Folic acid metabolism in patient with fragile X

Author:

Nielsen Karen Brøndum,Tommerup Niels,Fariis Brigitte,Hippe Erik

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference11 articles.

1. A simpilified lymphocyte dU (deoxyuridine) suppresion test which can use finger-stick peripheral blood;Das;Clin. Res.,1978

2. FUdR induction of the X chromosome fragile site: Evidence for the mechanism of folic acid and thymidine inhibition;Glover;Amer. J. hum. Genet.,1981

3. Tratment of fragile X;Harpey;Paediatrics,1982

4. Vitamin B12 absorption determined with a double isotope technique employing incomplete stool colleciton;Hjelt;Acta med. scand.,1977

5. Lejeune , J. C. Maunoury M. O. Rethoré M. Prieur O. Raoul 1981 Site fragile Xq27 et métabolisme des monocarbonés. Diminution significative de la fréquence de la lacune chromosomique par tratitment in vitro et in vivo C. R. acad. Sc. Paris. Série 3 491 493

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1. Folate treatment of a boy with fragile-X syndrome;Journal of Intellectual Disability Research;2008-06-28

2. Effect of folic acid treatment in the fragile X syndrome;Clinical Genetics;2008-04-23

3. The neuroanatomy and neuroendocrinology of fragile X syndrome;Mental Retardation and Developmental Disabilities Research Reviews;2004

4. 9 Effects of folate deficiency on embryonic development;Baillière's Clinical Haematology;1995-09

5. Fragile X syndrome;Current Problems in Pediatrics;1987-11

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