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Human genetics

Showing results (681-690 of 11,264) with videos related to

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Human Genetics|July 8, 1998
A study of females with deletions of the short arm of the X chromosomeR S James, B Coppin, P Dalton, et al.
Human Genetics|July 8, 1998
A haplotype and linkage disequilibrium analysis of the hereditary hemochromatosis gene regionW Thomas, A Fullan, D B Loeb, et al.
Human Genetics|July 8, 1998
Lack of association between human longevity and genetic polymorphisms in drug-metabolizing enzymes at the NAT2, GSTM1 and CYP2D6 lociM L Muiras, P Verasdonck, F Cottet, et al.
Human Genetics|July 8, 1998
Dopamine beta-hydroxylase: two polymorphisms in linkage disequilibrium at the structural gene DBH associate with biochemical phenotypic variationJ F Cubells, D P van Kammen, M E Kelley, et al.
Human Genetics|July 8, 1998
Three splicing defects, an insertion, and two missense mutations responsible for acute intermittent porphyriaS Mustajoki, H Pihlaja, H Ahola, et al.
Human Genetics|July 8, 1998
High throughput fluorescence-based conformation-sensitive gel electrophoresis (F-CSGE) identifies six unique BRCA2 mutations and an overall low incidence of BRCA2 mutations in high-risk BRCA1-negative breast cancer familiesT Ganguly, R Dhulipala, L Godmilow, et al.
Human Genetics|July 8, 1998
Cystic-fibrosis-like disease unrelated to the cystic fibrosis transmembrane conductance regulatorF Mekus, M Ballmann, I Bronsveld, et al.
Human Genetics|July 8, 1998
The effects of splice site mutations in patients with naevoid basal cell carcinoma syndromeI Smyth, C Wicking, B Wainwright, et al.
Human Genetics|May 14, 2020
Second-tier trio exome sequencing after negative solo clinical exome sequencing: an efficient strategy to increase diagnostic yield and decipher molecular bases in undiagnosed developmental disordersFrederic Tran Mau-Them, Sebastien Moutton, Caroline Racine, et al.
Human Genetics|September 8, 2021
Racial and ethnic disparities in genetic testing for hearing loss: a systematic review and synthesisStephanie L Rouse, Michelle M Florentine, Emily Taketa, et al.
Pageof 1,127

Showing results (681-690 of 11,264) with videos related to

Sort By:
Pageof 1,127
Human Genetics|July 8, 1998
A study of females with deletions of the short arm of the X chromosomeR S James, B Coppin, P Dalton, et al.
Human Genetics|July 8, 1998
A haplotype and linkage disequilibrium analysis of the hereditary hemochromatosis gene regionW Thomas, A Fullan, D B Loeb, et al.
Human Genetics|July 8, 1998
Lack of association between human longevity and genetic polymorphisms in drug-metabolizing enzymes at the NAT2, GSTM1 and CYP2D6 lociM L Muiras, P Verasdonck, F Cottet, et al.
Human Genetics|July 8, 1998
Dopamine beta-hydroxylase: two polymorphisms in linkage disequilibrium at the structural gene DBH associate with biochemical phenotypic variationJ F Cubells, D P van Kammen, M E Kelley, et al.
Human Genetics|July 8, 1998
Three splicing defects, an insertion, and two missense mutations responsible for acute intermittent porphyriaS Mustajoki, H Pihlaja, H Ahola, et al.
Human Genetics|July 8, 1998
High throughput fluorescence-based conformation-sensitive gel electrophoresis (F-CSGE) identifies six unique BRCA2 mutations and an overall low incidence of BRCA2 mutations in high-risk BRCA1-negative breast cancer familiesT Ganguly, R Dhulipala, L Godmilow, et al.
Human Genetics|July 8, 1998
Cystic-fibrosis-like disease unrelated to the cystic fibrosis transmembrane conductance regulatorF Mekus, M Ballmann, I Bronsveld, et al.
Human Genetics|July 8, 1998
The effects of splice site mutations in patients with naevoid basal cell carcinoma syndromeI Smyth, C Wicking, B Wainwright, et al.
Human Genetics|May 14, 2020
Second-tier trio exome sequencing after negative solo clinical exome sequencing: an efficient strategy to increase diagnostic yield and decipher molecular bases in undiagnosed developmental disordersFrederic Tran Mau-Them, Sebastien Moutton, Caroline Racine, et al.
Human Genetics|September 8, 2021
Racial and ethnic disparities in genetic testing for hearing loss: a systematic review and synthesisStephanie L Rouse, Michelle M Florentine, Emily Taketa, et al.
Pageof 1,127