T Strachan|M Abitbol|D Davidson|J S Beckmann - JoVE Visualize

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Genomics|August 1, 1996

Characterization and chromosomal localization of the gene for human rhodopsin kinaseS C Khani, M Abitbol, S Yamamoto, et al.

Nucleic Acids Research|December 11, 1994

Identification of a novel family of human endogenous retroviruses and characterization of one family member, HERV-K(C4), located in the complement C4 gene clusterM Tassabehji, T Strachan, M Anderson, et al.

Human Molecular Genetics|May 1, 1994

Germline mutations in the neurofibromatosis type 2 tumour suppressor geneD Bourn, S A Carter, S Mason, et al.

Proceedings of the National Academy of Sciences of the United States of America|March 1, 1990

Genesis by meiotic unequal crossover of a de novo deletion that contributes to steroid 21-hydroxylase deficiencyP Sinnott, S Collier, C Costigan, et al.

Human Molecular Genetics|June 1, 1993

A disease-associated germline deletion maps the type 2 neurofibromatosis (NF2) gene between the Ewing sarcoma region and the leukaemia inhibitory factor locusC J Watson, L Gaunt, G Evans, et al.

Journal of Medical Genetics|January 1, 1989

21-hydroxylase deficiency families with HLA identical affected and unaffected sibsP J Sinnott, P A Dyer, D A Price, et al.

The Journal of Laryngology and Otology|September 1, 1995

Variation of expression of the gene for type 2 neurofibromatosis: absence of a gender effect on vestibular schwannomas, but confirmation of a preponderance of meningiomas in femalesD G Evans, V Blair, T Strachan, et al.

Neuroscience|November 27, 2015

Individual differences in impulsive action and dopamine transporter function in rat orbitofrontal cortexJ R Yates, M Darna, J S Beckmann, et al.

Animal Genetics|January 1, 1987

Restriction fragment length polymorphisms in dairy and beef cattle at the growth hormone and prolactin lociE M Hallerman, A Nave, Y Kashi, et al.

Human Molecular Genetics|August 1, 1996

Human Usher 1B/mouse shaker-1: the retinal phenotype discrepancy explained by the presence/absence of myosin VIIA in the photoreceptor cellsA el-Amraoui, I Sahly, S Picaud, et al.

Pageof 96

Showing results (201-210 of 953) with videos related to

Sort By:

Pageof 96

Genomics|August 1, 1996

Characterization and chromosomal localization of the gene for human rhodopsin kinaseS C Khani, M Abitbol, S Yamamoto, et al.

Nucleic Acids Research|December 11, 1994

Identification of a novel family of human endogenous retroviruses and characterization of one family member, HERV-K(C4), located in the complement C4 gene clusterM Tassabehji, T Strachan, M Anderson, et al.

Human Molecular Genetics|May 1, 1994

Germline mutations in the neurofibromatosis type 2 tumour suppressor geneD Bourn, S A Carter, S Mason, et al.

Proceedings of the National Academy of Sciences of the United States of America|March 1, 1990

Genesis by meiotic unequal crossover of a de novo deletion that contributes to steroid 21-hydroxylase deficiencyP Sinnott, S Collier, C Costigan, et al.

Human Molecular Genetics|June 1, 1993

A disease-associated germline deletion maps the type 2 neurofibromatosis (NF2) gene between the Ewing sarcoma region and the leukaemia inhibitory factor locusC J Watson, L Gaunt, G Evans, et al.

Journal of Medical Genetics|January 1, 1989

21-hydroxylase deficiency families with HLA identical affected and unaffected sibsP J Sinnott, P A Dyer, D A Price, et al.

The Journal of Laryngology and Otology|September 1, 1995

Variation of expression of the gene for type 2 neurofibromatosis: absence of a gender effect on vestibular schwannomas, but confirmation of a preponderance of meningiomas in femalesD G Evans, V Blair, T Strachan, et al.

Neuroscience|November 27, 2015

Individual differences in impulsive action and dopamine transporter function in rat orbitofrontal cortexJ R Yates, M Darna, J S Beckmann, et al.

Animal Genetics|January 1, 1987

Restriction fragment length polymorphisms in dairy and beef cattle at the growth hormone and prolactin lociE M Hallerman, A Nave, Y Kashi, et al.

Human Molecular Genetics|August 1, 1996

Human Usher 1B/mouse shaker-1: the retinal phenotype discrepancy explained by the presence/absence of myosin VIIA in the photoreceptor cellsA el-Amraoui, I Sahly, S Picaud, et al.

Pageof 96