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Genetic Testing
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October 24, 2007
A genetic history questionnaire-based system in primary prenatal care to screen for selected fetal disorders
Linda A Bradley, Edward M Kloza, Paula K Haddow, et al.
Genetic Testing
|
October 24, 2007
Twenty-four novel mutations in Wilson disease patients of predominantly Italian origin
Maria Barbara Lepori, Mario Lovicu, Valentina Dessi, et al.
Genetic Testing
|
November 4, 2008
One third of Japanese patients with multiple osteochondromas may have mutations in genes other than EXT1 or EXT2
Hirofumi Kojima, Takahito Wada, Hiroshi Seki, et al.
Genetic Testing
|
October 23, 2008
Nucleic acid from saliva and salivary cells for noninvasive genotyping of Crohn's disease patients
Jiwon Hong, Euphemia Leung, Alan Fraser, et al.
Genetic Testing
|
October 23, 2008
Association of smoking behavior with an odorant receptor allele telomeric to the human major histocompatibility complex
Pablo Sandro Carvalho Santos, George Füst, Zoltán Prohászka, et al.
Genetic Testing
|
August 23, 2000
Novel method for molecular detection of the two common hereditary hemochromatosis mutations
S G Kaler, J M Devaney, E L Pettit, et al.
Genetic Testing
|
December 4, 2003
Denaturing high-performance liquid chromatography for the detection of mutations and polymorphisms in UBE3A
D Bercovich, A L Beaudet
Genetic Testing
|
July 30, 2003
Issues in newborn screening
Anita Saxena
Genetic Testing
|
July 30, 2003
Connexin-30 deletion analysis in connexin-26 heterozygotes
Victoria A Stevenson, Masamichi Ito, Jeff M Milunsky
Genetic Testing
|
July 30, 2003
Absence of the Kilifi mutation in the rhinovirus-binding domain of ICAM-1 in a Caucasian population
Leen Vijgen, Mark Van Essche, Marc Van Ranst
Page
of 68
Search research articles
Search
Showing results (321-330 of 679) with videos related to
Sort By:
Page
of 68
Genetic Testing
|
October 24, 2007
A genetic history questionnaire-based system in primary prenatal care to screen for selected fetal disorders
Linda A Bradley, Edward M Kloza, Paula K Haddow, et al.
Genetic Testing
|
October 24, 2007
Twenty-four novel mutations in Wilson disease patients of predominantly Italian origin
Maria Barbara Lepori, Mario Lovicu, Valentina Dessi, et al.
Genetic Testing
|
November 4, 2008
One third of Japanese patients with multiple osteochondromas may have mutations in genes other than EXT1 or EXT2
Hirofumi Kojima, Takahito Wada, Hiroshi Seki, et al.
Genetic Testing
|
October 23, 2008
Nucleic acid from saliva and salivary cells for noninvasive genotyping of Crohn's disease patients
Jiwon Hong, Euphemia Leung, Alan Fraser, et al.
Genetic Testing
|
October 23, 2008
Association of smoking behavior with an odorant receptor allele telomeric to the human major histocompatibility complex
Pablo Sandro Carvalho Santos, George Füst, Zoltán Prohászka, et al.
Genetic Testing
|
August 23, 2000
Novel method for molecular detection of the two common hereditary hemochromatosis mutations
S G Kaler, J M Devaney, E L Pettit, et al.
Genetic Testing
|
December 4, 2003
Denaturing high-performance liquid chromatography for the detection of mutations and polymorphisms in UBE3A
D Bercovich, A L Beaudet
Genetic Testing
|
July 30, 2003
Issues in newborn screening
Anita Saxena
Genetic Testing
|
July 30, 2003
Connexin-30 deletion analysis in connexin-26 heterozygotes
Victoria A Stevenson, Masamichi Ito, Jeff M Milunsky
Genetic Testing
|
July 30, 2003
Absence of the Kilifi mutation in the rhinovirus-binding domain of ICAM-1 in a Caucasian population
Leen Vijgen, Mark Van Essche, Marc Van Ranst
Page
of 68