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O Bartsch

Showing results (41-50 of 65) with videos related to

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American Journal of Medical Genetics. Part A|February 27, 2010
Prenatal diagnosis of a recombinant chromosome 7 resulting in trisomy 7q11.22 --> qterM Tchirikov, A Merinsky, M Strohner, et al.
Molecular Syndromology|October 30, 2013
FTO and INSIG2 Genotyping Combined with Metabolic and Anthropometric Phenotyping of Morbidly Obese PatientsE Burgdörfer, M Korenkov, D Jonas, et al.
Molecular Human Reproduction|September 28, 2001
Characterization of relaxin binding in the uterus of the marmoset monkeyA Einspanier, D Müller, J Lubberstedt, et al.
Clinical Genetics|March 3, 2009
Epimutation at human chromosome 14q32.2 in a boy with a upd(14)mat-like clinical phenotypeU Zechner, N Kohlschmidt, G Rittner, et al.
Cytogenetic and Genome Research|August 6, 2003
Microphthalmia with linear skin defects syndrome (MLS): a male with a mosaic paracentric inversion of XpK Kutsche, W Werner, O Bartsch, et al.
Der Anaesthesist|July 23, 2014
[Homozygous and compound heterozygous RYR1 mutations. New findings on prevalence and penetrance of malignant hyperthermia]S Wolak, B Rücker, N Kohlschmidt, et al.
American Journal of Medical Genetics. Part A|October 14, 2004
Three patients with 9p deletions including DMRT1 and DMRT2: a girl with XY complement, bilateral ovotestes, and extreme growth retardation, and two XX females with normal pubertal developmentK Ounap, O Uibo, R Zordania, et al.
Genomics|June 1, 1992
Uniparental isodisomy due to duplication of chromosome 21 occurring in somatic cells monosomic for chromosome 21M B Petersen, O Bartsch, P A Adelsberger, et al.
Human Genetics|July 8, 1998
Deletion mapping by FISH with BACs in patients with partial monosomy 22q13K Schröder, S Schuffenhauer, H Seidel, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 31, 1985
Mass screening for glucose-6-phosphate dehydrogenase deficiency: improved fluorescent spot testE Solem, C Pirzer, M Siege, et al.
Pageof 7

Showing results (41-50 of 65) with videos related to

Sort By:
Pageof 7
American Journal of Medical Genetics. Part A|February 27, 2010
Prenatal diagnosis of a recombinant chromosome 7 resulting in trisomy 7q11.22 --> qterM Tchirikov, A Merinsky, M Strohner, et al.
Molecular Syndromology|October 30, 2013
FTO and INSIG2 Genotyping Combined with Metabolic and Anthropometric Phenotyping of Morbidly Obese PatientsE Burgdörfer, M Korenkov, D Jonas, et al.
Molecular Human Reproduction|September 28, 2001
Characterization of relaxin binding in the uterus of the marmoset monkeyA Einspanier, D Müller, J Lubberstedt, et al.
Clinical Genetics|March 3, 2009
Epimutation at human chromosome 14q32.2 in a boy with a upd(14)mat-like clinical phenotypeU Zechner, N Kohlschmidt, G Rittner, et al.
Cytogenetic and Genome Research|August 6, 2003
Microphthalmia with linear skin defects syndrome (MLS): a male with a mosaic paracentric inversion of XpK Kutsche, W Werner, O Bartsch, et al.
Der Anaesthesist|July 23, 2014
[Homozygous and compound heterozygous RYR1 mutations. New findings on prevalence and penetrance of malignant hyperthermia]S Wolak, B Rücker, N Kohlschmidt, et al.
American Journal of Medical Genetics. Part A|October 14, 2004
Three patients with 9p deletions including DMRT1 and DMRT2: a girl with XY complement, bilateral ovotestes, and extreme growth retardation, and two XX females with normal pubertal developmentK Ounap, O Uibo, R Zordania, et al.
Genomics|June 1, 1992
Uniparental isodisomy due to duplication of chromosome 21 occurring in somatic cells monosomic for chromosome 21M B Petersen, O Bartsch, P A Adelsberger, et al.
Human Genetics|July 8, 1998
Deletion mapping by FISH with BACs in patients with partial monosomy 22q13K Schröder, S Schuffenhauer, H Seidel, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 31, 1985
Mass screening for glucose-6-phosphate dehydrogenase deficiency: improved fluorescent spot testE Solem, C Pirzer, M Siege, et al.
Pageof 7