Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Tina Sellers"'
Autor:
Claudia Grauf-Grounds, Tina Sellers, Scott A. Edwards, Hee-Sun Cheon, Don Macdonald, Shawn Whitney, Peter Rivera
A Practice Beyond Cultural Humility offers specific guidance to support students and practitioners in providing on-going, culturally-attuned professional care. The book introduces a multicultural diversity-training model named the ORCA-Stance, an int
Autor:
Louis Geller, Arlene Buller, Jean Amos Wilson, William Edward Highsmith, Kasinathan Muralidharan, Tina Sellers, Ruth Kornreich, Elizabeth M. Rohlfs, Toby L. Payeur, Lisa Edelmann, Leonard M. Holtegaard, Lisa V. Kalman, Lorraine Toji, John Dixon
Publikováno v:
The Journal of Molecular Diagnostics. 11:530-536
Many recessive genetic disorders are found at a higher incidence in people of Ashkenazi Jewish (AJ) descent than in the general population. The American College of Medical Genetics and the American College of Obstetricians and Gynecologists have reco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::862935cd4ebe80eb8346981f2c59dfa9
https://doi.org/10.2353/jmoldx.2009.090050
https://doi.org/10.2353/jmoldx.2009.090050
Autor:
Samantha Maragh, Monique A. Johnson, Elizabeth Berry-Kravis, Kristy L. Richie, Kasinathan Muralidharan, Frederick V. Schaefer, Tina Sellers, Lisa V. Kalman, Karla J. Matteson, Elaine B. Spector, James H. Handsfield, Brett Casey, Jeanne C. Beck, Elizabeth M. Rohlfs, Arlene Buller, Gerald L. Feldman, C. Sue Richards, John P. Jakupciak
Publikováno v:
Genetics in Medicine. 9:719-723
Purpose: Diagnostic and predictive testing for Huntington disease requires an accurate measurement of CAG repeats in the HD (IT15) gene. However, precise repeat sizing can be technically challenging, and is complicated by the lack of quality control
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a77958b5ffaf2cfb52c34ce0e5fff2d
https://doi.org/10.1097/gim.0b013e318156e8c1
https://doi.org/10.1097/gim.0b013e318156e8c1
Autor:
Lidia Epp, Lawrence M. Silverman, Victoria M. Pratt, Jean Amos Wilson, C. Sue Richards, Kasinathan Muralidharan, Scott J. Bridgeman, W. Edward Highsmith, Ebony M. Courtney, Amit Phansalkar, Jeanne C. Beck, John P. Jakupciak, Leonard M. Holtegaard, Monique A. Johnson, Paul Labrousse, Nick L. Hjelm, Elaine Lyon, Andrea Ferreira-Gonzalez, Thomas W. Prior, Joanna Wiszniewska, Kristy L. Richie, Elizabeth M. Rohlfs, Karen A. Siegrist, Lisa V. Kalman, Tina Sellers, Benjamin B. Roa, Mohamed Jama, Stephanie L. Sherman
Publikováno v:
The Journal of molecular diagnostics : JMD. 10(1)
Fragile X syndrome, which is caused by expansion of a (CGG)(n) repeat in the FMR1 gene, occurs in approximately 1:3500 males and causes mental retardation/behavioral problems. Smaller (CGG)(n) repeat expansions in FMR1, premutations, are associated w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8ce9c28264e48ac26ee526c2808ea04
https://pubmed.ncbi.nlm.nih.gov/18165276
https://pubmed.ncbi.nlm.nih.gov/18165276