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E C Jenkins

Showing results (91-100 of 146) with videos related to

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American Journal of Medical Genetics|February 1, 1991
SV40-transformed fragile (X) amniocytesE C Jenkins, S E Brooks, S L Stark-Houck, et al.
American Journal of Medical Genetics|August 9, 1996
Reverse mutations in the fragile X syndromeW T Brown, G E Houck, X Ding, et al.
JIMD Reports|April 17, 2013
Substrate Reduction Therapy in Four Patients with Milder CLN1 Mutations and Juvenile-Onset Batten Disease Using Cysteamine BitartrateM Gavin, G Y Wen, J Messing, et al.
The Journal of Biological Chemistry|June 5, 1998
Identification of a candidate human spectrin Src homology 3 domain-binding protein suggests a general mechanism of association of tyrosine kinases with the spectrin-based membrane skeletonD Ziemnicka-Kotula, J Xu, H Gu, et al.
Journal of Cellular Biochemistry|August 1, 1995
Light and electron microscopic immunocytochemical localization of two major proteins in garlic bulbG Y Wen, A Mato, H M Wisniewski, et al.
American Journal of Medical Genetics|April 1, 1992
Fifth international workshop on fragile X and X-linked mental retardationJ L Mandel, R Hagerman, U Froster, et al.
Upsala Journal of Medical Sciences. Supplement|January 1, 1987
Genetics and expression of the fragile X syndromeW T Brown, E C Jenkins, A C Gross, et al.
Clinical Genetics|August 16, 2003
Association of autism severity with a monoamine oxidase A functional polymorphismI L Cohen, X Liu, C Schutz, et al.
Lancet (London, England)|December 5, 1981
Feasibility of fragile X chromosome prenatal diagnosis demonstratedE C Jenkins, W T Brown, C J Duncan, et al.
American Journal of Medical Genetics|April 20, 1999
Accelerated prenatal diagnosis of fragile X syndrome by polymerase chain reaction restriction fragment detectionC Dobkin, X Ding, S Li, et al.
Pageof 15

Showing results (91-100 of 146) with videos related to

Sort By:
Pageof 15
American Journal of Medical Genetics|February 1, 1991
SV40-transformed fragile (X) amniocytesE C Jenkins, S E Brooks, S L Stark-Houck, et al.
American Journal of Medical Genetics|August 9, 1996
Reverse mutations in the fragile X syndromeW T Brown, G E Houck, X Ding, et al.
JIMD Reports|April 17, 2013
Substrate Reduction Therapy in Four Patients with Milder CLN1 Mutations and Juvenile-Onset Batten Disease Using Cysteamine BitartrateM Gavin, G Y Wen, J Messing, et al.
The Journal of Biological Chemistry|June 5, 1998
Identification of a candidate human spectrin Src homology 3 domain-binding protein suggests a general mechanism of association of tyrosine kinases with the spectrin-based membrane skeletonD Ziemnicka-Kotula, J Xu, H Gu, et al.
Journal of Cellular Biochemistry|August 1, 1995
Light and electron microscopic immunocytochemical localization of two major proteins in garlic bulbG Y Wen, A Mato, H M Wisniewski, et al.
American Journal of Medical Genetics|April 1, 1992
Fifth international workshop on fragile X and X-linked mental retardationJ L Mandel, R Hagerman, U Froster, et al.
Upsala Journal of Medical Sciences. Supplement|January 1, 1987
Genetics and expression of the fragile X syndromeW T Brown, E C Jenkins, A C Gross, et al.
Clinical Genetics|August 16, 2003
Association of autism severity with a monoamine oxidase A functional polymorphismI L Cohen, X Liu, C Schutz, et al.
Lancet (London, England)|December 5, 1981
Feasibility of fragile X chromosome prenatal diagnosis demonstratedE C Jenkins, W T Brown, C J Duncan, et al.
American Journal of Medical Genetics|April 20, 1999
Accelerated prenatal diagnosis of fragile X syndrome by polymerase chain reaction restriction fragment detectionC Dobkin, X Ding, S Li, et al.
Pageof 15