2003, Number 4
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Gac Med Mex 2003; 139 (4)
Usefulness of Molecular Biology techniques in Diagnosis of Fragile X-Syndrome.
Rosales-Reynoso MA, Barros-Núñez P
Language: Spanish
References: 5
Page: 413-414
PDF size: 33.67 Kb.
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REFERENCES
Warren ST and Sherman S. The Fragile X syndrome. En: The metabolic basis of inherited disease. Scriver CR, Beaudet AL, Sly Ws, Valle D. (Eds). Mc Graw Hill. Inc. 8va. Edition New York, 2001. p. 1257-1290
Brow WT. The molecular biology of the fragile X mutation. En: Hagerman RJ, Cronister Fragile X syndrome: Diagnosis, treatment and research. Johns Hopkins University Press, Baltimore, MD, 1996. p. 88-113.
Condorelli DF, Dell MG et al. Routine clinical application of the FRAXA PFU PCR assay: Limits and utility. Clin Genet. 1996;50:366-371.
Gold B, Radu D, Balanko A, Chiang CS. Diagnosis of Fragile X Syndrome by Southern blot Hybridization using a chemiluminiscent probe: A Laboratory protocol. Mol Diag 2000;5:169-178.
Weinhausel A, Hass OA. Evaluation of the fragile X (FRAXA) syndrome with methylation-sensitive PCR. Hum Genet. 2001;108:450-458.
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