| Rapid antibody test for fragile X syndrome. | |
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MedLine Citation:
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PMID: 7723547 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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Fragile X syndrome is the most common known cause of inherited mental retardation. Identification of patients and carriers of fragile X syndrome is usually done with a DNA test system but we have developed a rapid antibody to identify fragile X patients. This non-invasive test requires only 1 or 2 drops of blood and can be used for screening large groups of mentally retarded people and neonates for fragile X syndrome. |
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Authors:
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R Willemsen; S Mohkamsing; B de Vries; D Devys; A van den Ouweland; J L Mandel; H Galjaard; B Oostra |
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Publication Detail:
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Type: Journal Article; Research Support, Non-U.S. Gov't |
Journal Detail:
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Title: Lancet Volume: 345 ISSN: 0140-6736 ISO Abbreviation: Lancet Publication Date: 1995 May |
Date Detail:
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Created Date: 1995-05-24 Completed Date: 1995-05-24 Revised Date: 2006-11-15 |
Medline Journal Info:
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Nlm Unique ID: 2985213R Medline TA: Lancet Country: ENGLAND |
Other Details:
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Languages: eng Pagination: 1147-8 Citation Subset: AIM; IM |
Affiliation:
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Department of Clinical Genetics, Erasmus University, Rotterdam, Netherlands. |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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Antibodies, Monoclonal
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diagnostic use DNA / genetics Female Fragile X Mental Retardation Protein Fragile X Syndrome / blood, diagnosis*, genetics Heterozygote Heterozygote Detection Humans Male Nerve Tissue Proteins / blood RNA-Binding Proteins / blood |
| Chemical | |
Reg. No./Substance:
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0/Antibodies, Monoclonal; 0/FMR1 protein, human; 0/Nerve Tissue Proteins; 0/RNA-Binding Proteins; 139135-51-6/Fragile X Mental Retardation Protein; 9007-49-2/DNA |
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