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E M Petty

Showing results (1-10 of 44) with videos related to

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The Journal of Pediatrics|December 1, 1994
Genetic risk factors for melanoma in childrenE M Petty
Clinical Genetics|August 21, 2008
MicroRNAs in development and diseaseA E Erson, E M Petty
Clinical Chemistry|January 1, 1997
BRCA1 mutation testing: controversies and challengesE M Petty, A A Killeen
Clinics in Laboratory Medicine|March 1, 1996
Risk assessment and presymptomatic molecular diagnosis in hereditary breast cancerS D Merajver, E M Petty
Clinical Genetics|March 19, 2010
Conquering the complex world of human septins: implications for health and diseaseE A Peterson, E M Petty
Journal of Medical Genetics|July 13, 2002
Novel autosomal dominant mandibulofacial dysostosis with ptosis: clinical description and exclusion of TCOF1P Hedera, H V Toriello, E M Petty
Genetic Testing|September 25, 1999
Support for the availability of prenatal testing for neurological and psychiatric conditions in the psychiatric communityK K Milner, T Han, E M Petty
Nucleic Acids Research|February 11, 1991
Ornithine transcarbamylase polymorphism detected by PCR introduction of DraI siteE M Petty, R Carstens, A E Bale
American Journal of Medical Genetics|March 1, 1990
Previously unrecognized congenital progeroid disorderE M Petty, R Laxova, H R Wiedemann
Clinical Chemistry|December 1, 1992
DNA diagnosis with mutation-specific artificial methylation sites: application to rapid screening of delta F508E M Petty, E Gold, A E Bale
Pageof 5

Showing results (1-10 of 44) with videos related to

Sort By:
Pageof 5
The Journal of Pediatrics|December 1, 1994
Genetic risk factors for melanoma in childrenE M Petty
Clinical Genetics|August 21, 2008
MicroRNAs in development and diseaseA E Erson, E M Petty
Clinical Chemistry|January 1, 1997
BRCA1 mutation testing: controversies and challengesE M Petty, A A Killeen
Clinics in Laboratory Medicine|March 1, 1996
Risk assessment and presymptomatic molecular diagnosis in hereditary breast cancerS D Merajver, E M Petty
Clinical Genetics|March 19, 2010
Conquering the complex world of human septins: implications for health and diseaseE A Peterson, E M Petty
Journal of Medical Genetics|July 13, 2002
Novel autosomal dominant mandibulofacial dysostosis with ptosis: clinical description and exclusion of TCOF1P Hedera, H V Toriello, E M Petty
Genetic Testing|September 25, 1999
Support for the availability of prenatal testing for neurological and psychiatric conditions in the psychiatric communityK K Milner, T Han, E M Petty
Nucleic Acids Research|February 11, 1991
Ornithine transcarbamylase polymorphism detected by PCR introduction of DraI siteE M Petty, R Carstens, A E Bale
American Journal of Medical Genetics|March 1, 1990
Previously unrecognized congenital progeroid disorderE M Petty, R Laxova, H R Wiedemann
Clinical Chemistry|December 1, 1992
DNA diagnosis with mutation-specific artificial methylation sites: application to rapid screening of delta F508E M Petty, E Gold, A E Bale
Pageof 5