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Showing results 1 to 11 of 11

	Title	Author(s)	Issue Date
	A 1.5 million-base pair inversion polymorphism in families with Williams-Beuren syndrome Journal:Nature Genetics	Osborne, LR Li, M Pober, B Chitayat, D Bodurtha, J Mandel, A Costa, T Grebe, T Cox, S Tsui, LC Scherer, SW	2001
	Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia Journal:American Journal of Human Genetics	Feuk, L Kalervo, A LipsanenNyman, M Skaug, J Nakabayashi, K Finucane, B Hartung, D Innes, M Kerem, B Nowaczyk, MJ Rivlin, J Roberts, W Senman, L Summers, A Szatmari, P Wong, V Vincent, JB Zeesman, S Osborne, LR Cardy, JO Kere, J Scherer, SW HannulaJouppi, K	2006
	Assignment of the human CC chemokine MPIF-2/eotaxin-2 (SCYA24) to chromosome 7q11.23 Journal:Genomics	Nomiyama, H Osborne, LR Imai, T Kusuda, J Miura, R Tsui, LC Yoshie, O	1998
	The BCL7 gene family: Deletion of BCL7B in Williams syndrome Journal:Gene	Jadayel, DM Osborne, LR Coignet, LJA Zani, VJ Tsui, LC Scherer, SW Dyer, MJS	1998
	Hemizygous deletion of the syntaxin 1A gene in individuals with Williams syndrome: Letters to the editor	Osborne, LR Soder, S Shi, XM Pober, B Costa, T Scherer, SW Tsui, L-C	1997
	Human chromosome 7: DNA sequence and biology Journal:Science	Scherer, SW Cheung, J MacDonald, JR Osborne, LR Nakabayashi, K Herbrick, JA Carson, AR ParkerKatiraee, L Skaug, J Khaja, R Zhang, J Hudek, AK Li, M Haddad, M Duggan, GE Fernandez, BA Kanematsu, E Gentles, S Christopoulos, CC Choufani, S Kwasnicka, D Zheng, XH Lai, Z Nusskern, D Zhang, Q Gu, Z Lu, F Zeesman, S Nowaczyk, MJ Teshima, I Chitayat, D Shuman, C Weksberg, R Zackai, EH Grebe, TA Cox, SR Kirkpatrick, SJ Rahman, N Friedman, JM Heng, HHQ Pelicci, PG LoCoco, F Belloni, E Shaffer, LG Pober, B Morton, CC Gusella, JF Bruns, GAP Korf, BR Quade, BJ Ligon, AH Ferguson, H Higgins, AW Leach, NT Herrick, SR Lemyre, E Farra, CG Kim, HG Summers, AM Gripp, KW Roberts, W Szatmari, P Winsor, EJT Grzeschik, KH Teebi, A Minassian, BA Kere, J Armengol, L Pujana, MA Estivill, X Wilson, MD Koop, BF Tosi, S Moore, GE Boright, AP Zlotorynski, E Kerem, B Kroisel, PM Petek, E Oscier, DG Mould, SJ Döhner, H Döhner, K Rommens, JM Vincent, JB Venter, JC Li, PW Mural, RJ Adams, MD Tsui, LC	2003
	Identification of a putative transcription factor gene (WBSCR11) that is commonly deleted in Williams-Beuren syndrome Journal:Genomics	Osborne, LR Campbell, T Daradich, A Scherer, SW Tsui, LC	1999
	Identification of genes from a 500-kb region at 7q11.23 that is commonly deleted in Williams syndrome patients Journal:Genomics	Osborne, LR Martindale, D Scherer, SW Shi, XM Huizenga, J Heng, HHQ Costa, T Pober, B Lew, L Brinkman, J Rommens, J Koop, B Tsui, LC	1996
	Influence of restraint stress on the expression and the serine/threonine phosphatase activity of calcineurin in the rat brain Journal:Synapse	Wu, YQ Bejjani, BA Tsui, LC Mandel, A Osborne, LR Shaffer, LG	2001
	PMS2-related genes flank the rearrangement breakpoints associated with Williams syndrome and other diseases on human chromosome 7 Journal:Genomics	Osborne, LR Herbrick, JA Greavette, T Heng, HHQ Tsui, LC Scherer, SW	1997
	Refinement of the genomic structure of STX1A and mutation analysis in nondeletion Williams syndrome patients Journal:American Journal of Medical Genetics	Wu, YQ Bejjani, BA Tsui, LC Mandel, A Osborne, LR Shaffer, LG	2002

Showing results 1 to 11 of 11