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Clinical genetics

Showing results (251-260 of 7,173) with videos related to

Pageof 718
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Clinical Genetics|July 19, 2002
Novel skeletal muscle ryanodine receptor mutation in a large Brazilian family with malignant hyperthermiaS McWilliams, T Nelson, R T Sudo, et al.
Clinical Genetics|July 19, 2002
Supernumerary marker chromosomes derived from chromosome 15: analysis of 32 new casesKatja Eggermann, U A Mau, G Bujdosó, et al.
Clinical Genetics|September 11, 2002
Genotyping of Israeli infertile men with idiopathic oligozoospermiaI Madgar, L Green, M Kent-First, et al.
Clinical Genetics|September 11, 2002
Bronchomalacia associated with pulmonary atresia, ventricular septal defect and major aortopulmonary collateral arteries, and chromosome 22q11.2 deletionH Yamagishi, J Maeda, M Higuchi, et al.
Clinical Genetics|September 11, 2002
Spinal muscular atrophy in black South Africans: concordance with the universal SMN1 genotypeJ M Wilmshurst, L Reynolds, R Van Toorn, et al.
Clinical Genetics|September 11, 2002
Three novel mutations of the PKD1 gene in Korean patients with autosomal dominant polycystic kidney diseaseH-S Eo, J G Lee, C Ahn, et al.
Clinical Genetics|August 16, 2003
Genetic analysis of males from intracytoplasmic sperm injection couplesD G Cruger, I Agerholm, L Byriel, et al.
Clinical Genetics|July 16, 2003
Unique origin and low penetrance of the 946delGAG mutation in Valencian DYT1 familiesJ Carmona, J A Burguera, B Mollà, et al.
Clinical Genetics|November 1, 1975
Ring chromosome 6 in a malformed boyF Salamanca-Gonez, S Nava, S Armendares
Clinical Genetics|September 17, 2003
Genetic landmarks through philately: Georges Marinesco (1863-1938)A E Chudley
Pageof 718

Showing results (251-260 of 7,173) with videos related to

Sort By:
Pageof 718
Clinical Genetics|July 19, 2002
Novel skeletal muscle ryanodine receptor mutation in a large Brazilian family with malignant hyperthermiaS McWilliams, T Nelson, R T Sudo, et al.
Clinical Genetics|July 19, 2002
Supernumerary marker chromosomes derived from chromosome 15: analysis of 32 new casesKatja Eggermann, U A Mau, G Bujdosó, et al.
Clinical Genetics|September 11, 2002
Genotyping of Israeli infertile men with idiopathic oligozoospermiaI Madgar, L Green, M Kent-First, et al.
Clinical Genetics|September 11, 2002
Bronchomalacia associated with pulmonary atresia, ventricular septal defect and major aortopulmonary collateral arteries, and chromosome 22q11.2 deletionH Yamagishi, J Maeda, M Higuchi, et al.
Clinical Genetics|September 11, 2002
Spinal muscular atrophy in black South Africans: concordance with the universal SMN1 genotypeJ M Wilmshurst, L Reynolds, R Van Toorn, et al.
Clinical Genetics|September 11, 2002
Three novel mutations of the PKD1 gene in Korean patients with autosomal dominant polycystic kidney diseaseH-S Eo, J G Lee, C Ahn, et al.
Clinical Genetics|August 16, 2003
Genetic analysis of males from intracytoplasmic sperm injection couplesD G Cruger, I Agerholm, L Byriel, et al.
Clinical Genetics|July 16, 2003
Unique origin and low penetrance of the 946delGAG mutation in Valencian DYT1 familiesJ Carmona, J A Burguera, B Mollà, et al.
Clinical Genetics|November 1, 1975
Ring chromosome 6 in a malformed boyF Salamanca-Gonez, S Nava, S Armendares
Clinical Genetics|September 17, 2003
Genetic landmarks through philately: Georges Marinesco (1863-1938)A E Chudley
Pageof 718