Sherman SL - Search Results

1

Genetic diversity of the fragile X syndrome gene (FMR1) in a large Sub-Saharan West African population.

Peprah EK, Allen EG, Williams SM, Woodard LM, Sherman SL. Peprah EK, et al. Among authors: sherman sl. Ann Hum Genet. 2010 Jul;74(4):316-25. doi: 10.1111/j.1469-1809.2010.00582.x. Ann Hum Genet. 2010. PMID: 20597902 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

An n-allele model for progressive amplification in the FMR1 locus.

Morris A, Morton NE, Collins A, Macpherson J, Nelson D, Sherman S. Morris A, et al. Proc Natl Acad Sci U S A. 1995 May 23;92(11):4833-7. doi: 10.1073/pnas.92.11.4833. Proc Natl Acad Sci U S A. 1995. PMID: 7761409 Free PMC article.

6

Normal variation at the myotonic dystrophy locus in global human populations.

Zerylnick C, Torroni A, Sherman SL, Warren ST. Zerylnick C, et al. Among authors: sherman sl. Am J Hum Genet. 1995 Jan;56(1):123-30. Am J Hum Genet. 1995. PMID: 7825567 Free PMC article.

7

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.

8

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

9

Population dynamics of a meiotic/mitotic expansion model for the fragile X syndrome.

Ashley AE, Sherman SL. Ashley AE, et al. Among authors: sherman sl. Am J Hum Genet. 1995 Dec;57(6):1414-25. Am J Hum Genet. 1995. PMID: 8533772 Free PMC article.

10

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

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

441 results

Search Page

Filters