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A E Mackenzie

Showing results (31-40 of 56) with videos related to

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American Journal of Medical Genetics|April 1, 1992
Simpson-Golabi-Behmel syndrome associated with renal dysplasia and embryonal tumor: localization of the gene to Xqcen-q21R M Hughes-Benzie, A G Hunter, J E Allanson, et al.
Nucleic Acids Research|March 11, 1991
An insertion polymorphism identified by the probe pE0.8 (D19S115) at 19q13.3G Shutler, S Leblond, J Bailly, et al.
Human Molecular Genetics|January 1, 1994
Mapping of Simpson-Golabi-Behmel syndrome to Xq25-q27J Y Xuan, A Besner, M Ireland, et al.
Nucleic Acids Research|July 25, 1989
A BanI polymorphism identified by the probe p alpha 1.4P at 19q13.1 [D19S37]R G Korneluk, H L MacLeod, D Lahey, et al.
Frontiers in Endocrinology|June 2, 2012
GPR35 as a Novel Therapeutic TargetA E Mackenzie, J E Lappin, D L Taylor, et al.
Human Molecular Genetics|June 1, 1993
Intergenerational stability of the myotonic dystrophy protomutationJ M Barceló, M S Mahadevan, C Tsilfidis, et al.
Nucleic Acids Research|July 25, 1989
A Bsu36I RFLP detected by the chromosome 19q probe p alpha.5B [D19S36]R G Korneluk, H L MacLeod, S Leblond, et al.
Genomics|October 1, 1989
A reordering of human chromosome 19 long-arm DNA markers and identification of markers flanking the myotonic dystrophy locusR G Korneluk, A E MacKenzie, Y Nakamura, et al.
Genomics|February 1, 1989
A chromosome 19 clone from a translocation breakpoint shows close linkage and linkage disequilibrium with myotonic dystrophyR G Korneluk, H L MacLeod, T W McKeithan, et al.
American Journal of Human Genetics|June 1, 1994
Additive influence of maternal and offspring DM-kinase gene CTG repeat lengths in the genesis of congenital myotonic dystrophyJ M Barceló, M Pluscauskas, A E MacKenzie, et al.
Pageof 6

Showing results (31-40 of 56) with videos related to

Sort By:
Pageof 6
American Journal of Medical Genetics|April 1, 1992
Simpson-Golabi-Behmel syndrome associated with renal dysplasia and embryonal tumor: localization of the gene to Xqcen-q21R M Hughes-Benzie, A G Hunter, J E Allanson, et al.
Nucleic Acids Research|March 11, 1991
An insertion polymorphism identified by the probe pE0.8 (D19S115) at 19q13.3G Shutler, S Leblond, J Bailly, et al.
Human Molecular Genetics|January 1, 1994
Mapping of Simpson-Golabi-Behmel syndrome to Xq25-q27J Y Xuan, A Besner, M Ireland, et al.
Nucleic Acids Research|July 25, 1989
A BanI polymorphism identified by the probe p alpha 1.4P at 19q13.1 [D19S37]R G Korneluk, H L MacLeod, D Lahey, et al.
Frontiers in Endocrinology|June 2, 2012
GPR35 as a Novel Therapeutic TargetA E Mackenzie, J E Lappin, D L Taylor, et al.
Human Molecular Genetics|June 1, 1993
Intergenerational stability of the myotonic dystrophy protomutationJ M Barceló, M S Mahadevan, C Tsilfidis, et al.
Nucleic Acids Research|July 25, 1989
A Bsu36I RFLP detected by the chromosome 19q probe p alpha.5B [D19S36]R G Korneluk, H L MacLeod, S Leblond, et al.
Genomics|October 1, 1989
A reordering of human chromosome 19 long-arm DNA markers and identification of markers flanking the myotonic dystrophy locusR G Korneluk, A E MacKenzie, Y Nakamura, et al.
Genomics|February 1, 1989
A chromosome 19 clone from a translocation breakpoint shows close linkage and linkage disequilibrium with myotonic dystrophyR G Korneluk, H L MacLeod, T W McKeithan, et al.
American Journal of Human Genetics|June 1, 1994
Additive influence of maternal and offspring DM-kinase gene CTG repeat lengths in the genesis of congenital myotonic dystrophyJ M Barceló, M Pluscauskas, A E MacKenzie, et al.
Pageof 6