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Genetic Testing and Molecular Biomarkers|April 8, 2022
Improved HUMARA for the Detection of X-Linked Agammaglobulinemia CarriersEduardo Carrillo-Tapia, Sara E Espinosa-Padilla, Daniela Perez-Perez, et al.Genetic Testing and Molecular Biomarkers|September 21, 2018
Genetic and Functional Analyses of Two Missense Mutations in the Transcription Factor FOXL2 in Two Chinese Families with Blepharophimosis-Ptosis-Epicanthus Inversus SyndromeHuiyan Li, Yangshun GuGenetic Testing and Molecular Biomarkers|July 21, 2010
FMR1 protein expression in blood smears for fragile X syndrome diagnosis in a Mexican population samplePavel Romero-Espinoza, Mónica A Rosales-Reynoso, Rob Willemsen, et al.Genetic Testing and Molecular Biomarkers|July 21, 2010
Risk of myocardial infarction related to factor V Leiden mutation: a meta-analysisMoataz Dowaidar, Ahmad SettinGenetic Testing and Molecular Biomarkers|July 21, 2010
Recurrent and private MYO15A mutations are associated with deafness in the Turkish populationF Basak Cengiz, Duygu Duman, Asli Sirmaci, et al.Genetic Testing and Molecular Biomarkers|July 21, 2010
The ethnospecific distribution of the HFE haplotypes for IVS2(+4)t/c, IVS4(-44)t/c, and IVS5(-47)g/a in populations of Russia and possible effects of these single-nucleotide polymorphisms in splicingSvetlana Vladimirovna Mikhailova, Vladimir Nikolaevich Babenko, Mikhail Ivanovich Voevoda, et al.Genetic Testing and Molecular Biomarkers|October 29, 2010
Population structure of Aggarwals of north India as revealed by molecular markersVipin Gupta, Rajesh Khadgawat, Hon Keung Tony Ng, et al.Genetic Testing and Molecular Biomarkers|October 29, 2010
Health-care referrals from direct-to-consumer genetic testingMonica A Giovanni, Matthew R Fickie, Lisa S Lehmann, et al.Genetic Testing and Molecular Biomarkers|October 29, 2010
Hereditary hemochromatosis: awareness and genetic testing acceptability in Western RomaniaAdriana Maria Neghina, Andrei AnghelGenetic Testing and Molecular Biomarkers|September 30, 2010
GATA4 mutations in 357 unrelated patients with congenital heart malformationTanya L Butler, Giorgia Esposito, Gillian M Blue, et al.Pageof 193