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Human genetics

Showing results (101-110 of 11,257) with videos related to

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Human Genetics|February 28, 2003
Prediction of clinical outcome with microarray data: a partial least squares discriminant analysis (PLS-DA) approachMiguel Pérez-Enciso, Michel Tenenhaus
Human Genetics|May 19, 1976
Frequency of chromosomal fluorescence polymorphism in normal persons and in clinical patients with diagnosed chromosome aberrationsE Schwinger, H Wehner
Human Genetics|May 19, 1976
Chromosome measurements on an XXp+ maleK Madan
Human Genetics|May 19, 1976
Cell selection in vivo in normal/aneuploid chromosome abnormalitiesJ Nielsen
Human Genetics|March 5, 2003
A genome-wide scan for primary open-angle glaucoma (POAG): the Barbados Family Study of Open-Angle GlaucomaBarbara Nemesure, Xiaodong Jiao, Qimei He, et al.
Human Genetics|June 13, 2003
Increased variation in mtDNA in patients with familial sensorineural hearing impairmentMervi S Lehtonen, Jukka S Moilanen, Kari Majamaa
Human Genetics|December 1, 1992
Non-radioactive detection of the most common mutations in the cystic fibrosis transmembrane conductance regulator gene by multiplex allele-specific polymerase chain reactionP Fortina, R Conant, G Monokian, et al.
Human Genetics|June 18, 2003
Genome-wide homozygosity mapping localizes a gene for autosomal recessive non-progressive infantile ataxia to 20q11-q13Lisbeth Tranebjaerg, Tanya M Teslovich, MaryPat Jones, et al.
Human Genetics|September 19, 2003
Stratification by CARD15 variant genotype in a genome-wide search for inflammatory bowel disease susceptibility lociSarah H Shaw, Jochen Hampe, Ray White, et al.
Human Genetics|November 22, 2021
Genetic therapies for neurological disordersLaura FitzPatrick, Adrian Bird
Pageof 1,126

Showing results (101-110 of 11,257) with videos related to

Sort By:
Pageof 1,126
Human Genetics|February 28, 2003
Prediction of clinical outcome with microarray data: a partial least squares discriminant analysis (PLS-DA) approachMiguel Pérez-Enciso, Michel Tenenhaus
Human Genetics|May 19, 1976
Frequency of chromosomal fluorescence polymorphism in normal persons and in clinical patients with diagnosed chromosome aberrationsE Schwinger, H Wehner
Human Genetics|May 19, 1976
Chromosome measurements on an XXp+ maleK Madan
Human Genetics|May 19, 1976
Cell selection in vivo in normal/aneuploid chromosome abnormalitiesJ Nielsen
Human Genetics|March 5, 2003
A genome-wide scan for primary open-angle glaucoma (POAG): the Barbados Family Study of Open-Angle GlaucomaBarbara Nemesure, Xiaodong Jiao, Qimei He, et al.
Human Genetics|June 13, 2003
Increased variation in mtDNA in patients with familial sensorineural hearing impairmentMervi S Lehtonen, Jukka S Moilanen, Kari Majamaa
Human Genetics|December 1, 1992
Non-radioactive detection of the most common mutations in the cystic fibrosis transmembrane conductance regulator gene by multiplex allele-specific polymerase chain reactionP Fortina, R Conant, G Monokian, et al.
Human Genetics|June 18, 2003
Genome-wide homozygosity mapping localizes a gene for autosomal recessive non-progressive infantile ataxia to 20q11-q13Lisbeth Tranebjaerg, Tanya M Teslovich, MaryPat Jones, et al.
Human Genetics|September 19, 2003
Stratification by CARD15 variant genotype in a genome-wide search for inflammatory bowel disease susceptibility lociSarah H Shaw, Jochen Hampe, Ray White, et al.
Human Genetics|November 22, 2021
Genetic therapies for neurological disordersLaura FitzPatrick, Adrian Bird
Pageof 1,126