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Results: 1-10 |
Results: 10
PCR-based methylation testing for Prader-Willi or Angelman syndromes usingarchived fixed-cell suspensions
Authors: Velinov, M Gu, H Shah, K Genovese, M Duncan, C Kupchik, G Jenkins, EC
Citation: M. Velinov et al., PCR-based methylation testing for Prader-Willi or Angelman syndromes usingarchived fixed-cell suspensions, GENET TEST, 5(2), 2001, pp. 153-155
Molecular diagnosis of and carrier screening for the neuronal ceroid lipofuscinoses
Authors: Zhong, NA Wisniewski, KE Ju, WN Moroziewicz, DN Jurkiewicz, A McLendon, L Jenkins, EC Brown, WT
Citation: Na. Zhong et al., Molecular diagnosis of and carrier screening for the neuronal ceroid lipofuscinoses, GENET TEST, 4(3), 2000, pp. 243-248
Distribution of apolipoprotein E genotypes in fragile X syndrome and Batten disease
Authors: Zhong, N Ju, WN Brown, WT Ye, LL Jenkins, EC Schupf, N
Citation: N. Zhong et al., Distribution of apolipoprotein E genotypes in fragile X syndrome and Batten disease, AM J MED G, 84(3), 1999, pp. 309-310
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
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
Ultrastructure of the fragile X chromosome: New observations on the fragile site
Authors: Wen, GY Jenkins, EC Goldberg, EM Genovese, M Brown, WT Wisniewski, HM
Citation: Gy. Wen et al., Ultrastructure of the fragile X chromosome: New observations on the fragile site, AM J MED G, 83(4), 1999, pp. 331-333
First transmission electron micrograph of continuous mitotic spindle fibers between polar area and chromosome ends
Authors: Wen, GY Jenkins, EC Goldberg, EM Genovese, M Brown, WT Wisniewski, HM
Citation: Gy. Wen et al., First transmission electron micrograph of continuous mitotic spindle fibers between polar area and chromosome ends, AM J MED G, 83(4), 1999, pp. 334-337
Accelerated prenatal diagnosis of fragile X syndrome by polymerase chain reaction restriction fragment detection
Authors: Dobkin, C Ding, XH Li, SY Houck, G Nolin, SL Glicksman, A Zhong, N Jenkins, EC Brown, WT
Citation: C. Dobkin et al., Accelerated prenatal diagnosis of fragile X syndrome by polymerase chain reaction restriction fragment detection, AM J MED G, 83(4), 1999, pp. 338-341
Prenatal fragile X detection using cytoplasmic and nuclear-specific monoclonal antibodies
Authors: Jenkins, EC Wen, GY Kim, KS Zhong, N Sapienza, VJ Hong, H Chen, J Li, SY Houck, GE Ding, XH Nolin, SL Dobkin, CS Brown, WT
Citation: Ec. Jenkins et al., Prenatal fragile X detection using cytoplasmic and nuclear-specific monoclonal antibodies, AM J MED G, 83(4), 1999, pp. 342-346
Mitotic index and Alzheimer's disease
Authors: Jenkins, EC Ye, LL Gu, H Wisniewski, HM
Citation: Ec. Jenkins et al., Mitotic index and Alzheimer's disease, NEUROREPORT, 9(17), 1998, pp. 3857-3861
Risultati: 1-10 |