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M Conneally

Showing results (101-110 of 194) with videos related to

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Cytogenetics and Cell Genetics|January 1, 1985
Report of the Committee on Methods of Linkage Analysis and ReportingP M Conneally, J H Edwards, K K Kidd, et al.
Archives of Neurology|May 18, 1999
Longitudinal cognitive and motor changes among presymptomatic Huntington disease gene carriersS C Kirkwood, E Siemers, J C Stout, et al.
Clinical Genetics|August 1, 1981
Carrier detection in Sanfilippo syndrome type B: report of six familiesJ M Vance, P M Conneally, R S Wappner, et al.
Journal of Medical Genetics|July 13, 2002
Linkage stratification and mutation analysis at the Parkin locus identifies mutation positive Parkinson's disease familiesW C Nichols, N Pankratz, S K Uniacke, et al.
Cytogenetics and Cell Genetics|January 1, 1992
Chromosome 21 genetic linkage data set based on the Venezuelan reference pedigreeJ L Haines, J A Trofatter, R E Tanzi, et al.
Clinical Genetics|November 1, 1987
Linkage of G8 (D4S10) in two Swedish families with Huntington's diseaseG Holmgren, E W Almqvist, M Anvret, et al.
Chest|June 1, 1997
The presence of genetic anticipation suggests that the molecular basis of familial primary pulmonary hypertension may be trinucleotide repeat expansionJ E Loyd, B Slovis, J A Phillips, et al.
Clinical Genetics|December 1, 1983
Linkage analysis in von Willebrand diseaseM S Verp, R M Radvany, D Green, et al.
Nature Genetics|September 1, 1993
Charcot-Marie-Tooth neuropathy type 1B is associated with mutations of the myelin P0 geneK Hayasaka, M Himoro, W Sato, et al.
Neurology|May 12, 2004
Genes influencing Parkinson disease onset: replication of PARK3 and identification of novel lociN Pankratz, S K Uniacke, C A Halter, et al.
Pageof 20

Showing results (101-110 of 194) with videos related to

Sort By:
Pageof 20
Cytogenetics and Cell Genetics|January 1, 1985
Report of the Committee on Methods of Linkage Analysis and ReportingP M Conneally, J H Edwards, K K Kidd, et al.
Archives of Neurology|May 18, 1999
Longitudinal cognitive and motor changes among presymptomatic Huntington disease gene carriersS C Kirkwood, E Siemers, J C Stout, et al.
Clinical Genetics|August 1, 1981
Carrier detection in Sanfilippo syndrome type B: report of six familiesJ M Vance, P M Conneally, R S Wappner, et al.
Journal of Medical Genetics|July 13, 2002
Linkage stratification and mutation analysis at the Parkin locus identifies mutation positive Parkinson's disease familiesW C Nichols, N Pankratz, S K Uniacke, et al.
Cytogenetics and Cell Genetics|January 1, 1992
Chromosome 21 genetic linkage data set based on the Venezuelan reference pedigreeJ L Haines, J A Trofatter, R E Tanzi, et al.
Clinical Genetics|November 1, 1987
Linkage of G8 (D4S10) in two Swedish families with Huntington's diseaseG Holmgren, E W Almqvist, M Anvret, et al.
Chest|June 1, 1997
The presence of genetic anticipation suggests that the molecular basis of familial primary pulmonary hypertension may be trinucleotide repeat expansionJ E Loyd, B Slovis, J A Phillips, et al.
Clinical Genetics|December 1, 1983
Linkage analysis in von Willebrand diseaseM S Verp, R M Radvany, D Green, et al.
Nature Genetics|September 1, 1993
Charcot-Marie-Tooth neuropathy type 1B is associated with mutations of the myelin P0 geneK Hayasaka, M Himoro, W Sato, et al.
Neurology|May 12, 2004
Genes influencing Parkinson disease onset: replication of PARK3 and identification of novel lociN Pankratz, S K Uniacke, C A Halter, et al.
Pageof 20