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Results of search for 'au:"Differ, A M"'
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Authors
Abbott, M H
Almqvist, E
Biancalana, V
Bobrow, M
Cassiman, J J
Chotai, K
Coles, R
Connarty, M
Crauford, D
Curtis, A
Curtis, D
Davidson, M J
Differ, A M
Dode, C
Dodge, A
Franz, M L
Frontali, M
Graham, C A
Harper, P S
Hayden, M R
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Adult
Age of Onset
Aged
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Creatine Kinase
Dementia
Deoxyribonucleases, Type II Site-Specific
Depression
Female
Haplotypes
Humans
Huntington Disease
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Middle Aged
Minisatellite Repeats
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Myotonic Dystrophy
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Your search returned 3 results.
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1.
A novel NcoI polymorphism creates a fifth haplotype in the 3' untranslated region of CKM.
[electronic resource]
by
Differ, A M
Bobrow, M
Mathew, C G
Producer:
19920929
In:
Human genetics
vol. 89
Online resources:
Available from publisher's website
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No items available.
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2.
Familial psychiatric presentation of Huntington's disease.
[electronic resource]
by
Lovestone, S
Hodgson, S
Sham, P
Differ, A M
Levy, R
Producer:
19970512
In:
Journal of medical genetics
vol. 33
Online resources:
Available from publisher's website
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No items available.
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3.
Phenotypic characterization of individuals with 30-40 CAG repeats in the Huntington disease (HD) gene reveals HD cases with 36 repeats and apparently normal elderly individuals with 36-39 repeats.
[electronic resource]
by
Rubinsztein, D C
Leggo, J
Coles, R
Almqvist, E
Biancalana, V
Cassiman, J J
Chotai, K
Connarty, M
Crauford, D
Curtis, A
Curtis, D
Davidson, M J
Differ, A M
Dode, C
Dodge, A
Frontali, M
Ranen, N G
Stine, O C
Sherr, M
Abbott, M H
Franz, M L
Graham, C A
Harper, P S
Hedreen, J C
Hayden, M R
Producer:
19960801
In:
American journal of human genetics
vol. 59
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No items available.
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