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P F Chance

Showing results (21-30 of 78) with videos related to

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American Journal of Human Genetics|February 1, 1994
Refined genetic mapping of X-linked Charcot-Marie-Tooth neuropathyP R Fain, D F Barker, P F Chance
JAMA|November 17, 1993
Inherited primary peripheral neuropathies. Molecular genetics and clinical implications of CMT1A and HNPPJ R Lupski, P F Chance, C A Garcia
American Journal of Medical Genetics|September 19, 1997
Clinical and molecular analysis in Joubert syndromeJ E Pellegrino, M W Lensch, M Muenke, et al.
Physical Medicine and Rehabilitation Clinics of North America|January 20, 1999
Molecular basis of neuromuscular diseasesP F Chance, T Ashizawa, E P Hoffman, et al.
Human Genetics|May 14, 1999
Mapping of the kinesin-related gene ATSV to chromosome 2q37M P Keller, B A Seifried, B A Rabin, et al.
Neurology|February 1, 1987
Genetic linkage relationships of Charcot-Marie-Tooth disease (HMSN-Ib) to chromosome 1 markersP F Chance, J C Murray, T D Bird, et al.
American Journal of Medical Genetics|May 3, 1996
Cytogenetic and molecular analysis in trisomy 12pT L Allen, A R Brothman, J C Carey, et al.
Neurology|December 12, 2001
Craniofacial and cutaneous findings expand the phenotype of hereditary neuralgic amyotrophyP Y Jeannet, G D Watts, T D Bird, et al.
Neurology|October 1, 1992
Analysis of the DNA duplication 17p11.2 in Charcot-Marie-Tooth neuropathy type 1 pedigrees: additional evidence for a third autosomal CMT1 locusP F Chance, N Matsunami, W Lensch, et al.
Muscle & Nerve|March 1, 1997
Familial autosomal-dominant carpal tunnel syndrome presenting in a 5-year-old-case report and review of the literatureA G Vadasz, P F Chance, L G Epstein, et al.
Pageof 8

Showing results (21-30 of 78) with videos related to

Sort By:
Pageof 8
American Journal of Human Genetics|February 1, 1994
Refined genetic mapping of X-linked Charcot-Marie-Tooth neuropathyP R Fain, D F Barker, P F Chance
JAMA|November 17, 1993
Inherited primary peripheral neuropathies. Molecular genetics and clinical implications of CMT1A and HNPPJ R Lupski, P F Chance, C A Garcia
American Journal of Medical Genetics|September 19, 1997
Clinical and molecular analysis in Joubert syndromeJ E Pellegrino, M W Lensch, M Muenke, et al.
Physical Medicine and Rehabilitation Clinics of North America|January 20, 1999
Molecular basis of neuromuscular diseasesP F Chance, T Ashizawa, E P Hoffman, et al.
Human Genetics|May 14, 1999
Mapping of the kinesin-related gene ATSV to chromosome 2q37M P Keller, B A Seifried, B A Rabin, et al.
Neurology|February 1, 1987
Genetic linkage relationships of Charcot-Marie-Tooth disease (HMSN-Ib) to chromosome 1 markersP F Chance, J C Murray, T D Bird, et al.
American Journal of Medical Genetics|May 3, 1996
Cytogenetic and molecular analysis in trisomy 12pT L Allen, A R Brothman, J C Carey, et al.
Neurology|December 12, 2001
Craniofacial and cutaneous findings expand the phenotype of hereditary neuralgic amyotrophyP Y Jeannet, G D Watts, T D Bird, et al.
Neurology|October 1, 1992
Analysis of the DNA duplication 17p11.2 in Charcot-Marie-Tooth neuropathy type 1 pedigrees: additional evidence for a third autosomal CMT1 locusP F Chance, N Matsunami, W Lensch, et al.
Muscle & Nerve|March 1, 1997
Familial autosomal-dominant carpal tunnel syndrome presenting in a 5-year-old-case report and review of the literatureA G Vadasz, P F Chance, L G Epstein, et al.
Pageof 8