Fragile X syndrome a case report of a family.

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dc.contributor.authorChatterjee, Cen_US
dc.contributor.authorGuha, Den_US
dc.contributor.authorDas, Sen_US
dc.contributor.authorSingh, S Ken_US
dc.contributor.authorDasgupta, Uen_US
dc.contributor.authorSaha, Sen_US
dc.contributor.authorBannerjee, Den_US
dc.date.accessioned2001-10-31en_US
dc.date.accessioned2009-05-29T11:32:35Z
dc.date.available2001-10-31en_US
dc.date.available2009-05-29T11:32:35Z
dc.date.issued2001-10-31en_US
dc.description.abstractFragile X syndrome is the most common of the inherited disorders causing mental retardation. This disorder results from an abnormal expansion in (CGG)n in repeat found in the coding sequence of the FMRI gene, located at Xq 27.3. Previously it was detected by Karyotyping. With the advent of Molecular Biology PCR, has become the best method in the diagnosis of this disorder. This is a case report of a family with this disorder detected by PCR.en_US
dc.description.affiliationDepartment of Pathology, IPGME&R, Neurology B.I.N., & Molecular Biology Rajabazar Science College.en_US
dc.identifier.citationChatterjee C, Guha D, Das S, Singh SK, Dasgupta U, Saha S, Bannerjee D. Fragile X syndrome a case report of a family. Indian Journal of Pathology & Microbiology. 2001 Oct; 44(4): 499-502en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/73628
dc.language.isoengen_US
dc.source.urihttps://www.ijpmonline.orgen_US
dc.subject.meshAdolescenten_US
dc.subject.meshAdulten_US
dc.subject.meshChilden_US
dc.subject.meshDNA --analysisen_US
dc.subject.meshFamily Healthen_US
dc.subject.meshFemaleen_US
dc.subject.meshFragile X Mental Retardation Proteinen_US
dc.subject.meshFragile X Syndrome --diagnosisen_US
dc.subject.meshHumansen_US
dc.subject.meshMaleen_US
dc.subject.meshMental Retardation --diagnosisen_US
dc.subject.meshMiddle Ageden_US
dc.subject.meshNerve Tissue Proteins --geneticsen_US
dc.subject.meshPolymerase Chain Reactionen_US
dc.subject.meshRNA-Binding Proteinsen_US
dc.subject.meshSex Chromosome Aberrationsen_US
dc.subject.meshTrinucleotide Repeat Expansion --geneticsen_US
dc.subject.meshX Chromosome --geneticsen_US
dc.titleFragile X syndrome a case report of a family.en_US
dc.typeCase Reportsen_US
dc.typeJournal Articleen_US
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