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Genetic testing

Showing results (401-410 of 679) with videos related to

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Genetic Testing|December 29, 2005
Gene sequencing in neonates and infants with the long QT syndromeSung Han Shim, Masamichi Ito, Thomas Maher, et al.
Genetic Testing|December 29, 2005
Indirect CFTR mutation identification by PCR/OLA anomalous electropherogramsPietro Stanziale, Maria Savino, Patrizia De Bonis, et al.
Genetic Testing|December 29, 2005
The effect of preventability and severity levels of a genetic disorder on desire to communicate genetic testing information to family membersJennifer A Crabb, Diane C Tucker, Eun Young Mun
Genetic Testing|October 18, 2005
Identification of novel cystinuria mutations and polymorphisms in SLC3A1 and SLC7A9 genes: absence of SLC7A10 gene mutations in cystinuric patientsAnthoula Chatzikyriakidou, Nikolaos Sofikitis, Ioannis Georgiou
Genetic Testing|October 18, 2005
Constitutional and somatic RB1 mutation spectrum in nonfamilial unilateral and bilateral retinoblastoma in IndiaM N Bamne, P N Ghule, J Jose, et al.
Genetic Testing|October 18, 2005
Arrayed primer extension: a robust and reliable genotyping platform for the diagnosis of single gene disorders: beta-thalassemia and thiopurine methyltransferase deficiencyYi Lu, Shirley Kow-Yin Kham, Poh-Lin Tan, et al.
Genetic Testing|December 4, 2003
Denaturing high-performance liquid chromatography quickly and reliably detects cardiac ion channel mutations in long QT syndromeLi Ning, Arthur Moss, Woject Zareba, et al.
Genetic Testing|October 24, 2007
Severe MDC1A congenital muscular dystrophy due to a splicing mutation in the LAMA2 gene resulting in exon skipping and significant decrease of mRNA levelOlfa Siala, Nacim Louhichi, Chahnez Triki, et al.
Genetic Testing|October 24, 2007
Screening for Alagille syndrome mutations in the JAG1 and NOTCH2 genes using denaturing high-performance liquid chromatographyHazuki Samejima, Chiharu Torii, Rika Kosaki, et al.
Genetic Testing|October 24, 2007
HFE C282Y homozygotes aged 25-29 years at HEIRS Study initial screeningJames C Barton, Ronald T Acton, Catherine Leiendecker-Foster, et al.
Pageof 68

Showing results (401-410 of 679) with videos related to

Sort By:
Pageof 68
Genetic Testing|December 29, 2005
Gene sequencing in neonates and infants with the long QT syndromeSung Han Shim, Masamichi Ito, Thomas Maher, et al.
Genetic Testing|December 29, 2005
Indirect CFTR mutation identification by PCR/OLA anomalous electropherogramsPietro Stanziale, Maria Savino, Patrizia De Bonis, et al.
Genetic Testing|December 29, 2005
The effect of preventability and severity levels of a genetic disorder on desire to communicate genetic testing information to family membersJennifer A Crabb, Diane C Tucker, Eun Young Mun
Genetic Testing|October 18, 2005
Identification of novel cystinuria mutations and polymorphisms in SLC3A1 and SLC7A9 genes: absence of SLC7A10 gene mutations in cystinuric patientsAnthoula Chatzikyriakidou, Nikolaos Sofikitis, Ioannis Georgiou
Genetic Testing|October 18, 2005
Constitutional and somatic RB1 mutation spectrum in nonfamilial unilateral and bilateral retinoblastoma in IndiaM N Bamne, P N Ghule, J Jose, et al.
Genetic Testing|October 18, 2005
Arrayed primer extension: a robust and reliable genotyping platform for the diagnosis of single gene disorders: beta-thalassemia and thiopurine methyltransferase deficiencyYi Lu, Shirley Kow-Yin Kham, Poh-Lin Tan, et al.
Genetic Testing|December 4, 2003
Denaturing high-performance liquid chromatography quickly and reliably detects cardiac ion channel mutations in long QT syndromeLi Ning, Arthur Moss, Woject Zareba, et al.
Genetic Testing|October 24, 2007
Severe MDC1A congenital muscular dystrophy due to a splicing mutation in the LAMA2 gene resulting in exon skipping and significant decrease of mRNA levelOlfa Siala, Nacim Louhichi, Chahnez Triki, et al.
Genetic Testing|October 24, 2007
Screening for Alagille syndrome mutations in the JAG1 and NOTCH2 genes using denaturing high-performance liquid chromatographyHazuki Samejima, Chiharu Torii, Rika Kosaki, et al.
Genetic Testing|October 24, 2007
HFE C282Y homozygotes aged 25-29 years at HEIRS Study initial screeningJames C Barton, Ronald T Acton, Catherine Leiendecker-Foster, et al.
Pageof 68