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P M Conneally

Showing results (91-100 of 186) with videos related to

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Connective Tissue Research|January 1, 1993
Limb-girdle muscular dystrophy is closely linked to the fibrillin locus on chromosome 15M Velinov, M Sarfarazi, K Young, et al.
Clinical Genetics|September 1, 1994
Possible localization of a major gene for cleft lip and palate to 4qS Beiraghi, T Foroud, S Diouhy, et al.
Cytogenetics and Cell Genetics|January 1, 1978
Confirmation of genetic heterogeneity in autosomal dominant forms of congenital cataracts from linkage studiesP M Conneally, A F Wilson, A D Merritt, et al.
American Journal of Respiratory and Critical Care Medicine|July 1, 1995
Genetic anticipation and abnormal gender ratio at birth in familial primary pulmonary hypertensionJ E Loyd, M G Butler, T M Foroud, et al.
Annals of Internal Medicine|July 1, 1985
Familial gastroesophageal reflux and development of Barrett's esophagusD W Crabb, M A Berk, T R Hall, et al.
Genetic Epidemiology|January 1, 1988
Partial linkage map of chromosome 13q in the region of the Wilson disease and retinoblastoma genesJ L Haines, L Ozelius, P St George-Hyslop, et al.
Cytogenetics and Cell Genetics|January 1, 1978
Genetic linkage studies in Huntington diseaseM A Pericak-Vance, P M Conneally, A D Merritt, et al.
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.
Pageof 19

Showing results (91-100 of 186) with videos related to

Sort By:
Pageof 19
Connective Tissue Research|January 1, 1993
Limb-girdle muscular dystrophy is closely linked to the fibrillin locus on chromosome 15M Velinov, M Sarfarazi, K Young, et al.
Clinical Genetics|September 1, 1994
Possible localization of a major gene for cleft lip and palate to 4qS Beiraghi, T Foroud, S Diouhy, et al.
Cytogenetics and Cell Genetics|January 1, 1978
Confirmation of genetic heterogeneity in autosomal dominant forms of congenital cataracts from linkage studiesP M Conneally, A F Wilson, A D Merritt, et al.
American Journal of Respiratory and Critical Care Medicine|July 1, 1995
Genetic anticipation and abnormal gender ratio at birth in familial primary pulmonary hypertensionJ E Loyd, M G Butler, T M Foroud, et al.
Annals of Internal Medicine|July 1, 1985
Familial gastroesophageal reflux and development of Barrett's esophagusD W Crabb, M A Berk, T R Hall, et al.
Genetic Epidemiology|January 1, 1988
Partial linkage map of chromosome 13q in the region of the Wilson disease and retinoblastoma genesJ L Haines, L Ozelius, P St George-Hyslop, et al.
Cytogenetics and Cell Genetics|January 1, 1978
Genetic linkage studies in Huntington diseaseM A Pericak-Vance, P M Conneally, A D Merritt, et al.
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.
Pageof 19