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Results: 1-11 |
Results: 11

Authors: NOLIN SL HOUCK GE BLUMSTEIN H YE LL DOBKIN CS BROWN WT
Citation: Sl. Nolin et al., SINGLE-CELL ANALYSIS SHOWS DIFFERENT FMR1 CGG REPEAT STABILITY IN SPERM AND LYMPHOCYTES OF PREMUTATION MALES, American journal of human genetics, 61(4), 1997, pp. 1848-1848

Authors: BROWN WT HOUCK GE DING XH ZHONG N NOLIN S GLICKSMAN A DOBKIN C JENKINS EC
Citation: Wt. Brown et al., REVERSE MUTATIONS IN THE FRAGILE-X SYNDROME, American journal of medical genetics, 64(2), 1996, pp. 287-292

Authors: NOLIN SL LEWIS FA YE LL HOUCK GE GLICKSMAN AE LIMPRASERT P LI SY ZHONG N ASHLEY AE FEINGOLD E SHERMAN SL BROWN WT
Citation: Sl. Nolin et al., FAMILIAL TRANSMISSION OF THE FMR1 CGG REPEAT, American journal of human genetics, 59(6), 1996, pp. 1252-1261

Authors: JENKINS EC DOBKIN CS DING X LI SY HOUCK GE BROWN T
Citation: Ec. Jenkins et al., THRESHOLD CGG REPEAT SIZE FOR FRAGILE SITE EXPRESSION WITHOUT METHYLATION IDENTIFIED IN LYMPHOCYTE, LYMPHOBLASTOID AND CLONAL LYMPHOBLASTOID CULTURES FROM AN FMR1 UNMETHYLATED MOSAIC FULL MUTATION INDIVIDUAL, American journal of human genetics, 57(4), 1995, pp. 655-655

Authors: NOLIN SL GLICKSMAN A LEWIS FA YE LL HOUCK GE ASHLEY AE SHERMAN SL BROWN WT
Citation: Sl. Nolin et al., EVIDENCE FOR A FAMILIAL FACTOR INVOLVED IN CGG REPEAT EXPANSION IN FRAGILE-X SYNDROME, American journal of human genetics, 57(4), 1995, pp. 965-965

Authors: ZHONG N LIU XX GOU S HOUCK GE LI SY DOBKIN C BROWN WT
Citation: N. Zhong et al., DISTRIBUTION OF FMR-1 AND ASSOCIATED MICROSATELLITE ALLELES IN A NORMAL CHINESE POPULATION, American journal of medical genetics, 51(4), 1994, pp. 417-422

Authors: JENKINS EC MORYS I HENDERSON J GENOVESE M CARTER M LI SY HOUCK GE DING XH STARKHOUCK SL DOBKIN CS BROWN WT
Citation: Ec. Jenkins et al., FRAGILE-X INDUCTION SYSTEMS IN CVS CULTURES - EFFECT ON CYTOGENETIC, PCR, AND GENOMIC SOUTHERN BLOT DNA ANALYSES OF THE FMR-1 GENE, American journal of medical genetics, 51(4), 1994, pp. 436-442

Authors: NOLIN SL GLICKSMAN A HOUCK GE BROWN WT DOBKIN CS
Citation: Sl. Nolin et al., MOSAICISM IN FRAGILE-X AFFECTED MALES, American journal of medical genetics, 51(4), 1994, pp. 509-512

Authors: BROWN WT HOUCK GE JEZIOROWSKA A LEVINSON FN DING X DOBKIN C ZHONG N HENDERSON J BROOKS SS JENKINS EC
Citation: Wt. Brown et al., RAPID FRAGILE-X CARRIER SCREENING AND PRENATAL-DIAGNOSIS USING A NONRADIOACTIVE PCR TEST (VOL 270, PG 1569, 1993), JAMA, the journal of the American Medical Association, 271(1), 1994, pp. 28-28

Authors: BROWN WT HOUCK GE JEZIOROWSKA A LEVINSON FN DING XH DOBKIN C ZHONG N HENDERSON J BROOKS SS JENKINS EC
Citation: Wt. Brown et al., RAPID FRAGILE-X CARRIER SCREENING AND PRENATAL-DIAGNOSIS USING A NONRADIOACTIVE PCR TEST, JAMA, the journal of the American Medical Association, 270(13), 1993, pp. 1569-1575

Authors: NOLIN SL HOUCK GE LI SY DING XH BROWN WT DOBKIN CS
Citation: Sl. Nolin et al., MOSAICISM IN FRAGILE-X AFFECTED MALES, American journal of human genetics, 53(3), 1993, pp. 1208-1208
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