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J M Vance

Showing results (61-70 of 104) with videos related to

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American Journal of Human Genetics|February 15, 2001
A duplication in chromosome 4q35 is associated with hereditary benign intraepithelial dyskeratosisR R Allingham, B Seo, E Rampersaud, et al.
Experimental Neurology|May 1, 1989
Linkage of Charcot-Marie-Tooth neuropathy type 1a to chromosome 17J M Vance, G A Nicholson, L H Yamaoka, et al.
Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1996
Protein: protein interactions in Alzheimer's disease and the CAG triplet repeat diseasesW J Strittmatter, J R Burke, V S DeSerrano, et al.
Annals of Neurology|November 1, 1996
Confirmation of linkage of oculopharyngeal muscular dystrophy to chromosome 14q11.2-q13J M Stajich, J M Gilchrist, F Lennon, et al.
American Journal of Human Genetics|June 1, 1992
Confirmation of genetic heterogeneity in limb-girdle muscular dystrophy: linkage of an autosomal dominant form to chromosome 5qM C Speer, L H Yamaoka, J H Gilchrist, et al.
Genomics|November 26, 1998
Use of a CEPH meiotic breakpoint panel to refine the locus of limb-girdle muscular dystrophy type 1A (LGMD1A) to a 2-Mb interval on 5q31L Bartoloni, S K Horrigan, K D Viles, et al.
American Journal of Human Genetics|January 1, 1989
Genetic linkage mapping of chromosome 17 markers and neurofibromatosis type IJ M Vance, M A Pericak-Vance, L H Yamaoka, et al.
Human Genetics|April 1, 1998
Quantitative DNA pooling to increase the efficiency of linkage analysis in autosomal dominant diseaseK F Damji, C J Gallione, R R Allingham, et al.
Genomics|December 1, 1987
Genetic linkage studies of chromosome 17 RFLPs in von Recklinghausen neurofibromatosis (NF1)M A Pericak-Vance, L H Yamaoka, J M Vance, et al.
Journal of Medical Genetics|September 1, 1987
Linkage studies in peripheral neurofibromatosisM A Pericak-Vance, L H Yamaoka, J M Vance, et al.
Pageof 11

Showing results (61-70 of 104) with videos related to

Sort By:
Pageof 11
American Journal of Human Genetics|February 15, 2001
A duplication in chromosome 4q35 is associated with hereditary benign intraepithelial dyskeratosisR R Allingham, B Seo, E Rampersaud, et al.
Experimental Neurology|May 1, 1989
Linkage of Charcot-Marie-Tooth neuropathy type 1a to chromosome 17J M Vance, G A Nicholson, L H Yamaoka, et al.
Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1996
Protein: protein interactions in Alzheimer's disease and the CAG triplet repeat diseasesW J Strittmatter, J R Burke, V S DeSerrano, et al.
Annals of Neurology|November 1, 1996
Confirmation of linkage of oculopharyngeal muscular dystrophy to chromosome 14q11.2-q13J M Stajich, J M Gilchrist, F Lennon, et al.
American Journal of Human Genetics|June 1, 1992
Confirmation of genetic heterogeneity in limb-girdle muscular dystrophy: linkage of an autosomal dominant form to chromosome 5qM C Speer, L H Yamaoka, J H Gilchrist, et al.
Genomics|November 26, 1998
Use of a CEPH meiotic breakpoint panel to refine the locus of limb-girdle muscular dystrophy type 1A (LGMD1A) to a 2-Mb interval on 5q31L Bartoloni, S K Horrigan, K D Viles, et al.
American Journal of Human Genetics|January 1, 1989
Genetic linkage mapping of chromosome 17 markers and neurofibromatosis type IJ M Vance, M A Pericak-Vance, L H Yamaoka, et al.
Human Genetics|April 1, 1998
Quantitative DNA pooling to increase the efficiency of linkage analysis in autosomal dominant diseaseK F Damji, C J Gallione, R R Allingham, et al.
Genomics|December 1, 1987
Genetic linkage studies of chromosome 17 RFLPs in von Recklinghausen neurofibromatosis (NF1)M A Pericak-Vance, L H Yamaoka, J M Vance, et al.
Journal of Medical Genetics|September 1, 1987
Linkage studies in peripheral neurofibromatosisM A Pericak-Vance, L H Yamaoka, J M Vance, et al.
Pageof 11