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P M MacLeod

Showing results (31-40 of 58) with videos related to

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American Journal of Medical Genetics|August 1, 1989
Growth and development in thanatophoric dysplasiaI M MacDonald, A G Hunter, P M MacLeod, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Gonadal mosaicism in a family with adrenoleukodystrophy: molecular diagnosis of carrier status among daughters of a gonadal mosaic when direct detection of the mutation is not possibleG E Graham, P M MacLeod, D P Lillicrap, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Methylcitrate in maternal urine during a pregnancy with a fetus affected with propionic acidaemiaS Aramaki, D Lehotay, W L Nyhan, et al.
Clinical Genetics|October 12, 2001
High incidence rate and absent family histories in one quarter of patients newly diagnosed with Huntington disease in British ColumbiaE W Almqvist, D S Elterman, P M MacLeod, et al.
Human Mutation|January 1, 1996
Novel mutations in the connexin 32 gene associated with X-linked Charcot-Marie tooth diseaseC C Tan, P J Ainsworth, A F Hahn, et al.
Clinical Genetics|June 1, 1986
Xp21/autosome translocations. Case report and risk for Duchenne muscular dystrophyJ J Holden, A Smith, P M MacLeod, et al.
Birth Defects Original Article Series|January 1, 1976
The neuronal ceroid lipofuscinoses in British Columbia: a clinical epidemiologic and ultrastructural studyP M MacLeod, C L Dolman, E Chang, et al.
Human Genetics|March 12, 1979
Clinical and ultrastructural heterogeneity of type IV Ehlers-Danlos syndromeP H Byers, K A Holbrook, B McGillivray, et al.
Journal of Neurogenetics|July 1, 1986
Localization of X-linked dominant Charcot-Marie-Tooth disease (CMT 2) to Xq13J Beckett, J J Holden, N E Simpson, et al.
Neurology|June 1, 1977
Progressive cerebellar ataxia, spasticity, psychomotor retardation, and hexosaminidase deficiency in a 10-year-old child: juvenile Sandhoff diseaseP M MacLeod, S Wood, J E Jan, et al.
Pageof 6

Showing results (31-40 of 58) with videos related to

Sort By:
Pageof 6
American Journal of Medical Genetics|August 1, 1989
Growth and development in thanatophoric dysplasiaI M MacDonald, A G Hunter, P M MacLeod, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Gonadal mosaicism in a family with adrenoleukodystrophy: molecular diagnosis of carrier status among daughters of a gonadal mosaic when direct detection of the mutation is not possibleG E Graham, P M MacLeod, D P Lillicrap, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Methylcitrate in maternal urine during a pregnancy with a fetus affected with propionic acidaemiaS Aramaki, D Lehotay, W L Nyhan, et al.
Clinical Genetics|October 12, 2001
High incidence rate and absent family histories in one quarter of patients newly diagnosed with Huntington disease in British ColumbiaE W Almqvist, D S Elterman, P M MacLeod, et al.
Human Mutation|January 1, 1996
Novel mutations in the connexin 32 gene associated with X-linked Charcot-Marie tooth diseaseC C Tan, P J Ainsworth, A F Hahn, et al.
Clinical Genetics|June 1, 1986
Xp21/autosome translocations. Case report and risk for Duchenne muscular dystrophyJ J Holden, A Smith, P M MacLeod, et al.
Birth Defects Original Article Series|January 1, 1976
The neuronal ceroid lipofuscinoses in British Columbia: a clinical epidemiologic and ultrastructural studyP M MacLeod, C L Dolman, E Chang, et al.
Human Genetics|March 12, 1979
Clinical and ultrastructural heterogeneity of type IV Ehlers-Danlos syndromeP H Byers, K A Holbrook, B McGillivray, et al.
Journal of Neurogenetics|July 1, 1986
Localization of X-linked dominant Charcot-Marie-Tooth disease (CMT 2) to Xq13J Beckett, J J Holden, N E Simpson, et al.
Neurology|June 1, 1977
Progressive cerebellar ataxia, spasticity, psychomotor retardation, and hexosaminidase deficiency in a 10-year-old child: juvenile Sandhoff diseaseP M MacLeod, S Wood, J E Jan, et al.
Pageof 6