M M Shoukri|G M Lathrop - JoVE Visualize

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Human Heredity|November 1, 1994

Genetic analysis combining path analysis with regressive models: the TAU model of multifactorial transmissionZ Li, G E Bonney, G M Lathrop, et al.

American Journal of Human Genetics|March 1, 1983

Evaluating pedigree data. I. The estimation of pedigree error in the presence of marker mistypingG M Lathrop, A B Hooper, J W Huntsman, et al.

Preventive Veterinary Medicine|October 24, 1998

Investigating potential risk factors for seasonal variation: an example using graphical and spectral analysis methods based on the production of milk components in dairy cattleJ M Sargeant, M M Shoukri, S W Martin, et al.

Human Heredity|January 1, 1983

Evaluating pedigree data. II. Identifying the cause of error in families with inconsistenciesG M Lathrop, J W Huntsman, A B Hooper, et al.

Proceedings of the National Academy of Sciences of the United States of America|September 1, 1990

Simultaneous localization of cosmids and chromosome R-banding by fluorescence microscopy: application to regional mapping of human chromosome 11D Cherif, C Julier, O Delattre, et al.

Clinical Genetics|December 1, 1989

Multipoint linkage mapping of the Xq25-q26 region in a family affected by the X-linked lymphoproliferative syndromeB S Sylla, Q Wang, D Hayoz, et al.

Canadian Journal of Veterinary Research = Revue Canadienne De Recherche Veterinaire|September 10, 1999

An epidemiologic study of disease in 32 registered Holstein dairy herds in British ColumbiaR T van Dorp, S W Martin, M M Shoukri, et al.

Nature Genetics|August 10, 2000

EIF2AK3, encoding translation initiation factor 2-alpha kinase 3, is mutated in patients with Wolcott-Rallison syndromeM Delépine, M Nicolino, T Barrett, et al.

American Journal of Human Genetics|September 1, 1990

Combined segregation and linkage analysis of genetic hemochromatosis using affection status, serum iron, and HLAI B Borecki, G M Lathrop, G E Bonney, et al.

American Journal of Human Genetics|October 23, 1997

Familial infantile convulsions and paroxysmal choreoathetosis: a new neurological syndrome linked to the pericentromeric region of human chromosome 16P Szepetowski, J Rochette, P Berquin, et al.

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Showing results (41-50 of 115) with videos related to

Sort By:

Pageof 12

Human Heredity|November 1, 1994

Genetic analysis combining path analysis with regressive models: the TAU model of multifactorial transmissionZ Li, G E Bonney, G M Lathrop, et al.

American Journal of Human Genetics|March 1, 1983

Evaluating pedigree data. I. The estimation of pedigree error in the presence of marker mistypingG M Lathrop, A B Hooper, J W Huntsman, et al.

Preventive Veterinary Medicine|October 24, 1998

Investigating potential risk factors for seasonal variation: an example using graphical and spectral analysis methods based on the production of milk components in dairy cattleJ M Sargeant, M M Shoukri, S W Martin, et al.

Human Heredity|January 1, 1983

Evaluating pedigree data. II. Identifying the cause of error in families with inconsistenciesG M Lathrop, J W Huntsman, A B Hooper, et al.

Proceedings of the National Academy of Sciences of the United States of America|September 1, 1990

Simultaneous localization of cosmids and chromosome R-banding by fluorescence microscopy: application to regional mapping of human chromosome 11D Cherif, C Julier, O Delattre, et al.

Clinical Genetics|December 1, 1989

Multipoint linkage mapping of the Xq25-q26 region in a family affected by the X-linked lymphoproliferative syndromeB S Sylla, Q Wang, D Hayoz, et al.

Canadian Journal of Veterinary Research = Revue Canadienne De Recherche Veterinaire|September 10, 1999

An epidemiologic study of disease in 32 registered Holstein dairy herds in British ColumbiaR T van Dorp, S W Martin, M M Shoukri, et al.

Nature Genetics|August 10, 2000

EIF2AK3, encoding translation initiation factor 2-alpha kinase 3, is mutated in patients with Wolcott-Rallison syndromeM Delépine, M Nicolino, T Barrett, et al.

American Journal of Human Genetics|September 1, 1990

Combined segregation and linkage analysis of genetic hemochromatosis using affection status, serum iron, and HLAI B Borecki, G M Lathrop, G E Bonney, et al.

American Journal of Human Genetics|October 23, 1997

Familial infantile convulsions and paroxysmal choreoathetosis: a new neurological syndrome linked to the pericentromeric region of human chromosome 16P Szepetowski, J Rochette, P Berquin, et al.

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