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T Strachan

Showing results (51-60 of 138) with videos related to

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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.
Human Molecular Genetics|November 1, 1993
Localisation of a gene for Darier's diseaseR Bashir, C S Munro, S Mason, et al.
American Journal of Human Genetics|July 1, 1994
A mutation in the neurofibromatosis type 2 tumor-suppressor gene, giving rise to widely different clinical phenotypes in two unrelated individualsD Bourn, S A Carter, D G Evans, et al.
Journal of Neurosurgery|December 1, 1994
Diffuse bilateral cerebral astrocytomas with atypical neuroimaging studiesL R Rogers, M A Weinstein, M L Estes, et al.
The EMBO Journal|April 1, 1984
Complete nucleotide sequence of a gene encoding a functional human class I histocompatibility antigen (HLA-CW3)R Sodoyer, M Damotte, T L Delovitch, et al.
Pageof 14

Showing results (51-60 of 138) with videos related to

Sort By:
Pageof 14
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.
Human Molecular Genetics|November 1, 1993
Localisation of a gene for Darier's diseaseR Bashir, C S Munro, S Mason, et al.
American Journal of Human Genetics|July 1, 1994
A mutation in the neurofibromatosis type 2 tumor-suppressor gene, giving rise to widely different clinical phenotypes in two unrelated individualsD Bourn, S A Carter, D G Evans, et al.
Journal of Neurosurgery|December 1, 1994
Diffuse bilateral cerebral astrocytomas with atypical neuroimaging studiesL R Rogers, M A Weinstein, M L Estes, et al.
The EMBO Journal|April 1, 1984
Complete nucleotide sequence of a gene encoding a functional human class I histocompatibility antigen (HLA-CW3)R Sodoyer, M Damotte, T L Delovitch, et al.
Pageof 14