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G K Suthers

Showing results (11-20 of 29) with videos related to

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American Journal of Human Genetics|November 1, 1992
X-linked alpha-thalassemia/mental retardation (ATR-X) syndrome: localization to Xq12-q21.31 by X inactivation and linkage analysisR J Gibbons, G K Suthers, A O Wilkie, et al.
Clinical Dysmorphology|July 12, 2001
Microlissencephaly with cardiac, spinal and urogenital defectsR J Gardner, R Savarirayan, K B Dunne, et al.
Human Molecular Genetics|October 13, 2000
New mutations in MID1 provide support for loss of function as the cause of X-linked Opitz syndromeT C Cox, L R Allen, L L Cox, et al.
Human Genetics|February 1, 1997
Mutation detection in FGFR2 craniosynostosis syndromesG E Hollway, G K Suthers, E A Haan, et al.
Genomics|November 1, 1991
Addition of MT, D16S10, D16S4, and D16S91 to the linkage map within 16q12.1-q22.1H M Kozman, A K Gedeon, S Whitmore, et al.
American Journal of Human Genetics|March 1, 1992
High-resolution genetic map around the spinal muscular atrophy (SMA) locus on chromosome 5K E Morrison, R J Daniels, G K Suthers, et al.
British Journal of Cancer|August 22, 2002
Tailoring communication in consultations with women from high risk breast cancer familiesE A Lobb, P N Butow, B Meiser, et al.
American Journal of Human Genetics|January 1, 1991
Four chromosomal breakpoints and four new probes mark out a 10-cM region encompassing the fragile-X locus (FRAXA)F Rousseau, A Vincent, S Rivella, et al.
Human Genetics|September 1, 1993
Two novel microsatellite markers for prenatal prediction of spinal muscular atrophy (SMA)K E Morrison, R J Daniels, G K Suthers, et al.
Journal of Medical Genetics|March 1, 1992
Prenatal prediction of spinal muscular atrophyR J Daniels, G K Suthers, K E Morrison, et al.
Pageof 3

Showing results (11-20 of 29) with videos related to

Sort By:
Pageof 3
American Journal of Human Genetics|November 1, 1992
X-linked alpha-thalassemia/mental retardation (ATR-X) syndrome: localization to Xq12-q21.31 by X inactivation and linkage analysisR J Gibbons, G K Suthers, A O Wilkie, et al.
Clinical Dysmorphology|July 12, 2001
Microlissencephaly with cardiac, spinal and urogenital defectsR J Gardner, R Savarirayan, K B Dunne, et al.
Human Molecular Genetics|October 13, 2000
New mutations in MID1 provide support for loss of function as the cause of X-linked Opitz syndromeT C Cox, L R Allen, L L Cox, et al.
Human Genetics|February 1, 1997
Mutation detection in FGFR2 craniosynostosis syndromesG E Hollway, G K Suthers, E A Haan, et al.
Genomics|November 1, 1991
Addition of MT, D16S10, D16S4, and D16S91 to the linkage map within 16q12.1-q22.1H M Kozman, A K Gedeon, S Whitmore, et al.
American Journal of Human Genetics|March 1, 1992
High-resolution genetic map around the spinal muscular atrophy (SMA) locus on chromosome 5K E Morrison, R J Daniels, G K Suthers, et al.
British Journal of Cancer|August 22, 2002
Tailoring communication in consultations with women from high risk breast cancer familiesE A Lobb, P N Butow, B Meiser, et al.
American Journal of Human Genetics|January 1, 1991
Four chromosomal breakpoints and four new probes mark out a 10-cM region encompassing the fragile-X locus (FRAXA)F Rousseau, A Vincent, S Rivella, et al.
Human Genetics|September 1, 1993
Two novel microsatellite markers for prenatal prediction of spinal muscular atrophy (SMA)K E Morrison, R J Daniels, G K Suthers, et al.
Journal of Medical Genetics|March 1, 1992
Prenatal prediction of spinal muscular atrophyR J Daniels, G K Suthers, K E Morrison, et al.
Pageof 3