M Pericak-Vance - JoVE Visualize

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Neurology|January 1, 1988

Clinical and genetic investigation in autosomal dominant limb-girdle muscular dystrophyJ M Gilchrist, M Pericak-Vance, L Silverman, et al.

Journal of Medical Genetics|August 1, 1989

An exclusion map for facioscapulohumeral (Landouzy-Déjérine) diseaseM Sarfarazi, M Upadhyaya, G Padberg, et al.

Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|June 1, 1996

Ocular motility in North Carolina autosomal dominant ataxiaK W Small, S C Pollock, J M Vance, et al.

Genomics|November 1, 1991

North Carolina macular dystrophy: exclusion map using RFLPs and microsatellitesK W Small, J L Weber, W Y Hung, et al.

Annals of Neurology|October 1, 1986

X-linked neuropathy: gene localization with DNA probesK H Fischbeck, N ar-Rushdi, M Pericak-Vance, et al.

Proceedings of the National Academy of Sciences of the United States of America|March 1, 1993

Apolipoprotein E: high-avidity binding to beta-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer diseaseW J Strittmatter, A M Saunders, D Schmechel, et al.

American Journal of Human Genetics|August 1, 1992

Regional mapping of facioscapulohumeral muscular dystrophy gene on 4q35: combined analysis of an international consortiumM Sarfarazi, C Wijmenga, M Upadhyaya, et al.

Australian Paediatric Journal|January 1, 1988

Update on the molecular genetics of Duchenne muscular dystrophyT Siddique, R Bartlett, M Pericak-Vance, et al.

Journal of Immunology (Baltimore, Md. : 1950)|June 22, 2000

Linkage of the CCR5 Delta 32 mutation with a functional polymorphism of CD45RAH X Liao, D C Montefiori, D D Patel, et al.

Experimental Neurology|July 1, 1994

Apolipoprotein E is present in hippocampal neurons without neurofibrillary tangles in Alzheimer's disease and in age-matched controlsS H Han, C Hulette, A M Saunders, et al.

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Showing results (1-10 of 31) with videos related to

Sort By:

Pageof 4

Neurology|January 1, 1988

Clinical and genetic investigation in autosomal dominant limb-girdle muscular dystrophyJ M Gilchrist, M Pericak-Vance, L Silverman, et al.

Journal of Medical Genetics|August 1, 1989

An exclusion map for facioscapulohumeral (Landouzy-Déjérine) diseaseM Sarfarazi, M Upadhyaya, G Padberg, et al.

Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|June 1, 1996

Ocular motility in North Carolina autosomal dominant ataxiaK W Small, S C Pollock, J M Vance, et al.

Genomics|November 1, 1991

North Carolina macular dystrophy: exclusion map using RFLPs and microsatellitesK W Small, J L Weber, W Y Hung, et al.

Annals of Neurology|October 1, 1986

X-linked neuropathy: gene localization with DNA probesK H Fischbeck, N ar-Rushdi, M Pericak-Vance, et al.

Proceedings of the National Academy of Sciences of the United States of America|March 1, 1993

Apolipoprotein E: high-avidity binding to beta-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer diseaseW J Strittmatter, A M Saunders, D Schmechel, et al.

American Journal of Human Genetics|August 1, 1992

Regional mapping of facioscapulohumeral muscular dystrophy gene on 4q35: combined analysis of an international consortiumM Sarfarazi, C Wijmenga, M Upadhyaya, et al.

Australian Paediatric Journal|January 1, 1988

Update on the molecular genetics of Duchenne muscular dystrophyT Siddique, R Bartlett, M Pericak-Vance, et al.

Journal of Immunology (Baltimore, Md. : 1950)|June 22, 2000

Linkage of the CCR5 Delta 32 mutation with a functional polymorphism of CD45RAH X Liao, D C Montefiori, D D Patel, et al.

Experimental Neurology|July 1, 1994

Apolipoprotein E is present in hippocampal neurons without neurofibrillary tangles in Alzheimer's disease and in age-matched controlsS H Han, C Hulette, A M Saunders, et al.

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