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P S Ing

Showing results (1-10 of 12) with videos related to

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Archives of Otolaryngology--Head & Neck Surgery|December 1, 1995
Hereditary hearing impairmentP S Ing
Proceedings. Symposium on Computer Applications in Medical Care|January 1, 1991
Data collection in the Great Plains Genetics Service Network: using limited funds to collect data from centers with varying resourcesP S Ing, J M Smith
Clinical Genetics|September 1, 1983
Cytogenetic studies of a patient with mosaicism of isochromosome 13q and a dicentric (Y;13) translocation showing differential centromeric activityP S Ing, S D Smith
Computers in Biology and Medicine|January 1, 1980
Human chromosome classification using discriminant analysis and Bayesian probabilityR S Ledley, P S Ing, H A Lubs
American Journal of Human Genetics|July 1, 1989
A comment on the analysis of families with prelinqual deafnessS Kimberling, S D Smith, P S Ing, et al.
Annals of the New York Academy of Sciences|January 1, 1991
National Deaf Register as a resource for hereditary deafness researchP S Ing, B M Wernimont, S D Smith, et al.
American Journal of Medical Genetics|October 1, 1989
Availability of genetic services to the deafP S Ing, M L Lempke, S D Smith, et al.
Journal of the American Academy of Child and Adolescent Psychiatry|March 1, 1990
Familial dyslexia: use of genetic linkage data to define subtypesS D Smith, B F Pennington, W J Kimberling, et al.
American Journal of Medical Genetics|March 1, 1987
Cat-eye syndrome with different marker chromosomes in a mother and daughterP S Ing, M S Lubinsky, S D Smith, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 23, 2001
The ACMG CYTO2000 subcommittee?A T Chen, P S Ing, J A Reidy, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Archives of Otolaryngology--Head & Neck Surgery|December 1, 1995
Hereditary hearing impairmentP S Ing
Proceedings. Symposium on Computer Applications in Medical Care|January 1, 1991
Data collection in the Great Plains Genetics Service Network: using limited funds to collect data from centers with varying resourcesP S Ing, J M Smith
Clinical Genetics|September 1, 1983
Cytogenetic studies of a patient with mosaicism of isochromosome 13q and a dicentric (Y;13) translocation showing differential centromeric activityP S Ing, S D Smith
Computers in Biology and Medicine|January 1, 1980
Human chromosome classification using discriminant analysis and Bayesian probabilityR S Ledley, P S Ing, H A Lubs
American Journal of Human Genetics|July 1, 1989
A comment on the analysis of families with prelinqual deafnessS Kimberling, S D Smith, P S Ing, et al.
Annals of the New York Academy of Sciences|January 1, 1991
National Deaf Register as a resource for hereditary deafness researchP S Ing, B M Wernimont, S D Smith, et al.
American Journal of Medical Genetics|October 1, 1989
Availability of genetic services to the deafP S Ing, M L Lempke, S D Smith, et al.
Journal of the American Academy of Child and Adolescent Psychiatry|March 1, 1990
Familial dyslexia: use of genetic linkage data to define subtypesS D Smith, B F Pennington, W J Kimberling, et al.
American Journal of Medical Genetics|March 1, 1987
Cat-eye syndrome with different marker chromosomes in a mother and daughterP S Ing, M S Lubinsky, S D Smith, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 23, 2001
The ACMG CYTO2000 subcommittee?A T Chen, P S Ing, J A Reidy, et al.
Pageof 2