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P I Patel

Showing results (61-70 of 85) with videos related to

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American Journal of Human Genetics|May 1, 1996
Molecular analyses of 17p11.2 deletions in 62 Smith-Magenis syndrome patientsR C Juyal, L E Figuera, X Hauge, et al.
American Journal of Medical Genetics|November 20, 1995
Apparent mosaicism for del(17)(p11.2) ruled out by fluorescence in situ hybridization in a Smith-Magenis syndrome patientR C Juyal, B Finucane, L G Shaffer, et al.
Nature|August 2, 1984
Molecular evidence for new mutation at the hprt locus in Lesch-Nyhan patientsT P Yang, P I Patel, A C Chinault, et al.
American Journal of Human Genetics|December 1, 1995
Haploinsufficiency of cytosolic serine hydroxymethyltransferase in the Smith-Magenis syndromeS H Elsea, R C Juyal, S Jiralerspong, et al.
Human Molecular Genetics|April 1, 1995
The gene for a human microfibril-associated glycoprotein is commonly deleted in Smith-Magenis syndrome patientsZ Zhao, C C Lee, S Jiralerspong, et al.
American Journal of Human Genetics|December 1, 1990
Isolation of a marker linked to the Charcot-Marie-Tooth disease type IA gene by differential Alu-PCR of human chromosome 17-retaining hybridsP I Patel, C Garcia, R Montes de Oca-Luna, et al.
Annals of Human Genetics|June 3, 2008
Using population mixtures to optimize the utility of genomic databases: linkage disequilibrium and association study design in IndiaT J Pemberton, M Jakobsson, D F Conrad, et al.
American Journal of Medical Genetics|November 22, 1996
Association study of schizophrenia and the dopamine D3 receptor gene locus in two independent samplesV L Nimgaonkar, A R Sanders, R Ganguli, et al.
Human Molecular Genetics|November 11, 1999
Somatic sequence variation at the Friedreich ataxia locus includes complete contraction of the expanded GAA triplet repeat, significant length variation in serially passaged lymphoblasts and enhanced mutagenesis in the flanking sequenceS I Bidichandani, S M Purandare, E E Taylor, et al.
Cytogenetics and Cell Genetics|January 1, 1997
Definition of the critical interval for Smith-Magenis syndromeS H Elsea, S M Purandare, R A Adell, et al.
Pageof 9

Showing results (61-70 of 85) with videos related to

Sort By:
Pageof 9
American Journal of Human Genetics|May 1, 1996
Molecular analyses of 17p11.2 deletions in 62 Smith-Magenis syndrome patientsR C Juyal, L E Figuera, X Hauge, et al.
American Journal of Medical Genetics|November 20, 1995
Apparent mosaicism for del(17)(p11.2) ruled out by fluorescence in situ hybridization in a Smith-Magenis syndrome patientR C Juyal, B Finucane, L G Shaffer, et al.
Nature|August 2, 1984
Molecular evidence for new mutation at the hprt locus in Lesch-Nyhan patientsT P Yang, P I Patel, A C Chinault, et al.
American Journal of Human Genetics|December 1, 1995
Haploinsufficiency of cytosolic serine hydroxymethyltransferase in the Smith-Magenis syndromeS H Elsea, R C Juyal, S Jiralerspong, et al.
Human Molecular Genetics|April 1, 1995
The gene for a human microfibril-associated glycoprotein is commonly deleted in Smith-Magenis syndrome patientsZ Zhao, C C Lee, S Jiralerspong, et al.
American Journal of Human Genetics|December 1, 1990
Isolation of a marker linked to the Charcot-Marie-Tooth disease type IA gene by differential Alu-PCR of human chromosome 17-retaining hybridsP I Patel, C Garcia, R Montes de Oca-Luna, et al.
Annals of Human Genetics|June 3, 2008
Using population mixtures to optimize the utility of genomic databases: linkage disequilibrium and association study design in IndiaT J Pemberton, M Jakobsson, D F Conrad, et al.
American Journal of Medical Genetics|November 22, 1996
Association study of schizophrenia and the dopamine D3 receptor gene locus in two independent samplesV L Nimgaonkar, A R Sanders, R Ganguli, et al.
Human Molecular Genetics|November 11, 1999
Somatic sequence variation at the Friedreich ataxia locus includes complete contraction of the expanded GAA triplet repeat, significant length variation in serially passaged lymphoblasts and enhanced mutagenesis in the flanking sequenceS I Bidichandani, S M Purandare, E E Taylor, et al.
Cytogenetics and Cell Genetics|January 1, 1997
Definition of the critical interval for Smith-Magenis syndromeS H Elsea, S M Purandare, R A Adell, et al.
Pageof 9