Literature DB >> 24911126

Methylation analysis in newborn screening for fragile X syndrome.

David E Godler1, David J Amor1, Howard R Slater1.   

Abstract

Entities:  

Mesh：

Year:  2014        PMID： 24911126     DOI： 10.1001/jamaneurol.2014.142

Source DB:  PubMed          Journal:  JAMA Neurol        ISSN： 2168-6149            Impact factor:   18.302


× No keyword cloud information.
  2 in total

1.  Validation of Fragile X Screening in the Newborn Population Using a Fit-for-Purpose FMR1 PCR Assay System.

Authors:  Stacey Lee; Jennifer L Taylor; Charles Redmond; Andrew G Hadd; Jon A Kemppainen; Brian C Haynes; Scott Shone; Donald B Bailey; Gary J Latham
Journal:  J Mol Diagn       Date:  2019-12-19       Impact factor: 5.568

Review 2.  Fragile X syndrome: a review of clinical and molecular diagnoses.

Authors:  Claudia Ciaccio; Laura Fontana; Donatella Milani; Silvia Tabano; Monica Miozzo; Susanna Esposito
Journal:  Ital J Pediatr       Date:  2017-04-19       Impact factor: 2.638
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.