Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Deborah E. Kaplan"'
Autor:
Deborah E. Kaplan
Publikováno v:
Pedagogy. 18:87-107
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::364727db4baaeb1dd0b84088013b406c
https://doi.org/10.1215/15314200-4216962
https://doi.org/10.1215/15314200-4216962
Autor:
Melanie K Finney, Heather Slawecki, Nancy H Womack, Kathleen Fordyce, Ellen Schrecker, Joan Gussow, Christine Silverstein, Michele Neff Hernandez, Roni Sherman Ramos, Deborah E Kaplan, Lise Menn, Maggie Madagame, Barbara Marwell, Edie Butler, Raquel Ramkhelawan, Kelli Dunham, Mimi Schwartz, P.C. Moorehead, Joan Michelson, Susanne Braham, Alice Derry, Alice Radosh, Alice Goode-Elman, Parvin Hajizadeh, Patricia Life, Lauren Vanett, Sonia Jaffe Robbins, Maxine Marshall, Molly A McEneny, Nancy Shamban, Doris Friedensohn, Merle Froschl, Andrea Hirshman, Debby Mayer, Anne Bernays, Elisa Clark Wadham, Tracy Milcendeau, Penelope Dugan, Kathryn Temple, Tara Sabharwal, Jean Y Leung, Carrie L West
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f1e1288326dce0ee6b564b3fc450db32
https://doi.org/10.36019/9780813599571
https://doi.org/10.36019/9780813599571
Autor:
Joel Gelernter, Jung Ahn, Tae-Woong Won, Eric Londin, Deborah E. Kaplan, Jeffrey R. Gruen, Petr Kuzmic
Publikováno v:
Human Genetics. 111:339-349
Loci for several complex disorders have been genetically linked to markers located telomeric of the HLA class I region of the major histocompatibility complex on 6p21.3-22. However, this same region has been characterized by a large interval of recom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19758b35f7505a1e6eb25b45be2ffc0d
https://doi.org/10.1007/s00439-002-0771-x
https://doi.org/10.1007/s00439-002-0771-x
Autor:
Richard K. Olson, Javier Gayán, Bruce F. Pennington, Frank B. Wood, Tae-Woong Won, Jung Ahn, Deborah E. Kaplan, David L. Pauls, Jeffrey R. Gruen, John C. DeFries, Grier P. Page, Shelley D. Smith
Publikováno v:
The American Journal of Human Genetics. 70:1287-1298
Reading disability (RD), or dyslexia, is a common heterogeneous syndrome with a large genetic component. Several studies have consistently found evidence for a quantitative-trait locus (QTL) within the 17 Mb (14.9 cM) that span D6S109 and D6S291 on c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce570dc546ee6d9c077c946c20a574e8
https://doi.org/10.1086/340449
https://doi.org/10.1086/340449
Publikováno v:
PM&R. 3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::25546763ca639994971f4b7e190d6d07
https://doi.org/10.1016/j.pmrj.2011.08.486
https://doi.org/10.1016/j.pmrj.2011.08.486