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Acta Neuropathologica
|
January 1, 1985
Cerebellar plaques in familial Alzheimer's disease (Gerstmann-Sträussler-Scheinker variant?)
B Azzarelli, J Muller, B Ghetti, et al.
Human Heredity
|
January 1, 1982
Absence of close linkage between acute intermittent porphyria and the ABO, Rh, P, acid phosphatase, Pr, orosmucoid and pepsinogen loci
K S Dean, P M Conneally, S Sassa, et al.
The New England Journal of Medicine
|
October 30, 1986
Linkage of the G8 marker on chromosome 4 to Huntington's disease in a large American black family
T D Bird, J Hewitt, P M Conneally, et al.
Birth Defects Original Article Series
|
January 1, 1975
Holoprosencephaly: birth data, benetic and demographic analyses of 30 families
E Roach, W Demyer, P M Conneally, et al.
American Journal of Medical Genetics
|
October 1, 1986
Molecular detection of carriers of hereditary amyloidosis in a Swedish-American family
M R Wallace, P M Conneally, G L Long, et al.
Clinical Genetics
|
August 1, 1987
Suggestion of linkage of a major locus for nonsyndromic orofacial cleft with F13A and tentative assignment to chromosome 6
H Eiberg, D Bixler, L S Nielsen, et al.
Human Genetics
|
January 1, 1981
The genetic structure of the Kuwaiti population. I. Distribution of 17 markers with genetic distance analysis
K E Al-Nassar, P M Conneally, C G Palmer, et al.
Hypertension (Dallas, Tex. : 1979)
|
September 1, 1979
Association of blood groups with essential and secondary hypertension. A possible association of the MNS system
J Z Miller, C E Grim, P M Conneally, et al.
Journal of Medical Genetics
|
April 1, 1991
Patterns of inheritance of the symptoms of Huntington's disease suggestive of an effect of genomic imprinting
R M Ridley, C D Frith, L A Farrer, et al.
Journal of Medical Genetics
|
September 1, 1988
Considerations in using linkage analysis as a presymptomatic test for Huntington's disease
L A Farrer, R H Myers, L A Cupples, et al.
Page
of 19
Search research articles
Search
Showing results (51-60 of 186) with videos related to
Sort By:
Page
of 19
Acta Neuropathologica
|
January 1, 1985
Cerebellar plaques in familial Alzheimer's disease (Gerstmann-Sträussler-Scheinker variant?)
B Azzarelli, J Muller, B Ghetti, et al.
Human Heredity
|
January 1, 1982
Absence of close linkage between acute intermittent porphyria and the ABO, Rh, P, acid phosphatase, Pr, orosmucoid and pepsinogen loci
K S Dean, P M Conneally, S Sassa, et al.
The New England Journal of Medicine
|
October 30, 1986
Linkage of the G8 marker on chromosome 4 to Huntington's disease in a large American black family
T D Bird, J Hewitt, P M Conneally, et al.
Birth Defects Original Article Series
|
January 1, 1975
Holoprosencephaly: birth data, benetic and demographic analyses of 30 families
E Roach, W Demyer, P M Conneally, et al.
American Journal of Medical Genetics
|
October 1, 1986
Molecular detection of carriers of hereditary amyloidosis in a Swedish-American family
M R Wallace, P M Conneally, G L Long, et al.
Clinical Genetics
|
August 1, 1987
Suggestion of linkage of a major locus for nonsyndromic orofacial cleft with F13A and tentative assignment to chromosome 6
H Eiberg, D Bixler, L S Nielsen, et al.
Human Genetics
|
January 1, 1981
The genetic structure of the Kuwaiti population. I. Distribution of 17 markers with genetic distance analysis
K E Al-Nassar, P M Conneally, C G Palmer, et al.
Hypertension (Dallas, Tex. : 1979)
|
September 1, 1979
Association of blood groups with essential and secondary hypertension. A possible association of the MNS system
J Z Miller, C E Grim, P M Conneally, et al.
Journal of Medical Genetics
|
April 1, 1991
Patterns of inheritance of the symptoms of Huntington's disease suggestive of an effect of genomic imprinting
R M Ridley, C D Frith, L A Farrer, et al.
Journal of Medical Genetics
|
September 1, 1988
Considerations in using linkage analysis as a presymptomatic test for Huntington's disease
L A Farrer, R H Myers, L A Cupples, et al.
Page
of 19