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	Title	Author(s)	Issue Date	Views
	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	106
	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	217
	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	172
	Mutational spectrum of the oral-facial-digital type I syndrome: A study on a large collection of patients Journal:Human Mutation	Prattichizzo, C Macca, M Novelli, V Giorgio, G Barra, A Franco, B Abdulla, F Abramowicz, M Amy, S Schafer, I Bankier, A White, S Barcina, MG Bartoshesky, LE Jenny, K Beemer, FA Benke, P Betz, RC Bianchini, G Garavelli, L Bigoni, S Bird, L Chibuk, J MasserFrye, D Brunetti, N Scarcella, A Brunner, HG Burn, J Carmi, R Castellan, C Castelluccio, P Castle, B Chiong, MA Cutiongco, EM Collins, F Couchon, E Curry, A Pastore, M Curry, C Swenerton, A Treisman, T Dean, J Devriendt, K Matthijs, G Dunlap, JW Shashi, V Elcioglu, N Farndon, P Ferrero, GB Ferrier, R Foulds, N Friedman, JM Gal, A Orth, U Gardner, M Gerola, O GillessenKaesbach, G Giuliano, F TurcCarel, C Gödde, E Graber, V Graham, GE Gurrieri, F Harbour, L Henderson, A Jones, E Heran, H Homfray, T Taylor, R Iwarsson, E Jensen, P JezelaStanek, A Joss, S Taylor, G Keeling, SL Klatt, R Teebi, A KlehrMartinelli, M Kotzot, D Lees, M Loughlin, S Lhotta, K Macdonald, F Mari, F Renieri, A Marlin, S Mcgaughran, J Mckenzie, F Mcleod, DR Megarbane, A Mota, CR Mucke, J Tzschach, A Obersztyn, E Okhowat, R Shinzel, A Pfau, R Pober, B Raymond, FL Reich, E Reimschisel, T Robertson, J Roggenbuck, J Sabato, A Sanchez Del Pozo, J SchellApacik, C Schwaab, E Selicorni, A Sell, S Smithson, S StrayPedersen, A Tan, T Thiese, H Tol, J Toprak, O Trump, D Whittaker, J Williams, D Zelante, L Zoll, B	2008	78
	Tourette syndrome in two brothers with balanced and unbalanced chromosome 12 rearrangements	Yu, J Guan, X Pober, B Yang-Feng, T	1999	104

Showing results 2 to 6 of 6 < previous