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Showing results 94 to 110 of 110 < previous

	Title	Author(s)	Issue Date
	Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder Journal:Nature Neuroscience	Lim, ET Uddin, M De Rubeis, S Chan, Y Kamumbu, AS Zhang, X D'Gama, AM Kim, SN Hill, RS Gikdberg, AP Poultney, C Minshew, NJ Kushima, I Aleksic, B Ozaki, N Parellada, M Arango, C Penzol, MJ Carracedo, A Kolevzon, A Hultman, CM Weiss, LA Fromer, M Chiocchetti, AG Freitag, CM Church, GM Scherer, SW Buxbaum, JD Walsh, CA Autism Sequencing Consortium Chung, BHY	2017
	Refined localization and yeast artificial chromosome (YAC) contig-mapping of genes and DNA segments in the 7q21-q32 region Journal:Human Molecular Genetics	Scherer, SW Rommens, JM Soder, S Wong, E Plavsic, N Tompkins, BJF Beattie, A Kim, J Tsui, LC	1993
	Refined localization of the asparagine synthetase gene (ASNS) to chromosome 7, region q21.3, and characterization of the somatic cell hybrid line 4AF/106/K015 Journal:Cytogenetics and Cell Genetics	Heng, HHQ Shi, XM Scherer, SW Andrulis, IL Tsui, LC	1994
	Regional localization of 725 human chromosome 7-specific yeast artificial chromosome clones Journal:Genomics	Kunz, J Scherer, SW Klawitz, I Soder, S Du, YZ Speich, N KalffSuske, M Heng, HHQ Tsui, LC Grzeschik, KH	1994
	Regional localization of the CCAAT displacement protein gene (CUTL1) to 7q22 by analysis of somatic cell hybrids Journal:Genomics	Scherer, SW Neufeld, EJ Lievens, MJ Orkin, SH Kim, J Tsui, LC	1993
	Replication delay along FRA7H, a common fragile site on human chromosome 7, leads to chromosomal instability Journal:Molecular and Cellular Biology	Hellman, A Rahat, A Scherer, SW Darvasi, A Tsui, LC Kerem, B	2000
	Role of epigenetic dysregulation in neurodevelopmental syndromes: lessons from KDM5C mutations Proceeding/Conference:ICHG-ASHG 2011 Joint Meeting	Grafodatskaya, D Chung, BHY Butcher, DT Goodman, S Choufan, S Lou, Y Zhao, C Rajendram, R Abidi, FE Skinner, C Hamilton, J Scherer, SW Schwartz, CE Weksberg, R	2011
	Sequence analysis and chromosomal localization of human cap Z. Conserved residues within the actin-binding domain may link cap Z to gelsolin/severin and profilin protein families Journal:Journal of Biological Chemistry	BarronCasella, EA Torres, MA Scherer, SW Heng, HHQ Tsui , LC Casella, JF	1995
	Severe intellectual disability and autistic features associated with microduplication 2q23.1 Journal:European Journal of Human Genetics	Chung, BHY Mullegama, S Marshall, CR Lionel, AC Weksberg, R Dupuis, L Brick, L Li, C Scherer, SW Aradhya, S Stavropoulos, DJ Elsea, SH MendozaLondono, R	2012
	Sex specific methylation differences within the promoter of the non-coding RNA on the chromosome Xp11.4 suggest the maternal imprinted pattern Proceeding/Conference:Annual Meeting of the Organization for the study of Sex Differences, OSDD 2009	Grafodatskay, D Roberts, LJ Zha, CO Lo, Y Chung, BHY Scherer, SW Weksberg, R	2009
	Structure and chromosomal localization of the human constitutive endothelial nitric oxide synthase gene Journal:Journal of Biological Chemistry	Marsden, PA Heng, HHQ Scherer, SW Stewart, RJ Hall, AV Shi , XM Tsui, LC Schappert, KT	1993
	Structure and mapping of the human lanosterol 14α-demethylase gene (CYP51) encoding the cytochrome p450 involved in cholesterol biosynthesis; comparison of exon/intron organization with other mammalian and fungal CYP genes Journal:Genomics	Rozman, D Strömstedt, M Tsui, LC Scherer, SW Waterman, MR	1996
	Translocation breakpoint maps 5 kb 3' from TWIST in a patient affected with Saethre-Chotzen syndrome Journal:Human Molecular Genetics	Krebs, I Weis, I Hudler, M Rommens, JM Roth, H Scherer, SW Tsui, LC Füchtbauer, EM Grzeschik, KH Tsuji, K Kunz, J	1997
	Use of clinical chromosomal microarray in Chinese patients with autism spectrum disorder-implications of a copy number variation involving DPP10 Journal:Molecular Autism	Mak, ASL Chiu, TA Leung, KC Mak, CCY Chu, WY Mok, TKG Tang, WF Chan, YK Tang, MHY Lau, ETK So, KW Tao, QV Fung, CW Wong, CNV Uddin, M Lee, SL Marshall, CR Scherer, SW Kan, ASY Chung, BHY	2017
	Variation in the AU(AT)-rich element within the 3'-untranslated region of PPP1R3 is associated with variation in plasma glucose in aboriginal Canadians Journal:Journal of Clinical Endocrinology and Metabolism	Hegele, RA Harris, SB Zinman, B Wang, J Cao, H Hanley, AJG Tsui, LC Scherer, SW	1998
	The XRCC2 DNA repair gene: Identification of a positional candidate Journal:Genomics	Tambini, CE George, AM Rommens, JM Tsui, LC Scherer, SW Thacker, J	1997
	A YAC-based contig of 1.5 mb spanning the human multidrug resistance gene region and delineating the amplification unit in three human multidrug-resistant cell lines Journal:Genome Research	Torigoe, K Sato, S Kusaba, H Kohno, K Kuwano, M Okumura, K Green, ED Tsui, LC Scherer, SW Schlessinger, D Wada, M	1995

Showing results 94 to 110 of 110 < previous