Possible association of rare autosomal folate sensitive fragile sites and idiopathic mental retardation: a blind controlled population study
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1990.tb03577.x/fullpdf
Reference46 articles.
1. A fragile secondary constriction on chromosome 2 in 5 patients with different clinical features;Anneren;Hereditas,1981
2. Report on the committee on chromosome rearrangements in neoplasms and on fragile sites. (HGM8);Berger;Cytogenet. Cell Genet.,1985
3. Sex chromosome aneuploidy in fragile X carriers;Brøndum Nielsen;Am. J. Med. Genet.,1986
4. Fragile 19 p13 in a family with mental illness;Chodirker;Clin. Genet.,1987
5. Fragile X syndrome;Chudley;J. Pediatr.,1987
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1. Fragile Sites and Human Disease;eLS;2009-03-15
2. Diagnostic investigations in individuals with mental retardation: a systematic literature review of their usefulness;European Journal of Human Genetics;2004-11-03
3. Mental retardation with rare fragile site expressed at 2q11;Brain and Development;2000-12
4. Increased expression of aphidicolin-induced common fragile sites in Tourette syndrome: The key to understand the genetics of comorbid phenotypes?;American Journal of Medical Genetics;1996-02-16
5. Cytogenetics of autosomal fragile sites: A Basque population study;American Journal of Human Biology;1996
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