Literature DB >> 25061175

Misleading results from saliva samples of patients post-BMT in exome analyses.

C Alexander Valencia1, Subba Rao Indugula1, Abhinav Mathur1, Chao Wei1, Jenice Caitlin Brown1, India Cole1, Sarah Dell1, Jessica Connor1, Kejian Zhang1.   

Abstract

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Year:  2014        PMID： 25061175     DOI： 10.1182/blood-2014-04-572941

Source DB:  PubMed          Journal:  Blood        ISSN： 0006-4971            Impact factor:   22.113


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  3 in total

1.  Challenges in returning results in a genomic medicine implementation study: the Return of Actionable Variants Empirical (RAVE) study.

Authors:  David C Kochan; Erin Winkler; Noralane Lindor; Gabriel Q Shaibi; Janet Olson; Pedro J Caraballo; Robert Freimuth; Joel E Pacyna; Carmen Radecki Breitkopf; Richard R Sharp; Iftikhar J Kullo
Journal:  NPJ Genom Med       Date:  2020-05-04       Impact factor: 8.617

2.  Inherited CHST11/MIR3922 deletion is associated with a novel recessive syndrome presenting with skeletal malformation and malignant lymphoproliferative disease.

Authors:  Sameer S Chopra; Ignaty Leshchiner; Hatice Duzkale; Heather McLaughlin; Monica Giovanni; Chengsheng Zhang; Nathan Stitziel; Joyce Fingeroth; Robin M Joyce; Matthew Lebo; Heidi Rehm; Dana Vuzman; Richard Maas; Shamil R Sunyaev; Michael Murray; Christopher A Cassa
Journal:  Mol Genet Genomic Med       Date:  2015-05-10       Impact factor: 2.183

3.  Challenges in returning results in a genomic medicine implementation study: the Return of Actionable Variants Empirical (RAVE) study.

Authors:  David C Kochan; Erin Winkler; Noralane Lindor; Gabriel Q Shaibi; Janet Olson; Pedro J Caraballo; Robert Freimuth; Joel E Pacyna; Carmen Radecki Breitkopf; Richard R Sharp; Iftikhar J Kullo
Journal:  NPJ Genom Med       Date:  2020-05-04       Impact factor: 8.617
  3 in total

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