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C A Wise

Showing results (11-20 of 25) with videos related to

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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.
Arthritis and Rheumatism|October 3, 2000
Localization of a gene for familial recurrent arthritisC A Wise, L B Bennett, V Pascual, et al.
Spine|September 14, 2000
Localization of susceptibility to familial idiopathic scoliosisC A Wise, R Barnes, J Gillum, et al.
Journal of Occupational Rehabilitation|November 19, 2013
Reliability of a digital electroneurometer for the determination of motor latency of the median nerveT M Cook, J C Rosecrance, S J Brokman, et al.
Journal of Medical Genetics|April 16, 2002
DTDST mutations are not a frequent cause of idiopathic talipes equinovarus (club foot)L Bonafé, S H Blanton, A Scott, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|March 1, 1992
Subcutaneous tocolytic infusion therapy for patients at very high risk for preterm birthJ R Allbert, C A Wise, C H Lou, et al.
American Journal of Human Genetics|October 1, 1993
Molecular analyses of unrelated Charcot-Marie-Tooth (CMT) disease patients suggest a high frequency of the CMTIA duplicationC A Wise, C A Garcia, S N Davis, et al.
Progress in Clinical and Biological Research|January 1, 1993
Gene dosage as a mechanism for a common autosomal dominant peripheral neuropathy: Charcot-Marie-Tooth disease type 1AB B Roa, C A Garcia, C A Wise, et al.
Methods in Enzymology|January 1, 1996
Genetic and biochemical approaches for analysis of mitochondrial RNase P from Saccharomyces cerevisiaeK R Groom, Y L Dang, G J Gao, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1997
TCOF1 gene encodes a putative nucleolar phosphoprotein that exhibits mutations in Treacher Collins Syndrome throughout its coding regionC A Wise, L C Chiang, W A Paznekas, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
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.
Arthritis and Rheumatism|October 3, 2000
Localization of a gene for familial recurrent arthritisC A Wise, L B Bennett, V Pascual, et al.
Spine|September 14, 2000
Localization of susceptibility to familial idiopathic scoliosisC A Wise, R Barnes, J Gillum, et al.
Journal of Occupational Rehabilitation|November 19, 2013
Reliability of a digital electroneurometer for the determination of motor latency of the median nerveT M Cook, J C Rosecrance, S J Brokman, et al.
Journal of Medical Genetics|April 16, 2002
DTDST mutations are not a frequent cause of idiopathic talipes equinovarus (club foot)L Bonafé, S H Blanton, A Scott, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|March 1, 1992
Subcutaneous tocolytic infusion therapy for patients at very high risk for preterm birthJ R Allbert, C A Wise, C H Lou, et al.
American Journal of Human Genetics|October 1, 1993
Molecular analyses of unrelated Charcot-Marie-Tooth (CMT) disease patients suggest a high frequency of the CMTIA duplicationC A Wise, C A Garcia, S N Davis, et al.
Progress in Clinical and Biological Research|January 1, 1993
Gene dosage as a mechanism for a common autosomal dominant peripheral neuropathy: Charcot-Marie-Tooth disease type 1AB B Roa, C A Garcia, C A Wise, et al.
Methods in Enzymology|January 1, 1996
Genetic and biochemical approaches for analysis of mitochondrial RNase P from Saccharomyces cerevisiaeK R Groom, Y L Dang, G J Gao, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1997
TCOF1 gene encodes a putative nucleolar phosphoprotein that exhibits mutations in Treacher Collins Syndrome throughout its coding regionC A Wise, L C Chiang, W A Paznekas, et al.
Pageof 3