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The Journal of Pediatrics
|
December 1, 1994
Genetic risk factors for melanoma in children
E M Petty
Clinical Genetics
|
August 21, 2008
MicroRNAs in development and disease
A E Erson, E M Petty
Clinical Chemistry
|
January 1, 1997
BRCA1 mutation testing: controversies and challenges
E M Petty, A A Killeen
Clinics in Laboratory Medicine
|
March 1, 1996
Risk assessment and presymptomatic molecular diagnosis in hereditary breast cancer
S D Merajver, E M Petty
Clinical Genetics
|
March 19, 2010
Conquering the complex world of human septins: implications for health and disease
E A Peterson, E M Petty
Journal of Medical Genetics
|
July 13, 2002
Novel autosomal dominant mandibulofacial dysostosis with ptosis: clinical description and exclusion of TCOF1
P 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 community
K K Milner, T Han, E M Petty
Nucleic Acids Research
|
February 11, 1991
Ornithine transcarbamylase polymorphism detected by PCR introduction of DraI site
E M Petty, R Carstens, A E Bale
American Journal of Medical Genetics
|
March 1, 1990
Previously unrecognized congenital progeroid disorder
E 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 F508
E M Petty, E Gold, A E Bale
Page
of 5
Search research articles
Search
Showing results (1-10 of 44) with videos related to
Sort By:
Page
of 5
The Journal of Pediatrics
|
December 1, 1994
Genetic risk factors for melanoma in children
E M Petty
Clinical Genetics
|
August 21, 2008
MicroRNAs in development and disease
A E Erson, E M Petty
Clinical Chemistry
|
January 1, 1997
BRCA1 mutation testing: controversies and challenges
E M Petty, A A Killeen
Clinics in Laboratory Medicine
|
March 1, 1996
Risk assessment and presymptomatic molecular diagnosis in hereditary breast cancer
S D Merajver, E M Petty
Clinical Genetics
|
March 19, 2010
Conquering the complex world of human septins: implications for health and disease
E A Peterson, E M Petty
Journal of Medical Genetics
|
July 13, 2002
Novel autosomal dominant mandibulofacial dysostosis with ptosis: clinical description and exclusion of TCOF1
P 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 community
K K Milner, T Han, E M Petty
Nucleic Acids Research
|
February 11, 1991
Ornithine transcarbamylase polymorphism detected by PCR introduction of DraI site
E M Petty, R Carstens, A E Bale
American Journal of Medical Genetics
|
March 1, 1990
Previously unrecognized congenital progeroid disorder
E 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 F508
E M Petty, E Gold, A E Bale
Page
of 5