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Genetic Testing
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May 5, 2001
Chromosome 10
F Gilbert
Genetic Testing
|
August 16, 2002
Does prenatal screening for 5,10-methylenetetrahydrofolate reductase (MTHFR) mutations in high-risk neural tube defect pregnancies make sense?
Richard H Finnell, Gary M Shaw, Edward J Lammer, et al.
Genetic Testing
|
August 16, 2002
Detection of the G-->T polymorphism at the Sp1 binding site of the collagen type I alpha 1 gene by a novel ARMS-PCR method
Lucio Montanaro, Carla Renata Arciola
Genetic Testing
|
September 25, 1999
Various mutation screening techniques in the DNA mismatch repair genes hMSH2 and hMLH1
S Wahlberg, T Liu, P Lindblom, et al.
Genetic Testing
|
September 25, 1999
Neural tube defect prevalence in California (1990-1994): eliciting patterns by type of defect and maternal race/ethnicity
L B Feuchtbaum, R J Currier, S Riggle, et al.
Genetic Testing
|
September 25, 1999
Mutations in exon 3 of the PAH gene causing mild hyperphenylalaninemia
C Zekanowski, M Nowacka, M Gizewska, et al.
Genetic Testing
|
May 4, 2000
P53 mutations, polymorphisms, and haplotypes in Pakistani ethnic groups and breast cancer patients
S Khaliq, A Hameed, T Khaliq, et al.
Genetic Testing
|
May 4, 2000
Molecular analysis in Brazilian cystic fibrosis patients reveals five novel mutations
A L Bernardino, A Ferri, M R Passos-Bueno, et al.
Genetic Testing
|
August 23, 2000
Postscript: a status report on hemochromatosis population screening
F Gilbert
Genetic Testing
|
January 15, 2002
Psychological aspects of genetic counseling. XIV. Nondirectiveness and counseling skills
S Kessler
Page
of 68
Search research articles
Search
Showing results (501-510 of 679) with videos related to
Sort By:
Page
of 68
Genetic Testing
|
May 5, 2001
Chromosome 10
F Gilbert
Genetic Testing
|
August 16, 2002
Does prenatal screening for 5,10-methylenetetrahydrofolate reductase (MTHFR) mutations in high-risk neural tube defect pregnancies make sense?
Richard H Finnell, Gary M Shaw, Edward J Lammer, et al.
Genetic Testing
|
August 16, 2002
Detection of the G-->T polymorphism at the Sp1 binding site of the collagen type I alpha 1 gene by a novel ARMS-PCR method
Lucio Montanaro, Carla Renata Arciola
Genetic Testing
|
September 25, 1999
Various mutation screening techniques in the DNA mismatch repair genes hMSH2 and hMLH1
S Wahlberg, T Liu, P Lindblom, et al.
Genetic Testing
|
September 25, 1999
Neural tube defect prevalence in California (1990-1994): eliciting patterns by type of defect and maternal race/ethnicity
L B Feuchtbaum, R J Currier, S Riggle, et al.
Genetic Testing
|
September 25, 1999
Mutations in exon 3 of the PAH gene causing mild hyperphenylalaninemia
C Zekanowski, M Nowacka, M Gizewska, et al.
Genetic Testing
|
May 4, 2000
P53 mutations, polymorphisms, and haplotypes in Pakistani ethnic groups and breast cancer patients
S Khaliq, A Hameed, T Khaliq, et al.
Genetic Testing
|
May 4, 2000
Molecular analysis in Brazilian cystic fibrosis patients reveals five novel mutations
A L Bernardino, A Ferri, M R Passos-Bueno, et al.
Genetic Testing
|
August 23, 2000
Postscript: a status report on hemochromatosis population screening
F Gilbert
Genetic Testing
|
January 15, 2002
Psychological aspects of genetic counseling. XIV. Nondirectiveness and counseling skills
S Kessler
Page
of 68