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Genetic testing

Showing results (391-400 of 679) with videos related to

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Genetic Testing|January 1, 1997
Fine mapping of the human 5-HTR2a gene to chromosome 13q14 and identification of two highly polymorphic linked markers suitable for association studies in psychiatric disordersD A Campbell, D Sundaramurthy, A F Markham, et al.
Genetic Testing|August 28, 1999
Mutations in the SLC3A1 gene in cystinuric patients: frequencies and identification of a novel mutationA Albers, S Lahme, C Wagner, et al.
Genetic Testing|August 28, 1999
HER-2/neu oncogene amplification in cervical cancer studied by fluorescent in situ hybridizationH F Mark, D Feldman, S Das, et al.
Genetic Testing|January 11, 2000
Genetic testing for early-onset torsion dystonia (DYT1): introduction of a simple screening method, experiences from testing of a large patient cohort, and ethical aspectsC Klein, J Friedman, S Bressman, et al.
Genetic Testing|January 11, 2000
Inherited thrombophilia genes in minoritiesR Mack, D Chowdary, D Streck, et al.
Genetic Testing|January 11, 2000
Disease genes and chromosomes: disease maps of the human genome. Chromosome 14F Gilbert
Genetic Testing|August 30, 2008
Prenatal diagnosis of spinal muscular atrophy in Macedonian familiesSvetlana A Kocheva, Dijana Plaseska-Karanfilska, Svetlana Trivodalieva, et al.
Genetic Testing|August 30, 2008
BRCA1/2 in high-risk African American women with breast cancer: providing genetic testing through various recruitment strategiesTuya Pal, Susan Vadaparampil, Judy Betts, et al.
Genetic Testing|December 17, 2008
A known SOST gene mutation causes sclerosteosis in a familial and an isolated case from Brazilian originChong Ae Kim, Rachel Honjo, Débora Bertola, et al.
Genetic Testing|December 17, 2008
A novel frameshift mutation in FRMD7 causing X-linked idiopathic congenital nystagmusXiang He, Feng Gu, Ze Wang, et al.
Pageof 68

Showing results (391-400 of 679) with videos related to

Sort By:
Pageof 68
Genetic Testing|January 1, 1997
Fine mapping of the human 5-HTR2a gene to chromosome 13q14 and identification of two highly polymorphic linked markers suitable for association studies in psychiatric disordersD A Campbell, D Sundaramurthy, A F Markham, et al.
Genetic Testing|August 28, 1999
Mutations in the SLC3A1 gene in cystinuric patients: frequencies and identification of a novel mutationA Albers, S Lahme, C Wagner, et al.
Genetic Testing|August 28, 1999
HER-2/neu oncogene amplification in cervical cancer studied by fluorescent in situ hybridizationH F Mark, D Feldman, S Das, et al.
Genetic Testing|January 11, 2000
Genetic testing for early-onset torsion dystonia (DYT1): introduction of a simple screening method, experiences from testing of a large patient cohort, and ethical aspectsC Klein, J Friedman, S Bressman, et al.
Genetic Testing|January 11, 2000
Inherited thrombophilia genes in minoritiesR Mack, D Chowdary, D Streck, et al.
Genetic Testing|January 11, 2000
Disease genes and chromosomes: disease maps of the human genome. Chromosome 14F Gilbert
Genetic Testing|August 30, 2008
Prenatal diagnosis of spinal muscular atrophy in Macedonian familiesSvetlana A Kocheva, Dijana Plaseska-Karanfilska, Svetlana Trivodalieva, et al.
Genetic Testing|August 30, 2008
BRCA1/2 in high-risk African American women with breast cancer: providing genetic testing through various recruitment strategiesTuya Pal, Susan Vadaparampil, Judy Betts, et al.
Genetic Testing|December 17, 2008
A known SOST gene mutation causes sclerosteosis in a familial and an isolated case from Brazilian originChong Ae Kim, Rachel Honjo, Débora Bertola, et al.
Genetic Testing|December 17, 2008
A novel frameshift mutation in FRMD7 causing X-linked idiopathic congenital nystagmusXiang He, Feng Gu, Ze Wang, et al.
Pageof 68