Sherman SL - Search Results

1

The International Fragile X Premutation Registry: building a resource for research and clinical trial readiness.

Hessl D, Rosselot H, Miller R, Espinal G, Famula J, Sherman SL, Todd PK, Cabal Herrera AM, Lipworth K, Cohen J, Hall DA, Leehey M, Grigsby J, Weber JD, Alusi S, Wheeler A, Raspa M, Hudson T, Sobrian SK. Hessl D, et al. Among authors: sherman sl. J Med Genet. 2022 Dec;59(12):1165-1170. doi: 10.1136/jmedgenet-2022-108568. Epub 2022 Jun 14. J Med Genet. 2022. PMID: 35701103 Free PMC article.

2

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

3

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

4

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

5

Characteristics of the transmission of the FMR1 gene from carrier females in a prospective sample of conceptuses.

Sherman SL, Maddalena A, Howard-Peebles PN, Brown WT, Nolin S, Jenkins E, Schwartz C, Tarrelton J, Shapiro LR, Smits AP, et al. Sherman SL, et al. Am J Med Genet. 1994 Jul 15;51(4):503-6. doi: 10.1002/ajmg.1320510442. Am J Med Genet. 1994. PMID: 7943029

6

Examination of factors that influence the expansion of the fragile X mutation in a sample of conceptuses from known carrier females.

Sherman SL, Meadows KL, Ashley AE. Sherman SL, et al. Am J Med Genet. 1996 Aug 9;64(2):256-60. doi: 10.1002/(SICI)1096-8628(19960809)64:2<256::AID-AJMG4>3.0.CO;2-S. Am J Med Genet. 1996. PMID: 8844059

7

Survey of the fragile X syndrome and the fragile X E syndrome in a special education needs population.

Meadows KL, Pettay D, Newman J, Hersey J, Ashley AE, Sherman SL. Meadows KL, et al. Among authors: sherman sl. Am J Med Genet. 1996 Aug 9;64(2):428-33. doi: 10.1002/(SICI)1096-8628(19960809)64:2<428::AID-AJMG39>3.0.CO;2-F. Am J Med Genet. 1996. PMID: 8844098

8

Premature ovarian failure in the fragile X syndrome.

Sherman SL. Sherman SL. Am J Med Genet. 2000 Fall;97(3):189-94. doi: 10.1002/1096-8628(200023)97:3<189::AID-AJMG1036>3.0.CO;2-J. Am J Med Genet. 2000. PMID: 11449487 Review.

9

Prevalence of the fragile X syndrome in African-Americans.

Crawford DC, Meadows KL, Newman JL, Taft LF, Scott E, Leslie M, Shubek L, Holmgreen P, Yeargin-Allsopp M, Boyle C, Sherman SL. Crawford DC, et al. Among authors: sherman sl. Am J Med Genet. 2002 Jul 1;110(3):226-33. doi: 10.1002/ajmg.10427. Am J Med Genet. 2002. PMID: 12116230

10

Detection of early FXTAS motor symptoms using the CATSYS computerised neuromotor test battery.

Allen EG, Juncos J, Letz R, Rusin M, Hamilton D, Novak G, Shubeck L, Tinker SW, Sherman SL. Allen EG, et al. Among authors: sherman sl. J Med Genet. 2008 May;45(5):290-7. doi: 10.1136/jmg.2007.054676. Epub 2008 Jan 30. J Med Genet. 2008. PMID: 18234731 Free PMC article.

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