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Molecular diagnosis and genetic counseling for fragile X mental retardation

Pandey U B, Phadke S R, Mittal B

Year : 2004| Volume: 52| Issue : 1 | Page no: 36-42

   This article has been cited by
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2 A simple, high-throughput assay for fragile X expanded alleles using triple repeat primed PCR and capillary electrophoresis
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4 Molecular diagnosis and genetic counselling of fragile X syndrome | [Frajil X sendromunun moleküler tanisi ve genetik danişmanlik]
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6 Technical experiences in the use of immunohistochemical testing for the diagnosis of fragile x syndrome [Experiencias técnicas en el uso de la prueba inmunohistoquí mica para el diagnostico del síndrome de frágil x]
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Online since 20th March '04
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