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Title	Author(s)	Issue Date	Views
A panel of radiation hybrids defining the 7q31-q32 region of human chromosome 7 Journal:DNA Research	Nakabayashi, K Ogata, T Fujii, M Takahashi, EI Ogino, H Migihshita, E Scherer, SW Tsui, LC Ayusawa, D	1996	138
Paraoxonase-2 G148 variant in an aboriginal Canadian girl with non-insulin-dependent diabetes [7] Journal:Lancet	Hegele, RA Connelly, PW Scherer, SW Hanley, AJG Harris, SB Tsui, LC Zinman, B	1997	196
Paraoxonase-2 gene (PON2) G148 variant associated with elevated fasting plasma glucose in noninsulin-dependent diabetes mellitus Journal:Journal of Clinical Endocrinology and Metabolism	Hegele, RA Connelly, PW Scherer, SW Hanley, AJG Harris, SB Tsui, LC Zinman, B	1997	153
Paternal uniparental disomy of chromosome 19 in a pair of monochorionic diamniotic twins with dysmorphic features and developmental delay Journal:Journal of Medical Genetics	Yeung, KS Ho, SP Lee, SL Kan, SYA Chan, YK Tang, MHY MAK, CCY Leung, KC So, PL Pfundt, R Marshall, CR Scherer, SW Choufani, S Weksberg, R Chung, BHY	2018	79
Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder Journal:Journal of Medical Genetics	Fernandez, BA Roberts, W Chung, B Weksberg, R Meyn, S Szatmari, P JosephGeorge, AM MacKay, S Whitten, K Noble, B Vardy, C Crosbie, V Luscombe, S Tucker, E Turner, L Marshall, CR Scherer, SW	2010	195
Phenotypic spectrum associated with duplication of Xp11.22-p11.23 includes Autism Spectrum Disorder Journal:European Journal of Medical Genetics	Chung, BHY Drmic, I Marshall, CR Grafodatskaya, D Carter, M Fernandez, BA Weksberg, R Roberts, W Scherer, SW	2011	139
Phenotypic spectrum associated with PTCHD1 deletion and truncating mutations includes intellectual disability and autism spectrum disorder Journal:Clinical Genetics	Chaudhry, A Noor, A Degagne, B Baker, K Bok, LA Brady, AF Chitayat, D Chung, BHY Cytrynbaum, C Dyment, D Filges, I Helm, B Hutchison, HT Jeng, LJB Laumonnier, F Marshall, CR Menzel, M Parkash, S Parker, MJ The, DDD STUDY Raymond, FL Rideout, AL Roberts, W Rupps, R Schanze, I Schrander-Stumpel, CTRM Speevak, MD Stavropoulos, DJ Stevens, SJC Thomas, ERA Toutain, A Vergano, S Weksberg, R Scherer, SW Vincent, JB Carter, MT	2015	61
Physical mapping of a tandem duplication on the long arm of chromosome 7 associated with a multidrug resistant phenotype Journal:Cancer Genetics and Cytogenetics	De Silva, MG Kantharidis, P Scherer, SW Rayeroux, K Campbell, L Tsui, LC Zalcberg, JR	1999	124
Physical mapping of the chromosome 7 breakpoint region in an SLOS Patient with t(7;20)(q32.1;q!3.2) Journal:American Journal of Medical Genetics	Alley, TL Scherer, SW Huizenga, JJ Tsui, LC Wallace, MR	1997	177
Physical mapping of the holoprosencephaly critical region on chromosome 7q36 Journal:Nature Genetics	Gurrieri, F Trask, BJ Van Den Engh, G Krauss, CM Schinzel, A Pettenati, MJ Schindler, D DietzBand, J Vergnaud, G Scherer, SW Tsui, LC Muenke, M	1993	104
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	148
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	163
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	207
Positional candidate genes for congenital chloride diarrhea suggested by high-resolution physical mapping in chromosome region 7q31 Journal:Genome Research	Höglund, P Haila, S Scherer, SW Tsui, LC Green, ED Weissenbach, J Holmberg, C De La Chapelle, A Kere, J	1996	139
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	56
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	187
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	196
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	168
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	128
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	122

Showing results 80 to 99 of 110 < previous next >