Fragile X syndrome.

Author:

Turk J

Publisher

BMJ

Subject

Pediatrics, Perinatology and Child Health

Reference41 articles.

1. Identification of a gene (FMR1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome;Verkerk, A.J.M.H.; Pieretti, M.; Sutcliffe, J.S.;Cell,1991

2. Direct diagnosis by DNA analysis of the fragile X syndrome of mental retardation;Rousseau, F.; Heitz, D.; Biancalana, V.;N Engl Jf Med,1991

3. The fragile X syndrome: recent developments;Turk, J.;Current Opinion in Psychiatry,1992

4. The fragile X syndrome;Turk, J.; Hagerman, R.J.; Barnicoat, A.; McEvoy, J.,1994

5. Girls with fragile X syndrome: physical and neurocognitive status and outcome;Hagerman, R.J.; Jackson, C.; Amiri, K.; Cronister-Silverman, A.; O'Connor, R.; Sobesky, W.;Pediatrics,1992

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1. The Behavioral Profile of SYNGAP1-Related Intellectual Disability;American Journal on Intellectual and Developmental Disabilities;2024-04-25

2. El síndrome X frágil: identificación del fenotipo y propuestas educativas;Revista Española de Discapacidad;2014-12

3. Recent advances in behavioural phenotypes as they affect adults;Advances in Mental Health and Intellectual Disabilities;2011-07-15

4. Clinical features of boys with fragile X premutations and intermediate alleles;American Journal of Medical Genetics;2003-07-30

5. Longitudinal course of behavioral and emotional problems in fragile X syndrome;American Journal of Medical Genetics;1999-12-22

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