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Recombination and maternal age-dependent nondisjunction: molecular studies of trisomy 16.
Hassold T, Merrill M, Adkins K, Freeman S, Sherman S. Hassold T, et al. Among authors: sherman s. Am J Hum Genet. 1995 Oct;57(4):867-74. Am J Hum Genet. 1995. PMID: 7573048 Free PMC article.
Correction of the evaluation of recombination in meiosis I and II nondisjunction in trisomy 21.
Sherman S. Sherman S. Am J Hum Genet. 1992 May;50(5):1137-8. Am J Hum Genet. 1992. PMID: 1533301 Free PMC article. No abstract available.
Characterization of a highly polymorphic dinucleotide repeat 150 KB proximal to the fragile X site.
Riggins GJ, Sherman SL, Oostra BA, Sutcliffe JS, Feitell D, Nelson DL, van Oost BA, Smits AP, Ramos FJ, Pfendner E, et al. Riggins GJ, et al. Among authors: sherman sl. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):237-43. doi: 10.1002/ajmg.1320430138. Am J Med Genet. 1992. PMID: 1605197
Collaborative prospective study of the fragile X syndrome: one-year progress report.
Sherman SL, Barbi G, Brøndum-Nielsen K, Brown WT, Carpenter NJ, Chudley AE, Ferraz OP, Ferreira P, Gustavson KH, Halliday J, et al. Sherman SL, et al. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):355-60. doi: 10.1002/ajmg.1320430155. Am J Med Genet. 1992. PMID: 1605212
Although tests of significance were limited due to small sample sizes in subgroups, the following trends were observed: 1) the penetrance of fra(X) site expression was 80% in both male and female conceptuses suggesting that fra(X) site expression is equally penetrant early in dev …
Although tests of significance were limited due to small sample sizes in subgroups, the following trends were observed: 1) the penetrance of …
Conference report: Fourth International Workshop on the fragile X and X-linked mental retardation.
Brown WT, Jenkins E, Neri G, Lubs H, Shapiro LR, Davies KE, Sherman S, Hagerman R, Laird C. Brown WT, et al. Among authors: sherman s. Am J Med Genet. 1991 Feb-Mar;38(2-3):158-72. doi: 10.1002/ajmg.1320380202. Am J Med Genet. 1991. PMID: 1673296 No abstract available.
XY chromosome nondisjunction in man is associated with diminished recombination in the pseudoautosomal region.
Hassold TJ, Sherman SL, Pettay D, Page DC, Jacobs PA. Hassold TJ, et al. Among authors: sherman sl. Am J Hum Genet. 1991 Aug;49(2):253-60. Am J Hum Genet. 1991. PMID: 1867189 Free PMC article.
Collaborative prospective study of the fragile X syndrome: request for participation.
Sherman SL. Sherman SL. Am J Med Genet. 1991 Feb-Mar;38(2-3):396-9. doi: 10.1002/ajmg.1320380248. Am J Med Genet. 1991. PMID: 2018079
Non-disjunction of chromosome 21 in maternal meiosis I: evidence for a maternal age-dependent mechanism involving reduced recombination.
Sherman SL, Petersen MB, Freeman SB, Hersey J, Pettay D, Taft L, Frantzen M, Mikkelsen M, Hassold TJ. Sherman SL, et al. Hum Mol Genet. 1994 Sep;3(9):1529-35. doi: 10.1093/hmg/3.9.1529. Hum Mol Genet. 1994. PMID: 7833907
Methods for genetic linkage analysis using trisomies.
Feingold E, Lamb NE, Sherman SL. Feingold E, et al. Among authors: sherman sl. Am J Hum Genet. 1995 Feb;56(2):475-83. Am J Hum Genet. 1995. PMID: 7847384 Free PMC article.
Nondisjunction of human acrocentric chromosomes: studies of 432 trisomic fetuses and liveborns.
Zaragoza MV, Jacobs PA, James RS, Rogan P, Sherman S, Hassold T. Zaragoza MV, et al. Among authors: sherman s. Hum Genet. 1994 Oct;94(4):411-7. doi: 10.1007/BF00201603. Hum Genet. 1994. PMID: 7927339
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