Literature DB >> 8844072

A rapid, reliable, and inexpensive method for detection of di- and trinucleotide repeat markers and disease loci from dried blood spots.

J J Holden1, M Chalifoux, M Wing, C Julien-Inalsingh, B N White.   

Abstract

We used a rapid and inexpensive method for studying the FMR1 CGG-repeat from dried blood spots, prepared from heel pricks, finger pricks, or an aliquot of blood from a venipuncture. The procedure includes a single tube for preparation of template DNA for PCR and minimal handling, avoiding opportunities for mislabelling specimens and loss of template. We extended the protocol to numerous di- and trinucleotide repeat markers and disease loci, including FRAXE, FRAXF, DXS548, DRPLA, and ZFY. The use of a highly reliable and very inexpensive method which employs blood spots as a source for target DNA means that newborn Guthrie cards can be used to establish allele frequencies for linkage disequilibrium studies, that large populations can be screened for genetic disorders, and that mapping studies can proceed rapidly even when only small amounts of blood are available from key family members.

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Year:  1996        PMID: 8844072     DOI: 10.1002/(SICI)1096-8628(19960809)64:2<313::AID-AJMG16>3.0.CO;2-I

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  4 in total

1.  Linking the FMR1 alleles with small CGG expansions with neurodevelopmental disorders: preliminary data suggest an involvement of epigenetic mechanisms.

Authors:  Danuta Z Loesch; David E Godler; Mahmoud Khaniani; Emma Gould; Freya Gehling; Cheryl Dissanayake; Trent Burgess; Flora Tassone; Richard Huggins; Howard Slater; K H Andy Choo
Journal:  Am J Med Genet A       Date:  2009-10       Impact factor: 2.802

2.  Small CGG repeat expansion alleles of FMR1 gene are associated with parkinsonism.

Authors:  D Z Loesch; M S Khaniani; H R Slater; J P Rubio; Q M Bui; K Kotschet; W D'Souza; A Venn; P Kalitsis; A K H Choo; T Burgess; L Johnson; A Evans; M Horne
Journal:  Clin Genet       Date:  2009-09-30       Impact factor: 4.438

3.  Screening for expanded alleles of the FMR1 gene in blood spots from newborn males in a Spanish population.

Authors:  Isabel Fernandez-Carvajal; Paulina Walichiewicz; Xie Xiaosen; Ruiqin Pan; Paul J Hagerman; Flora Tassone
Journal:  J Mol Diagn       Date:  2009-05-21       Impact factor: 5.568

4.  Identification of microsatellite markers <1 Mb from the FMR1 CGG repeat and development of a single-tube tetradecaplex PCR panel of highly polymorphic markers for preimplantation genetic diagnosis of fragile X syndrome.

Authors:  Min Chen; Mingjue Zhao; Caroline G Lee; Samuel S Chong
Journal:  Genet Med       Date:  2016-01-07       Impact factor: 8.822

  4 in total

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