Zobrazeno 1 - 10
of 1 254
pro vyhledávání: '"Voullaire, L."'
Autor:
Howden, S. E.1,2,3 s.howden@pgrad.unimelb.edu.au, Voullaire, L.1, Wardan, H.1, Williamson, R.2,3, Vadolas, J.1
Publikováno v:
Gene Therapy. Oct2008, Vol. 15 Issue 20, p1372-1383. 12p. 1 Color Photograph, 1 Black and White Photograph, 2 Diagrams, 1 Chart, 3 Graphs.
Autor:
Xie, Mengzhen1,2 (AUTHOR), Wang, Lixiang1 (AUTHOR), Deng, Yingping1 (AUTHOR), Ma, Ke1 (AUTHOR), Yin, Hongbo1 (AUTHOR), Zhang, Xiaolan1 (AUTHOR), Xiang, Xingye3,4 (AUTHOR), Tang, Jing1 (AUTHOR) tangjing0802@163.com, Zhou, Yedi (AUTHOR)
Publikováno v:
Journal of Ophthalmology. 9/9/2024, Vol. 2024, p1-14. 14p.
Publikováno v:
Journal of Gene Medicine; Jan2008, Vol. 10 Issue 1, p42-50, 9p
Autor:
Meza-Espinoza, Juan Pablo1 (AUTHOR), González-García, Juan Ramón2 (AUTHOR), Nieto-Marín, Nayeli3 (AUTHOR), Patrón-Baro, Liliana Itzel3 (AUTHOR), González-Arreola, Rosa María4 (AUTHOR), Arámbula-Meraz, Eliakym5 (AUTHOR), Benítez-Pascual, Julio6 (AUTHOR), De la Herrán-Arita, Alberto Kousuke7 (AUTHOR), Norzagaray-Valenzuela, Claudia Desireé8 (AUTHOR), Valdez-Flores, Marco Antonio7 (AUTHOR), Carrillo-Cázares, Tomás Adrián7 (AUTHOR), Picos-Cárdenas, Verónica Judith7 (AUTHOR) veronicapicos@uas.edu.mx
Publikováno v:
Molecular Cytogenetics (17558166). 7/18/2024, Vol. 17 Issue 1, p1-9. 9p.
Publikováno v:
Molecular Human Reproduction; Nov2002, Vol. 8 Issue 11, p1035-1041, 7p
Autor:
Penny, L. A., Aquila, M., Jones, M. C., Bergoffen, J., Cunniff, C., Fryns -, J. P., Grace, E., Graham Jr, J. M., Kousseff, B., Teresa Mattina, Syme, J., Voullaire, L., Zelante, L., Zenger-Hain, J., Jones, O. W., Evans, G. A.
Publikováno v:
Scopus-Elsevier
Jacobsen syndrome is caused by segmental aneusomy for the distal end of the long arm of chromosome 11. Typical features include mild to moderate psychomotor retardation, trigonocephaly, facial dysmorphism, cardiac defects, and thrombocytopenia, thoug
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::547c68466061652f14bdf0bb357c5cc0
https://europepmc.org/articles/PMC1801184/
https://europepmc.org/articles/PMC1801184/
We report the investigation of an unusual human supernumerary marker chromosome 10 designated "mar del(10)." This marker is present together with two other marker chromosomes in the karyotype of a boy with mild developmental delay. It has a functiona
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6ca8ecd31f6dde16d375f8063acd12de
https://europepmc.org/articles/PMC1682274/
https://europepmc.org/articles/PMC1682274/
Autor:
De Leo, A., Guedelha, N., Toder, R., Voullaire, L., Ferguson-Smith, M., O'Brien, P., Graves, J.
Publikováno v:
Chromosome Research; Dec1999, Vol. 7 Issue 7, p509-517, 9p
Autor:
Hills, L., Earle, E., Wilson, M., Petrovic, V., Voullaire, L., Leversha, M., Danks, D., Choo, K.
Publikováno v:
Human Genetics; 1991, Vol. 87 Issue 2, p173-176, 4p
Akademický článek
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