJohannes Wienker, Rüdiger Karpf-Wissel, Faustina Funke, et al.
Clinical Genetics|March 1, 1985
Norrie's disease: close linkage with genetic markers from the proximal short arm of the X chromosomeA Gal, C Stolzenberger, T Wienker, et al.
Journal of Medical Genetics|January 1, 1989
New mutation to Huntington's diseaseG Wolff, G Deuschl, T F Wienker, et al.
Archives of Iranian Medicine|March 17, 2015
New evidence for the role of calpain 10 in autosomal recessive intellectual disability: identification of two novel nonsense variants by exome sequencing in Iranian familiesMorteza Oladnabi, Luciana Musante, Farzaneh Larti, et al.
Pageof 29

Showing results (111-120 of 282) with videos related to

Sort By:
Pageof 29
Human Heredity|January 1, 1988
Linkage relations of JK, CO, KEL and IGK with each other and with AHCYK Bender, S Bissbort, H Crone, et al.
International Journal of Chronic Obstructive Pulmonary Disease|July 11, 2022
Clinical Impact of Compensatory Hyperinflation of the Nontreated Adjacent Lobe After Bronchoscopic Lung Volume Reduction with ValvesJohannes Wienker, Kaid Darwiche, Julia Wälscher, et al.
American Journal of Human Genetics|September 16, 1999
Investigation of a family with autosomal dominant dilated cardiomyopathy defines a novel locus on chromosome 2q14-q22M Jung, I Poepping, A Perrot, et al.
Hepatology (Baltimore, Md.)|July 13, 2007
Increased gallstone risk in humans conferred by common variant of hepatic ATP-binding cassette transporter for cholesterolFrank Grünhage, Monica Acalovschi, Simona Tirziu, et al.
Human Genetics|September 14, 2007
Gender specific differences in levels of DNA methylation at selected loci from human total blood: a tendency toward higher methylation levels in malesOsman El-Maarri, Tim Becker, Judith Junen, et al.
Human Molecular Genetics|December 1, 1996
Linkage of the gene for the triple A syndrome to chromosome 12q13 near the type II keratin gene clusterA Weber, T F Wienker, M Jung, et al.
Therapeutic Advances in Respiratory Disease|July 4, 2020
Predictive value of Chartis measurement for lung function improvements in bronchoscopic lung volume reductionJohannes Wienker, Rüdiger Karpf-Wissel, Faustina Funke, et al.
Clinical Genetics|March 1, 1985
Norrie's disease: close linkage with genetic markers from the proximal short arm of the X chromosomeA Gal, C Stolzenberger, T Wienker, et al.
Journal of Medical Genetics|January 1, 1989
New mutation to Huntington's diseaseG Wolff, G Deuschl, T F Wienker, et al.
Archives of Iranian Medicine|March 17, 2015
New evidence for the role of calpain 10 in autosomal recessive intellectual disability: identification of two novel nonsense variants by exome sequencing in Iranian familiesMorteza Oladnabi, Luciana Musante, Farzaneh Larti, et al.
Pageof 29