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P I Patel

Showing results (31-40 of 85) with videos related to

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American Journal of Medical Genetics|December 11, 1996
Mosaicism for del(17)(p11.2p11.2) underlying the Smith-Magenis syndromeR C Juyal, A Kuwano, I Kondo, et al.
Nature Genetics|December 1, 1992
Charcot-Marie-Tooth type 1A duplication appears to arise from recombination at repeat sequences flanking the 1.5 Mb monomer unitL Pentao, C A Wise, A C Chinault, et al.
American Journal of Medical Genetics|February 5, 1998
Gene for topoisomerase III maps within the Smith-Magenis syndrome critical region: analysis of cell-cycle distribution and radiation sensitivityS H Elsea, E Fritz, R Schoener-Scott, et al.
Nature Genetics|June 1, 1995
Mapping of the congenital generalized hypertrichosis locus to chromosome Xq24-q27.1L E Figuera, M Pandolfo, P W Dunne, et al.
American Journal of Human Genetics|April 1, 1992
Maternal uniparental isodisomy of chromosome 14: association with autosomal recessive rod monochromacyL Pentao, R A Lewis, D H Ledbetter, et al.
European Journal of Human Genetics : EJHG|February 13, 2002
Genomic organisation of the approximately 1.5 Mb Smith-Magenis syndrome critical interval: transcription map, genomic contig, and candidate gene analysisR E Lucas, C N Vlangos, P Das, et al.
American Journal of Medical Genetics|April 29, 1998
Smith-Magenis syndrome resulting from a de novo direct insertion of proximal 17q into 17p11.2J P Park, J B Moeschler, W S Davies, et al.
Journal of Dental Research|September 27, 2000
Clinical, radiographic, and genetic evaluation of a novel form of autosomal-dominant oligodontiaM Goldenberg, P Das, M Messersmith, et al.
Human Molecular Genetics|July 1, 1995
Mapping of genes predisposing to idiopathic generalized epilepsyF Zara, A Bianchi, G Avanzini, et al.
Journal of Medical Genetics|July 25, 1998
Mutation analysis of the nerve specific promoter of the peripheral myelin protein 22 gene in CMT1 disease and HNPPE Nelis, P De Jonghe, E De Vriendt, et al.
Pageof 9

Showing results (31-40 of 85) with videos related to

Sort By:
Pageof 9
American Journal of Medical Genetics|December 11, 1996
Mosaicism for del(17)(p11.2p11.2) underlying the Smith-Magenis syndromeR C Juyal, A Kuwano, I Kondo, et al.
Nature Genetics|December 1, 1992
Charcot-Marie-Tooth type 1A duplication appears to arise from recombination at repeat sequences flanking the 1.5 Mb monomer unitL Pentao, C A Wise, A C Chinault, et al.
American Journal of Medical Genetics|February 5, 1998
Gene for topoisomerase III maps within the Smith-Magenis syndrome critical region: analysis of cell-cycle distribution and radiation sensitivityS H Elsea, E Fritz, R Schoener-Scott, et al.
Nature Genetics|June 1, 1995
Mapping of the congenital generalized hypertrichosis locus to chromosome Xq24-q27.1L E Figuera, M Pandolfo, P W Dunne, et al.
American Journal of Human Genetics|April 1, 1992
Maternal uniparental isodisomy of chromosome 14: association with autosomal recessive rod monochromacyL Pentao, R A Lewis, D H Ledbetter, et al.
European Journal of Human Genetics : EJHG|February 13, 2002
Genomic organisation of the approximately 1.5 Mb Smith-Magenis syndrome critical interval: transcription map, genomic contig, and candidate gene analysisR E Lucas, C N Vlangos, P Das, et al.
American Journal of Medical Genetics|April 29, 1998
Smith-Magenis syndrome resulting from a de novo direct insertion of proximal 17q into 17p11.2J P Park, J B Moeschler, W S Davies, et al.
Journal of Dental Research|September 27, 2000
Clinical, radiographic, and genetic evaluation of a novel form of autosomal-dominant oligodontiaM Goldenberg, P Das, M Messersmith, et al.
Human Molecular Genetics|July 1, 1995
Mapping of genes predisposing to idiopathic generalized epilepsyF Zara, A Bianchi, G Avanzini, et al.
Journal of Medical Genetics|July 25, 1998
Mutation analysis of the nerve specific promoter of the peripheral myelin protein 22 gene in CMT1 disease and HNPPE Nelis, P De Jonghe, E De Vriendt, et al.
Pageof 9