A new genetic model for the fragile X syndrome involving an autosomal suppressor gene (comments on the paper by M.H. Israel)SHERMAN, S. L.American journal of medical genetics. 1987, Vol 26, Num 1, pp 33-36, issn 0148-7299Article

Collaborative prospective study of the fragile X syndrome : request for participationSHERMAN, S. L.American journal of medical genetics. 1991, Vol 38, Num 2-3, pp 396-399, issn 0148-7299Article

A new genetic model for the fragile X syndrome involving an autosomal suppressor gene (comments on the paper by M.H. Israel)SHERMAN, S. L.American journal of medical genetics. 1987, Vol 26, Num 1, pp 33-36, issn 0148-7299Article

Co-occurring diagnoses among FMR1 premutation allele carriersHUNTER, J. E; ROHR, J. K; SHERMAN, S. L et al.Clinical genetics. 2010, Vol 77, Num 4, pp 374-381, issn 0009-9163, 8 p.Article

Prevalence and phenotype consequence of FRAXA and FRAXE alleles in a large, ethnically diverse, special education-needs populationCRAWFORD, D. C; MEADOWS, K. L; YEARGIN-ALLSOPP, M et al.American journal of human genetics. 1999, Vol 64, Num 2, pp 495-507, issn 0002-9297Article

Association and linkage of the dopamine transporter gene and attention-deficit hyperactivity disorder in children : Heterogeneity owing to diagnostic subtype and severityWALDMAN, I. D; ROWE, D. C; ABRAMOWITZ, A et al.American journal of human genetics. 1998, Vol 63, Num 6, pp 1767-1776, issn 0002-9297Article

Improved prenatal detection of fra(X) (q27.3) : methods for prevention of false negatives in chorionic villus and amniotic fluid cell culturesJENKINS, E. C; KRAWCZUN, M. S; BROWN, W. T et al.American journal of medical genetics. 1991, Vol 38, Num 2-3, pp 447-452, issn 0148-7299Article

Examination of reproductive aging milestones among women who carry the FMR1 premutationALLEN, E. G; SULLIVAN, A. K; MARCUS, M et al.Human reproduction (Oxford. Print). 2007, Vol 22, Num 8, pp 2142-2152, issn 0268-1161, 11 p.Article

Polymorphisms in genes involved in folate metabolism as maternal risk factors for Down syndromeHOBBS, C. A; SHERMAN, S. L; PING YI et al.American journal of human genetics. 2000, Vol 67, Num 3, pp 623-630, issn 0002-9297Article

Women with a reduced ovarian complement may have an increased risk for a child with Down syndromeFREEMAN, S. B; QUANHE YANG; ALLRAN, K et al.American journal of human genetics. 2000, Vol 66, Num 5, pp 1680-1683, issn 0002-9297Conference Paper

Population dynamics of a meiotic/mitotic expansion model for the fragile X syndromeASHLEY, A. E; SHERMAN, S. L.American journal of human genetics. 1995, Vol 57, Num 6, pp 1414-1425, issn 0002-9297Article

Guidelines for human linkage maps. An international system for human linkage maps (ISLM, 1990)KEATS, B. J. B; SHERMAN, S. L; MORTON, N. E et al.Annals of human genetics. 1991, Vol 55, pp 1-6, issn 0003-4800, 6 p., p.1Article

A segregation and linkage study of classical and nonclassical 21-hydroxylase deficiencySHERMAN, S. L; ASTON, C. E; MORTON, N. E et al.American journal of human genetics. 1988, Vol 42, Num 6, pp 830-838, issn 0002-9297Article

Germline mutation of microRNA-125a is associated with breast cancerLI, W; DUAN, R; KOOY, F et al.Journal of medical genetics. 2009, Vol 46, Num 5, pp 358-360, issn 0022-2593, 3 p.Article

Detection of early FXTAS motor symptoms using the CATSYS computerised neuromotor test batteryALLEN, E. G; JUNCOS, J; LETZ, R et al.Journal of medical genetics. 2008, Vol 45, Num 5, pp 290-297, issn 0022-2593, 8 p.Article

Examination of factors associated with instability of the FMR1 CGG repeatASHLEY-KOCH, A. E; ROBINSON, H; GLICKSMAN, A. E et al.American journal of human genetics. 1998, Vol 63, Num 3, pp 776-785, issn 0002-9297Article

Testing for contributions of mitochondrial DNA mutations to complex diseasesFENGZHU SUN; ASHLEY-KOCH, A. E; DURHAM, L. K et al.Genetic epidemiology. 1998, Vol 15, Num 5, pp 451-469, issn 0741-0395Conference Paper

Susceptible chiasmate configurations of chromosome 21 predispose to non-disjunction in both maternal meiosis I and meiosis IILAMB, N. E; FREEMAN, S. B; AVRAMOPOULOS, D et al.Nature genetics. 1996, Vol 14, Num 4, pp 400-405, issn 1061-4036Article

Familial transmission of the FMR1 CGG repeatNOLIN, S. L; LEWIS, F. A; SHERMAN, S. L et al.American journal of human genetics. 1996, Vol 59, Num 6, pp 1252-1261, issn 0002-9297Article

Normal variation at the myotonic dystrophy locus in global human populationsZERYLNICK, C; TORRONI, A; SHERMAN, S. L et al.American journal of human genetics. 1995, Vol 56, Num 1, pp 123-130, issn 0002-9297Article

Startle disease, or hyperekplexia: response to clonazepam and assignment of the gene (STHE) to chromosome 5q by linkage analysisRYAN, S. G; SHERMAN, S. L; TERRY, J. C et al.Annals of neurology. 1992, Vol 31, Num 6, pp 663-668, issn 0364-5134Article

A counseling guide to the Martin-Bell syndromeWEAVER, D. D; SHERMAN, S. L.American journal of medical genetics. 1987, Vol 26, Num 1, pp 39-44, issn 0148-7299Article

Association of FMR1 repeat size with ovarian dysfunctionSULLIVAN, A. K; MARCUS, M; EPSTEIN, M. P et al.Human reproduction (Oxford. Print). 2005, Vol 20, Num 2, pp 402-412, issn 0268-1161, 11 p.Article

A branching non-linear autoregressive model for the transmission of the fragile X dynamic repeat mutationHUGGINS, R. M; LOESCH, D. Z; SHERMAN, S. L et al.Annals of human genetics. 1998, Vol 62, pp 337-347, issn 0003-4800, 4Article

Characterization of susceptible chiasma configurations that increase the risk for maternal nondisjunction of chromosome 21LAMB, N. E; FEINGOLD, E; SAKER, D et al.Human molecular genetics (Print). 1997, Vol 6, Num 9, pp 1391-1399, issn 0964-6906Article