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Clinical genetics

Showing results (531-540 of 7,173) with videos related to

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Clinical Genetics|March 19, 2010
Large normal and reduced penetrance alleles in Huntington disease: instability in families and frequency at the laboratory, at the clinic and in the populationJ Sequeiros, E M Ramos, J Cerqueira, et al.
Clinical Genetics|March 19, 2010
A homozygous FKRP start codon mutation is associated with Walker-Warburg syndrome, the severe end of the clinical spectrumJ Van Reeuwijk, M J W Olderode-Berends, C Van den Elzen, et al.
Clinical Genetics|March 19, 2010
De novo duplication of MECP2 in a girl with mental retardation and no obvious dysmorphic featuresP Makrythanasis, I Moix, S Gimelli, et al.
Clinical Genetics|July 1, 1989
Albinism and skin cancer in Southern AfricaJ G Kromberg, D Castle, E M Zwane, et al.
Clinical Genetics|July 1, 1989
An aetiological study of isochromosome-X Turner's syndromeA D Carothers, R De Mey, M Daker, et al.
Clinical Genetics|July 1, 1989
De novo Robertsonian D/D type translocations: the Leuven experienceA Kleczkowska, J P Fryns, L Standaert, et al.
Clinical Genetics|August 1, 1989
A genetic epidemiologic investigation of breast cancer in families with bilateral breast cancer. II. Linkage analysisA M Goldstein, R W Haile, M A Spence, et al.
Clinical Genetics|August 24, 2016
Comprehensive review of the duplication 3q syndrome and report of a patient with Currarino syndrome and de novo duplication 3q26.32-q27.2G C Dworschak, C Crétolle, A Hilger, et al.
Clinical Genetics|July 8, 2017
Integrated analysis of SNP, CNV and gene expression data in genetic association studiesR Momtaz, N M Ghanem, N M El-Makky, et al.
Clinical Genetics|July 8, 2017
Mining for mitochondrial mechanisms: Linking known syndromes to mitochondrial functionD M Panneman, J A Smeitink, R J Rodenburg
Pageof 718

Showing results (531-540 of 7,173) with videos related to

Sort By:
Pageof 718
Clinical Genetics|March 19, 2010
Large normal and reduced penetrance alleles in Huntington disease: instability in families and frequency at the laboratory, at the clinic and in the populationJ Sequeiros, E M Ramos, J Cerqueira, et al.
Clinical Genetics|March 19, 2010
A homozygous FKRP start codon mutation is associated with Walker-Warburg syndrome, the severe end of the clinical spectrumJ Van Reeuwijk, M J W Olderode-Berends, C Van den Elzen, et al.
Clinical Genetics|March 19, 2010
De novo duplication of MECP2 in a girl with mental retardation and no obvious dysmorphic featuresP Makrythanasis, I Moix, S Gimelli, et al.
Clinical Genetics|July 1, 1989
Albinism and skin cancer in Southern AfricaJ G Kromberg, D Castle, E M Zwane, et al.
Clinical Genetics|July 1, 1989
An aetiological study of isochromosome-X Turner's syndromeA D Carothers, R De Mey, M Daker, et al.
Clinical Genetics|July 1, 1989
De novo Robertsonian D/D type translocations: the Leuven experienceA Kleczkowska, J P Fryns, L Standaert, et al.
Clinical Genetics|August 1, 1989
A genetic epidemiologic investigation of breast cancer in families with bilateral breast cancer. II. Linkage analysisA M Goldstein, R W Haile, M A Spence, et al.
Clinical Genetics|August 24, 2016
Comprehensive review of the duplication 3q syndrome and report of a patient with Currarino syndrome and de novo duplication 3q26.32-q27.2G C Dworschak, C Crétolle, A Hilger, et al.
Clinical Genetics|July 8, 2017
Integrated analysis of SNP, CNV and gene expression data in genetic association studiesR Momtaz, N M Ghanem, N M El-Makky, et al.
Clinical Genetics|July 8, 2017
Mining for mitochondrial mechanisms: Linking known syndromes to mitochondrial functionD M Panneman, J A Smeitink, R J Rodenburg
Pageof 718