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J M Gardner

Showing results (101-110 of 119) with videos related to

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Human Mutation|February 12, 2000
Mutations of the human P gene associated with Type II oculocutaneous albinism (OCA2). Mutations in brief no. 205. OnlineW S Oetting, J M Gardner, J P Fryer, et al.
Human Gene Therapy|February 1, 1995
In vivo gene delivery and expression of physiological levels of functional human factor VIII in miceS Connelly, T A Smith, G Dhir, et al.
Internal Medicine Journal|December 6, 2003
Novel p53 germline mutation in a patient with Li-Fraumeni syndromeS S Wong, G Lozano, C L Gaff, et al.
American Journal of Human Genetics|September 28, 2001
Mutations in the human orthologue of the mouse underwhite gene (uw) underlie a new form of oculocutaneous albinism, OCA4J M Newton, O Cohen-Barak, N Hagiwara, et al.
Biochemical Genetics|October 1, 1988
Mapping of mouse gamma crystallin genes on chromosome 1L C Skow, M E Donner, S M Huang, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 18, 2005
Superior verbal ability and nonverbal learning disability in a child with a novel 17p12p13.1 deletionD L Steele, A K Chisholm, J D R McGhie, et al.
Nature Genetics|June 1, 1994
African origin of an intragenic deletion of the human P gene in tyrosinase positive oculocutaneous albinismD Durham-Pierre, J M Gardner, Y Nakatsu, et al.
Journal of Biological Regulators and Homeostatic Agents|May 29, 2015
Vascular neoplasm or pseudovascular nevus? Potential pitfalls in diagnosisJ R Kaley, D R Fullen, J M Gardner, et al.
Journal of Medical Genetics|August 3, 2005
Familial scaphocephaly syndrome caused by a novel mutation in the FGFR2 tyrosine kinase domainG McGillivray, R Savarirayan, T C Cox, et al.
Nature|July 29, 1993
A cluster of three GABAA receptor subunit genes is deleted in a neurological mutant of the mouse p locusY Nakatsu, R F Tyndale, T M DeLorey, et al.
Pageof 12

Showing results (101-110 of 119) with videos related to

Sort By:
Pageof 12
Human Mutation|February 12, 2000
Mutations of the human P gene associated with Type II oculocutaneous albinism (OCA2). Mutations in brief no. 205. OnlineW S Oetting, J M Gardner, J P Fryer, et al.
Human Gene Therapy|February 1, 1995
In vivo gene delivery and expression of physiological levels of functional human factor VIII in miceS Connelly, T A Smith, G Dhir, et al.
Internal Medicine Journal|December 6, 2003
Novel p53 germline mutation in a patient with Li-Fraumeni syndromeS S Wong, G Lozano, C L Gaff, et al.
American Journal of Human Genetics|September 28, 2001
Mutations in the human orthologue of the mouse underwhite gene (uw) underlie a new form of oculocutaneous albinism, OCA4J M Newton, O Cohen-Barak, N Hagiwara, et al.
Biochemical Genetics|October 1, 1988
Mapping of mouse gamma crystallin genes on chromosome 1L C Skow, M E Donner, S M Huang, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 18, 2005
Superior verbal ability and nonverbal learning disability in a child with a novel 17p12p13.1 deletionD L Steele, A K Chisholm, J D R McGhie, et al.
Nature Genetics|June 1, 1994
African origin of an intragenic deletion of the human P gene in tyrosinase positive oculocutaneous albinismD Durham-Pierre, J M Gardner, Y Nakatsu, et al.
Journal of Biological Regulators and Homeostatic Agents|May 29, 2015
Vascular neoplasm or pseudovascular nevus? Potential pitfalls in diagnosisJ R Kaley, D R Fullen, J M Gardner, et al.
Journal of Medical Genetics|August 3, 2005
Familial scaphocephaly syndrome caused by a novel mutation in the FGFR2 tyrosine kinase domainG McGillivray, R Savarirayan, T C Cox, et al.
Nature|July 29, 1993
A cluster of three GABAA receptor subunit genes is deleted in a neurological mutant of the mouse p locusY Nakatsu, R F Tyndale, T M DeLorey, et al.
Pageof 12