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Human genetics

Showing results (171-180 of 11,257) with videos related to

Pageof 1,126
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Human Genetics|June 15, 2011
The role of the TCF4 gene in the phenotype of individuals with 18q segmental deletionsMinire Hasi, Bridgette Soileau, Courtney Sebold, et al.
Human Genetics|November 1, 1990
Selective advantage of fra (X) heterozygotesF Vogel, W E Crusio, C Kovac, et al.
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: SLC26A4. Disease: Pendred syndromeMohammad Amin Tabatabaiefar, Fatemeh Alasti, Nils Peeters, et al.
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: EXT1. Disease: multiple exostosesWei-De Lin, Fuu-Jer Tsai
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: ACVRL1. Disease: haemorrhagic telangiectasia 2Jay Ellison, Neeraj Kumar
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: APC. Disease: adenomatous polyposis coliT Tuohy, R W Burt
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: HBB. Disease: thalassaemia betaXiaoying Pan
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: RPE65. Disease: Leber congenital amaurosisMamatha Gandra, Anuradha Elamparithi, Srilekha Sundaramurthy, et al.
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: THAP1. Disease: dystonia 6Jianfeng Xiao
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: ABCD1. Disease: X-linked adrenoleukodystrophyCyntia Anabel Amorosi, Helena Treslova, Raquel Dodelson de Kremer, et al.
Pageof 1,126

Showing results (171-180 of 11,257) with videos related to

Sort By:
Pageof 1,126
Human Genetics|June 15, 2011
The role of the TCF4 gene in the phenotype of individuals with 18q segmental deletionsMinire Hasi, Bridgette Soileau, Courtney Sebold, et al.
Human Genetics|November 1, 1990
Selective advantage of fra (X) heterozygotesF Vogel, W E Crusio, C Kovac, et al.
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: SLC26A4. Disease: Pendred syndromeMohammad Amin Tabatabaiefar, Fatemeh Alasti, Nils Peeters, et al.
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: EXT1. Disease: multiple exostosesWei-De Lin, Fuu-Jer Tsai
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: ACVRL1. Disease: haemorrhagic telangiectasia 2Jay Ellison, Neeraj Kumar
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: APC. Disease: adenomatous polyposis coliT Tuohy, R W Burt
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: HBB. Disease: thalassaemia betaXiaoying Pan
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: RPE65. Disease: Leber congenital amaurosisMamatha Gandra, Anuradha Elamparithi, Srilekha Sundaramurthy, et al.
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: THAP1. Disease: dystonia 6Jianfeng Xiao
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: ABCD1. Disease: X-linked adrenoleukodystrophyCyntia Anabel Amorosi, Helena Treslova, Raquel Dodelson de Kremer, et al.
Pageof 1,126