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Showing results 1 to 8 of 8

	Title	Author(s)	Issue Date
	Assignment of the SLC25A12 gene coding for the human calcium-binding mitochondrial solute carrier protein aralar to human chromosome 2q24 Journal:Cytogenetics and Cell Genetics	Crackower, MA Sinasac, DS Lee, JR Herbrick, JA Tsui, LC Scherer, SW	1999
	Fusion of two novel genes, RBM15 and MKL1, in the t(1;22)(p13;q13) of acute megakaryoblastic leukemia Journal:Nature Genetics	Ma, Z Morris, SW Valentine, V L, M Herbrick, JA Cui, X Bouman, D Li, Y Mehta, PK Nizetic, D Kaneko, Y Chan, GCF Chan, LC Squire, J Scherer, SW Hitzler, JK	2001
	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
	Mapping of the human Lunatic Fringe (LFNG) gene to 7p22 and Manic Fringe (MFNG) to 22q12 Journal:Genomics	Egan, S Herbrick, JA Tsui, LC Cohen, B Flock, G Beatty, B Scherer, SW	1998
	Molecular analysis of the PDS gene in Pendred syndrome (sensorineural hearing loss and goitre) Journal:Human Molecular Genetics	Coyle, B Reardon, W Herbrick, JA Tsui, LC Gausden, E Lee, J Coffey, R Grueters, A Grossman, A Phelps, PD Luxon, L KendallTaylor, P Scherer, SW Trembath, RC	1998
	Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsy Journal:Nature Genetics	Minassian, BA Lee Jeffrey, R Herbrick, JA Huizenga, J Soder, S Mungall, AJ Dunham, I Gardner, R Fong, CYG Carpenter, S Jardim, L Satishchandra, P Andermann, E Carter Snead III, O LopesCendes, I Tsui, LC DelgadoEscueta, AV Rouleau, GA Scherer, SW	1998
	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
	Population differences in the polyalanine domain and 6 new mutations in HLXB9 in patients with Currarino syndrome Journal:Clinical Chemistry	GarciaBarceló, M So, MT Lau, DKC Leon, TYY Yuan, ZW Cai, WS Lui, VCH Fu, M Herbrick, JA Gutter, E Proud, V Li, L PierreLouis, J Aleck, K Van Heurn, E Belloni, E Scherer, SW Tam, PKH	2006

Showing results 1 to 8 of 8