Results
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Analysis of the functional effects of a mutation in SOD1 associated with familial amyotrophic lateral sclerosis. [electronic resource] by
- Tsuda, T
- Munthasser, S
- Fraser, P E
- Percy, M E
- Rainero, I
- Vaula, G
- Pinessi, L
- Bergamini, L
- Vignocchi, G
- McLachlan, D R
Producer: 19941101
In:
Neuron vol. 13
Availability: No items available.
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49.
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Molecular and prospective phenotypic characterization of a pedigree with familial Alzheimer's disease and a missense mutation in codon 717 of the beta-amyloid precursor protein gene. [electronic resource] by
- Karlinsky, H
- Vaula, G
- Haines, J L
- Ridgley, J
- Bergeron, C
- Mortilla, M
- Tupler, R G
- Percy, M E
- Robitaille, Y
- Noldy, N E
Producer: 19920903
In:
Neurology vol. 42
Availability: No items available.
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51.
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Carrier detection in hemophilia A: ABO blood group, multiple measurements, and application of logistic discrimination. [electronic resource] by
- Percy, M E
- Rusk, A C
- Garvey, M B
- Freedman, J J
- Teitel, J M
- Blake, P
- Carter, C
- Andrew, M
- Johnson, M
- Inwood, M
Producer: 19890505
In:
American journal of medical genetics vol. 31
Availability: No items available.
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53.
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Family with 22-derived marker chromosome and late-onset dementia of the Alzheimer type: II. Further cytogenetic analysis of the marker and characterization of the high-level repeat sequences using fluorescence in situ hybridization. [electronic resource] by
- Percy, M E
- Dearie, T G
- Jabs, E W
- Bauer, S J
- Chodakowski, B
- Somerville, M J
- Lennox, A
- McLachlan, D R
- Baldini, A
- Miller, D A
Producer: 19931007
In:
American journal of medical genetics vol. 47
Availability: No items available.
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56.
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Autoimmune thyroiditis associated with mild "subclinical" hypothyroidism in adults with Down syndrome: a comparison of patients with and without manifestations of Alzheimer disease. [electronic resource] by
- Percy, M E
- Dalton, A J
- Markovic, V D
- Crapper McLachlan, D R
- Gera, E
- Hummel, J T
- Rusk, A C
- Somerville, M J
- Andrews, D F
- Walfish, P G
Producer: 19900813
In:
American journal of medical genetics vol. 36
Availability: No items available.
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57.
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Alzheimer's disease associated with mutations in presenilin 2 is rare and variably penetrant. [electronic resource] by
- Sherrington, R
- Froelich, S
- Sorbi, S
- Campion, D
- Chi, H
- Rogaeva, E A
- Levesque, G
- Rogaev, E I
- Lin, C
- Liang, Y
- Ikeda, M
- Mar, L
- Brice, A
- Agid, Y
- Percy, M E
- Clerget-Darpoux, F
- Piacentini, S
- Marcon, G
- Nacmias, B
- Amaducci, L
- Frebourg, T
- Lannfelt, L
- Rommens, J M
- St George-Hyslop, P H
Producer: 19970116
In:
Human molecular genetics vol. 5
Availability: No items available.
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58.
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Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous disorder. [electronic resource] by
- St George-Hyslop, P H
- Haines, J L
- Farrer, L A
- Polinsky, R
- Van Broeckhoven, C
- Goate, A
- McLachlan, D R
- Orr, H
- Bruni, A C
- Sorbi, S
- Rainero, I
- Foncin, J F
- Pollen, D
- Cantu, J M
- Tupler, R
- Voskresenskaya, N
- Mayeux, R
- Growden, J
- Fried, V A
- Myers, R H
- Nee, L
- Backhovens, H
- Martin, J J
- Rossor, M
- Owen, M J
- Mullan, M
- Percy, M E
- Karlinsky, H
- Rich, S
- Heston, L
- Montesi, M
- Mortilla, M
- Nacmias, N
- Gusella, J F
- Hardy, J A
Producer: 19901011
In:
Nature vol. 347
Availability: No items available.
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