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Scholarly Works (4 results)
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Article
Peer Reviewed
Clinical features in a unique family with autosomal dominant limb-girdle muscular dystrophy and paget disease of bone.
Kimonis, VE
;
Kovach, M
;
Khardori, R
;
Gelber, DA
UC Irvine Previously Published Works
(1999)
Article
Peer Reviewed
Heterogeneity in familial autosomal dominant Paget disease of bone and muscular dystrophy.
Waggoner, B
;
Kimonis, VE
;
Kovach, MJ
;
Gelber, DA
;
Khardori, R
UC Irvine Previously Published Works
(2000)
Article
Peer Reviewed
Clinical and molecular studies in a large unique family with Limb-Girdle Muscular Dystrophy and Paget Disease of Bone.
Kimonis, VE
;
Kovach, MJ
;
Leal, S
;
Waggoner, B
;
Khardori, R
;
Gelber, D
UC Irvine Previously Published Works
(2000)
Article
Peer Reviewed
Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder: Hereditary inclusion body myopathy, Paget disease of bone and frontotemporal dementia in four families.
Kimonis, VE
;
Kovach, M
;
Waggoner, B
;
Leal, SM
;
Simmons, Z
;
Khardori, R
;
Whyte, MP
;
Pestronk, A
UC Irvine Previously Published Works
(2001)
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