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	Title	Author(s)	Issue Date
	Analysis of the human Sonic Hedgehog coding and promoter regions in sacral agenesis, triphalangeal thumb, and mirror polydactyly Journal:Human Genetics	Vargas, FR Roessler, E Gaudenz, K Belloni, E Whitehead, AS Kirke, PN Mills, JL Hooper, G Stevenson, RE Cordeiro, I Correia, P Felix, T Gereige, R Cunningham, ML Canún, S Antonarakis, SE Strachan, T Tsui, LC Scherer, SW Muenke, M	1998
	Chromosomal localization in mouse and human of the vasoactive intestinal peptide receptor type 2 gene: A possible contributor to the holoprosencephaly 3 phenotype Journal:Genomics	Mackay, M Fantes, J Scherer, S Boyle, S West, K Tsui, LC Belloni, E Lutz, E Van Heyningen, V Harmar, AJ	1996
	Cytogenetic rearrangements involving the loss of the Sonic Hedgehog gene at 7q36 cause holoprosencephaly Journal:Human Genetics	Roessler, E Ward, DE Gaudenz, K Belloni, E Scherer, SW Donnai, D SiegelBartelt, J Tsui, LC Muenke, M	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 Sonic hedgehog as a candidate gene responsible for holoprosencephaly. Journal:Nature genetics	Belloni, E Muenke, M Roessler, E Traverso, G SiegelBartelt, J Frumkin, A Mitchell, HF DonisKeller, H Helms, C Hing, AV Heng, HH Koop, B Martindale, D Rommens, JM Tsui, LC Scherer, SW	1996
	Involvement of the HLXB9 homeobox gene in Currarino syndrome [2] Journal:American Journal of Human Genetics	Belloni, E Martucciello, G Verderio, D Ponti, E Seri, M Jasonni, V Torre, M Ferrari, M Tsui, LC Scherer, SW	2000
	Localization of two metabotropic glutamate receptor genes, GRM3 and GRM8, to human chromosome 7q Journal:Genomics	Scherer, SW Duvoisin, RM Kuhn, R Heng, HHQ Belloni, E Tsui, LC	1996
	Mutations in the C-terminal domain of Sonic Hedgehog cause holoprosencephaly Journal:Human Molecular Genetics	Roessler, E Belloni, E Gaudenz, K Vargas, F Scherer, SW Tsui, LC Muenke, M	1997
	Mutations in the human Sonic Hedgehog gene cause holoprosencephaly. Journal:Nature genetics	Roessler, E Belloni, E Gaudenz, K Jay, P Berta, P Scherer, SW Tsui, LC Muenke, M	1996
	Physical mapping of the split hand/split foot locus on chromosome 7 and implication in syndromic ectrodactyly Journal:Human Molecular Genetics	Scherer, SW Poorkaj, P Massa, H Soder, S Allen, T Nunes, M Geshuri, D Wong, E Belloni, E Little, S Zhou, L Becker, D Kere, J Ignatius, J Niikawa, N Fukushima, Y Hasegawa, T Weissenbach, J Boncinelli, E Trask, B Tsui, L-C Evans, JP	1994
	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 11 of 11