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Results:
1-15
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Results: 15
Authors:
Crawford, DC
Acuna, JM
Sherman, SL
Citation: Dc. Crawford et al., FMR1 and the fragile X syndrome: Human genome epidemiology review, GENET MED, 3(5), 2001, pp. 359-371
Authors:
Li, JM
Sherman, SL
Lamb, N
Zhao, HY
Citation: Jm. Li et al., Multipoint genetic mapping with trisomy data, AM J HU GEN, 69(6), 2001, pp. 1255-1265
Authors:
Brown, AS
Feingold, E
Broman, KW
Sherman, SL
Citation: As. Brown et al., Genome-wide variation in recombination in female meiosis: a risk factor for non-disjunction of chromosome 21, HUM MOL GEN, 9(4), 2000, pp. 515-523
Authors:
Crawford, DC
Wilson, B
Sherman, SL
Citation: Dc. Crawford et al., Factors involved in the initial mutation of the fragile X CGG repeat as determined by sperm small pool PCR, HUM MOL GEN, 9(19), 2000, pp. 2909-2918
Authors:
Crawford, DC
Zhang, FP
Wilson, B
Warren, ST
Sherman, SL
Citation: Dc. Crawford et al., Fragile X CGG repeat structures among African-Americans: identification ofa novel factor responsible for repeat instability, HUM MOL GEN, 9(12), 2000, pp. 1759-1769
Authors:
Sherman, SL
Citation: Sl. Sherman, Premature ovarian failure in the fragile X syndrome, AM J MED G, 97(3), 2000, pp. 189-194
Authors:
Hobbs, CA
Sherman, SL
Yi, P
Hopkins, SE
Torfs, CP
Hine, RJ
Pogribna, M
Rozen, R
James, SJ
Citation: Ca. Hobbs et al., Polymorphisms in genes involved in folate metabolism as maternal risk factors for Down syndrome, AM J HU GEN, 67(3), 2000, pp. 623-630
Authors:
Sherman, SL
Citation: Sl. Sherman, Premature ovarian failure among fragile X premutation carriers: Parent-of-origin effect?, AM J HU GEN, 67(1), 2000, pp. 11-13
Authors:
Freeman, SB
Yang, QH
Allran, K
Taft, LF
Sherman, SL
Citation: Sb. Freeman et al., Women with a reduced ovarian complement may have an increased risk for a child with Down syndrome, AM J HU GEN, 66(5), 2000, pp. 1680-1683
Authors:
Feingold, E
Brown, AS
Sherman, SL
Citation: E. Feingold et al., Multipoint estimation of genetic maps for human trisomies with one parent or other partial data, AM J HU GEN, 66(3), 2000, pp. 958-968
Authors:
Crawford, DC
Schwartz, CE
Meadows, KL
Newman, JL
Taft, LF
Gunter, C
Brown, WT
Carpenter, NJ
Howard-Peebles, PN
Monaghan, KG
Nolin, SL
Reiss, AL
Feldman, GL
Rohlfs, EM
Warren, ST
Sherman, SL
Citation: Dc. Crawford et al., Survey of the fragile X syndrome CGG repeat and the short-tendem-repeat and single-nucleotide-polymorphism haplotypes in an African American population, AM J HU GEN, 66(2), 2000, pp. 480-493
Authors:
Yang, QH
Sherman, SL
Hassold, TJ
Allran, K
Taft, L
Pettay, D
Khoury, MJ
Erickson, JD
Freeman, SB
Citation: Qh. Yang et al., Risk factors for trisomy 21: Maternal cigarette smoking and oral contraceptive use in a population based case control study, GENET MED, 1(3), 1999, pp. 80-88
Authors:
Crawford, DC
Meadows, KL
Newman, JL
Taft, LF
Pettay, DL
Gold, LB
Hersey, SJ
Hinkle, EF
Stanfield, ML
Holmgreen, P
Yeargin-Allsopp, M
Boyle, C
Sherman, SL
Citation: Dc. Crawford et al., Prevalence and phenotype consequence of FRAXA and FRAXE alleles in a large, ethnically diverse, special education-needs population, AM J HU GEN, 64(2), 1999, pp. 495-507
Authors:
Huggins, RM
Loesch, DZ
Sherman, SL
Citation: Rm. Huggins et al., A branching non-linear autoregressive model for the transmission of the fragile X dynamic repeat mutation, ANN HUM GEN, 62, 1998, pp. 337-347
Authors:
Waldman, ID
Rowe, DC
Abramowitz, A
Kozel, ST
Mohr, JH
Sherman, SL
Cleveland, HH
Sanders, ML
Card, JHC
Stever, C
Citation: Id. Waldman et al., Association and linkage of the dopamine transporter gene and attention-deficit hyperactivity disorder in children: Heterogeneity owing to diagnostic subtype and severity, AM J HU GEN, 63(6), 1998, pp. 1767-1776
Risultati:
1-15
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