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G K Suthers

Showing results (21-30 of 29) with videos related to

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American Journal of Human Genetics|August 1, 1990
Physical mapping of new DNA probes near the fragile X mutation (FRAXA) by using a panel of cell linesG K Suthers, V J Hyland, D F Callen, et al.
Human Genetics|February 1, 1990
Probe, VK5B, is located in the same interval as the autosomal dominant adult polycystic kidney disease locus, PKD1V J Hyland, G K Suthers, K Friend, et al.
Nature|December 10, 1992
Primary structure of dystrophin-related proteinJ M Tinsley, D J Blake, A Roche, et al.
Genomics|January 1, 1991
Genetic mapping of new RFLPs at Xq27-q28G K Suthers, I Oberlé, J Nancarrow, et al.
Human Genetics|March 1, 1991
Frequent deletions at Xq28 indicate genetic heterogeneity in Hunter syndromeP J Wilson, G K Suthers, D F Callen, et al.
Genomics|July 1, 1991
Linkage homogeneity near the fragile X locus in normal and fragile X familiesG K Suthers, J C Mulley, M A Voelckel, et al.
Science (New York, N.Y.)|December 8, 1989
A new DNA marker tightly linked to the fragile X locus (FRAXA)G K Suthers, D F Callen, V J Hyland, et al.
American Journal of Human Genetics|March 1, 1991
Genetic mapping of new DNA probes at Xq27 defines a strategy for DNA studies in the fragile X syndromeG K Suthers, J C Mulley, M A Voelckel, et al.
Gut|August 5, 2011
Gastric adenocarcinoma and proximal polyposis of the stomach (GAPPS): a new autosomal dominant syndromeD L Worthley, K D Phillips, N Wayte, et al.
Pageof 3

Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
American Journal of Human Genetics|August 1, 1990
Physical mapping of new DNA probes near the fragile X mutation (FRAXA) by using a panel of cell linesG K Suthers, V J Hyland, D F Callen, et al.
Human Genetics|February 1, 1990
Probe, VK5B, is located in the same interval as the autosomal dominant adult polycystic kidney disease locus, PKD1V J Hyland, G K Suthers, K Friend, et al.
Nature|December 10, 1992
Primary structure of dystrophin-related proteinJ M Tinsley, D J Blake, A Roche, et al.
Genomics|January 1, 1991
Genetic mapping of new RFLPs at Xq27-q28G K Suthers, I Oberlé, J Nancarrow, et al.
Human Genetics|March 1, 1991
Frequent deletions at Xq28 indicate genetic heterogeneity in Hunter syndromeP J Wilson, G K Suthers, D F Callen, et al.
Genomics|July 1, 1991
Linkage homogeneity near the fragile X locus in normal and fragile X familiesG K Suthers, J C Mulley, M A Voelckel, et al.
Science (New York, N.Y.)|December 8, 1989
A new DNA marker tightly linked to the fragile X locus (FRAXA)G K Suthers, D F Callen, V J Hyland, et al.
American Journal of Human Genetics|March 1, 1991
Genetic mapping of new DNA probes at Xq27 defines a strategy for DNA studies in the fragile X syndromeG K Suthers, J C Mulley, M A Voelckel, et al.
Gut|August 5, 2011
Gastric adenocarcinoma and proximal polyposis of the stomach (GAPPS): a new autosomal dominant syndromeD L Worthley, K D Phillips, N Wayte, et al.
Pageof 3