An assessment of screening strategies for fragile X syndrome in the UK.

Pembrey ME, Barnicoat AJ, Carmichael B, Bobrow M, Turner G

Health Technol Assess, (7):1-95 2001

MED: 11262423

Cognitive functioning and information processing of adult mentally retarded men with fragile-X syndrome.

Maes B, Fryns JP, Van Walleghem M, Van den Berghe H

Am J Med Genet, (2):190-200 1994

MED: 8010351

Title not supplied

Hagerman

2002

Relationship of deficits of FMR1 gene specific protein with physical phenotype of fragile X males and females in pedigrees: a new perspective.

Loesch DZ, Huggins RM, Bui QM, Taylor AK, Hagerman RJ

Am J Med Genet A, (2):127-134 2003

MED: 12655493

Fragile X syndrome and deletions in FMR1: new case and review of the literature.

Hammond LS, Macias MM, Tarleton JC, Shashidhar Pai G

Am J Med Genet, (4):430-434 1997

MED: 9375726

A decade of molecular studies of fragile X syndrome.

O'Donnell WT, Warren ST

Annu Rev Neurosci, 315-338 2002

MED: 12052912

American College of Medical Genetics

Fragile

Am J Med Genet 1994

Births: final data for 2002.

Martin JA, Hamilton BE, Sutton PD, Ventura SJ, Menacker F, Munson ML

Natl Vital Stat Rep, (10):1-113 2003

MED: 14717305

Technical standards and guidelines for fragile X: the first of a series of disease-specific supplements to the Standards and Guidelines for Clinical Genetics Laboratories of the American College of Medical Genetics. Quality Assurance Subcommittee of the Laboratory Practice Committee.

Maddalena A, Richards CS, McGinniss MJ, Brothman A, Desnick RJ, Grier RE, Hirsch B, Jacky P, McDowell GA, Popovich B, Watson M, Wolff DJ

Genet Med, (3):200-205 2001

MED: 11388762

Fragile-X carrier screening and the prevalence of premutation and full-mutation carriers in Israel.

Toledano-Alhadef H, Basel-Vanagaite L, Magal N, Davidov B, Ehrlich S, Drasinover V, Taub E, Halpern GJ, Ginott N, Shohat M

Am J Hum Genet, (2):351-360 2001

MED: 11443541