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Results: 1-12 |
Results: 12
Genetically determined low maternal serum dopamine beta-hydroxylase levelsand the etiology of autism spectrum disorders
Authors: Robinson, PD Schutz, CK Macciardi, F White, BN Holden, JJA
Citation: Pd. Robinson et al., Genetically determined low maternal serum dopamine beta-hydroxylase levelsand the etiology of autism spectrum disorders, AM J MED G, 100(1), 2001, pp. 30-36
Distribution of FMR1 and FMR2 alleles in Javanese individuals with developmental disability and confirmation of a specific AGG-interruption pattern in Asian populations
Authors: Faradz, SMH Leggo, J Murray, A Lam-Po-Tang, PRL Buckley, MF Holden, JJA
Citation: Smh. Faradz et al., Distribution of FMR1 and FMR2 alleles in Javanese individuals with developmental disability and confirmation of a specific AGG-interruption pattern in Asian populations, ANN HUM GEN, 65, 2001, pp. 127-135
Apparently unstable normal FMR1 alleles in nine developmentally delayed patients: Implications for molecular diagnosis of the Fragile X syndrome
Authors: Tzountzouris, J Kennedy, D Skuterud, M Connolly-Wilson, M Holden, JJA Lin, CC Mak-Tam, E Somerville, MJ Summers, AM Allingham-Hawkins, DJ
Citation: J. Tzountzouris et al., Apparently unstable normal FMR1 alleles in nine developmentally delayed patients: Implications for molecular diagnosis of the Fragile X syndrome, GENET TEST, 4(3), 2000, pp. 235-239
Genetic diversity at the FMR1 locus in the Indonesian population
Authors: Faradz, SMH Pattiiha, MZ Leigh, DA Jenkins, M Leggo, J Buckley, MF Holden, JJA
Citation: Smh. Faradz et al., Genetic diversity at the FMR1 locus in the Indonesian population, ANN HUM GEN, 64, 2000, pp. 329-339
Frequencies of "grey-zone"and premutation-size FMR1 CGG-repeat alleles in patients with developmental disability in Cyprus and Canada
Authors: Patsalis, PC Sismani, C Hettinger, JA Holden, JJA Lawson, JS Chalifoux, M Wing, M Walker, M Leggo, J
Citation: Pc. Patsalis et al., Frequencies of "grey-zone"and premutation-size FMR1 CGG-repeat alleles in patients with developmental disability in Cyprus and Canada, AM J MED G, 84(3), 1999, pp. 195-197
Genetic variation and intergenerational FMR1 CGG-repeat stability in 100 unrelated three-generation families from the normal population
Authors: Patsalis, PC Sismani, C Stylianou, S Ioannou, P Joseph, G Manoli, P Holden, JJA Hettinger, JA
Citation: Pc. Patsalis et al., Genetic variation and intergenerational FMR1 CGG-repeat stability in 100 unrelated three-generation families from the normal population, AM J MED G, 84(3), 1999, pp. 217-220
Improved amplification of the FMR2 GCC repeat from dried blood spots
Authors: Leggo, J Holden, JJA
Citation: J. Leggo et Jja. Holden, Improved amplification of the FMR2 GCC repeat from dried blood spots, AM J MED G, 84(3), 1999, pp. 304-305
Eighth International Workshop on the Fragile X Syndrome and X-linked Mental Retardation, August 16-22, 1997
Authors: Holden, JJA Percy, M Allingham-Hawkins, D Brown, WT Chiurazzi, P Fisch, G Gane, L Gunter, C Hagerman, R Jenkins, EC Kooy, RF Lubs, HA Murray, A Neri, G Schwartz, C Tranebjaerg, L Villard, L Willems, PJ
Citation: Jja. Holden et al., Eighth International Workshop on the Fragile X Syndrome and X-linked Mental Retardation, August 16-22, 1997, AM J MED G, 83(4), 1999, pp. 221-236
Longitudinal assessment of adaptive and maladaptive behaviors in fragile Xmales: Growth, development, and profiles
Authors: Fisch, GS Carpenter, NJ Holden, JJA Simensen, R Howard-Peebles, PN Maddalena, A Pandya, A Nance, W
Citation: Gs. Fisch et al., Longitudinal assessment of adaptive and maladaptive behaviors in fragile Xmales: Growth, development, and profiles, AM J MED G, 83(4), 1999, pp. 257-263
Longitudinal changes in cognitive and adaptive behavior in fragile X females: A prospective multicenter analysis
Authors: Fisch, GS Carpenter, N Holden, JJA Howard-Peebles, PN Maddalena, A Borghgraef, M Steyaert, J Fryns, JP
Citation: Gs. Fisch et al., Longitudinal changes in cognitive and adaptive behavior in fragile X females: A prospective multicenter analysis, AM J MED G, 83(4), 1999, pp. 308-312
Fragile X premutation is a significant risk factor for premature ovarian failure: The international collaborative POF in fragile X study - Preliminary data
Authors: Allingham-Hawkins, SJ Babul-Hirji, R Chitayat, D Holden, JJA Yang, KT Lee, C Hudson, R Gorwill, H Nolin, SL Glicksman, A Jenkins, EC Brown, WT Howard-Peebles, PN Becchi, C Cummings, E Fallon, L Seitz, S Black, SH Vianna-Morgante, AM Costa, SS Otto, PA Mingroni-Netto, RC Murray, A Webb, J MacSwinney, F Dennis, N Jacobs, PA Syrrou, M Georgiou, I Patsalis, PC Uzielli, MLG Guarducci, S Lapi, E Cecconi, A Ricci, U
Citation: Sj. Allingham-hawkins et al., Fragile X premutation is a significant risk factor for premature ovarian failure: The international collaborative POF in fragile X study - Preliminary data, AM J MED G, 83(4), 1999, pp. 322-325
Molecular screening for fragile X syndrome among Indonesian children with developmental disability
Authors: Faradz, SMH Buckley, M Tang, LP Leigh, D Holden, JJA
Citation: Smh. Faradz et al., Molecular screening for fragile X syndrome among Indonesian children with developmental disability, AM J MED G, 83(4), 1999, pp. 350-351
Risultati: 1-12 |