Literature DB >> 1346284

Detection of full fragile X mutation.

R G Pergolizzi1, S H Erster, P Goonewardena, W T Brown.   

Abstract

In fragile X syndrome, the most common inherited cause of mental deficiency, the underlying mutation is a large increase in the number of CGG repeats in a gene on chromosome X. We have developed a polymerase chain reaction (PCR) method to amplify across the full mutation in affected individuals. In this report, a fragile X family including a positive prenatally diagnosed fetus was analysed by PCR, and the results are consistent with direct genomic Southern blot analysis. Genetic screening of at-risk populations for fragile X can now be achieved by PCR rapidly, inexpensively, and on small samples.

Entities:  

Mesh:

Substances:

Year:  1992        PMID: 1346284     DOI: 10.1016/0140-6736(92)91334-5

Source DB:  PubMed          Journal:  Lancet        ISSN: 0140-6736            Impact factor:   79.321


  16 in total

1.  RS46(DXS548) genotyping of reproductive cells: approaching preimplantation testing of the fragile-X syndrome.

Authors:  J C Dreesen; J P Geraedts; J C Dumoulin; J L Evers; M H Pieters
Journal:  Hum Genet       Date:  1995-09       Impact factor: 4.132

Review 2.  Who should be offered genetic screening?

Authors:  M Super
Journal:  Postgrad Med J       Date:  1993-09       Impact factor: 2.401

3.  Molecular genetic analysis of mentally retarded males with features of the fragile-X syndrome.

Authors:  M G Butler; R Pratesi; C L Vnencak-Jones
Journal:  J Intellect Disabil Res       Date:  1995-12

Review 4.  Recent advances in assays for the fragile X-related disorders.

Authors:  Bruce E Hayward; Daman Kumari; Karen Usdin
Journal:  Hum Genet       Date:  2017-09-02       Impact factor: 4.132

5.  PCR bias in amplification of androgen receptor alleles, a trinucleotide repeat marker used in clonality studies.

Authors:  G L Mutter; K A Boynton
Journal:  Nucleic Acids Res       Date:  1995-04-25       Impact factor: 16.971

6.  A PCR-based test suitable for screening for fragile X syndrome among mentally retarded males.

Authors:  L A Haddad; R C Mingroni-Netto; A M Vianna-Morgante; S D Pena
Journal:  Hum Genet       Date:  1996-06       Impact factor: 4.132

7.  Anthropometric and craniofacial patterns in mentally retarded males with emphasis on the fragile X syndrome.

Authors:  M G Butler; R Pratesi; M S Watson; W R Breg; D N Singh
Journal:  Clin Genet       Date:  1993-09       Impact factor: 4.438

8.  Consensus characterization of 16 FMR1 reference materials: a consortium study.

Authors:  Jean Amos Wilson; Victoria M Pratt; Amit Phansalkar; Kasinathan Muralidharan; W Edward Highsmith; Jeanne C Beck; Scott Bridgeman; Ebony M Courtney; Lidia Epp; Andrea Ferreira-Gonzalez; Nick L Hjelm; Leonard M Holtegaard; Mohamed A Jama; John P Jakupciak; Monique A Johnson; Paul Labrousse; Elaine Lyon; Thomas W Prior; C Sue Richards; Kristy L Richie; Benjamin B Roa; Elizabeth M Rohlfs; Tina Sellers; Stephanie L Sherman; Karen A Siegrist; Lawrence M Silverman; Joanna Wiszniewska; Lisa V Kalman
Journal:  J Mol Diagn       Date:  2007-12-28       Impact factor: 5.568

9.  Direct versus indirect molecular diagnosis of fragile X mental retardation in 40 German families at risk.

Authors:  O Knobloch; F Pelz; U Wick; D L Nelson; B Zoll
Journal:  J Med Genet       Date:  1993-03       Impact factor: 6.318

10.  Inheritance of the fragile X syndrome: size of the fragile X premutation is a major determinant of the transition to full mutation.

Authors:  D Heitz; D Devys; G Imbert; C Kretz; J L Mandel
Journal:  J Med Genet       Date:  1992-11       Impact factor: 6.318

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.