Search research articles
Contact Us
Filters
Showing results (91-100 of 186) with videos related to
Page
of 19
Sort By:
Connective Tissue Research
|
January 1, 1993
Limb-girdle muscular dystrophy is closely linked to the fibrillin locus on chromosome 15
M Velinov, M Sarfarazi, K Young, et al.
Clinical Genetics
|
September 1, 1994
Possible localization of a major gene for cleft lip and palate to 4q
S 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 studies
P 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 hypertension
J 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 esophagus
D 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 genes
J L Haines, L Ozelius, P St George-Hyslop, et al.
Cytogenetics and Cell Genetics
|
January 1, 1978
Genetic linkage studies in Huntington disease
M 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 Reporting
P 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 carriers
S C Kirkwood, E Siemers, J C Stout, et al.
Clinical Genetics
|
August 1, 1981
Carrier detection in Sanfilippo syndrome type B: report of six families
J M Vance, P M Conneally, R S Wappner, et al.
Page
of 19
Search research articles
Search
Showing results (91-100 of 186) with videos related to
Sort By:
Page
of 19
Connective Tissue Research
|
January 1, 1993
Limb-girdle muscular dystrophy is closely linked to the fibrillin locus on chromosome 15
M Velinov, M Sarfarazi, K Young, et al.
Clinical Genetics
|
September 1, 1994
Possible localization of a major gene for cleft lip and palate to 4q
S 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 studies
P 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 hypertension
J 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 esophagus
D 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 genes
J L Haines, L Ozelius, P St George-Hyslop, et al.
Cytogenetics and Cell Genetics
|
January 1, 1978
Genetic linkage studies in Huntington disease
M 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 Reporting
P 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 carriers
S C Kirkwood, E Siemers, J C Stout, et al.
Clinical Genetics
|
August 1, 1981
Carrier detection in Sanfilippo syndrome type B: report of six families
J M Vance, P M Conneally, R S Wappner, et al.
Page
of 19