Zobrazeno 1 - 4
of 4
pro vyhledávání: '"L O, Maddox"'
Autor:
G. R. DeLong, Andrew W. Zimmerman, M. M. Menold, Meredyth P. Bass, J. M. Vance, Harry H. Wright, Eden R. Martin, Sarah A. Ravan, Margaret A. Pericak-Vance, John R. Gilbert, Ruth K. Abramson, Michael L. Cuccaro, Chantelle M. Wolpert, S. L. Donnelly, L. O. Maddox
Publikováno v:
American Journal of Medical Genetics. 96:43-48
Autistic disorder (AD) is a neurodevelopmental disorder characterized by abnormalities in behavior, communication, and social interactions and functioning. Recently, Cook et al. reported significant linkage disequilibrium with an AD susceptibility lo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e53b5ccd2c12e2de839a1e649f6cfe77
https://doi.org/10.1002/(sici)1096-8628(20000207)96:1<43::aid-ajmg9>3.0.co
https://doi.org/10.1002/(sici)1096-8628(20000207)96:1<43::aid-ajmg9>3.0.co
Autor:
Jeffery M. Vance, G. R. DeLong, Michael L. Cuccaro, Elizabeth R. Hauser, L. O. Maddox, Sarah A. Ravan, Ruth K. Abramson, Chantelle M. Wolpert, M. M. Menold, Harry H. Wright, John R. Gilbert, Margaret A. Pericak-Vance, Meredyth P. Bass, S. L. Donnelly
Publikováno v:
Neurogenetics. 2(4)
Autistic disorder (AD) is a developmental disorder affecting social interactions, communication, and behavior. AD is a disease of complex genetic architecture. It is postulated that several genes contribute to the underlying etiology of AD. Chromosom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8ca1dba20e1c3e0ee1723688655afb3
https://pubmed.ncbi.nlm.nih.gov/10983717
https://pubmed.ncbi.nlm.nih.gov/10983717
Autor:
E R, Martin, M M, Menold, C M, Wolpert, M P, Bass, S L, Donnelly, S A, Ravan, A, Zimmerman, J R, Gilbert, J M, Vance, L O, Maddox, H H, Wright, R K, Abramson, G R, DeLong, M L, Cuccaro, M A, Pericak-Vance
Publikováno v:
American journal of medical genetics. 96(1)
Autistic disorder (AD) is a neurodevelopmental disorder characterized by abnormalities in behavior, communication, and social interactions and functioning. Recently, Cook et al. reported significant linkage disequilibrium with an AD susceptibility lo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f0bd677ef1c135d5151ddd73e215a0c7
https://pubmed.ncbi.nlm.nih.gov/10686550
https://pubmed.ncbi.nlm.nih.gov/10686550
Autor:
Maria Descartes, Andrew J. Carroll, Ruben Kuzniecky, S Rosenfeld, J M Keating, J Collins, L. O. Maddox, Cheryl A. Palmer
Publikováno v:
Scopus-Elsevier
Patients affected with progressive myoclonus epilepsy of the Lafora type present during late adolescence with a characteristic EEG pattern and Lafora bodies seen on skin biopsy. The critical region for the Lafora gene has been localised to chromosome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70f9a3fb7a022deb86c1f143a2bbf745
https://doi.org/10.1136/jmg.34.7.590
https://doi.org/10.1136/jmg.34.7.590