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Allan-Herndon-Dudley syndrome with unusual profound sensorineural hearing loss.
Am J Med Genet A. 2015 Aug;167A(8):1872-6. doi: 10.1002/ajmg.a.37075. Epub 2015 Apr 6.
Am J Med Genet A. 2015.
PMID: 25850411
Ectrodactyly and Lethal Pulmonary Acinar Dysplasia Associated with Homozygous FGFR2 Mutations Identified by Exome Sequencing.
Barnett CP, Nataren NJ, Klingler-Hoffmann M, Schwarz Q, Chong CE, Lee YK, Bruno DL, Lipsett J, McPhee AJ, Schreiber AW, Feng J, Hahn CN, Scott HS.
Barnett CP, et al.
Hum Mutat. 2016 Sep;37(9):955-63. doi: 10.1002/humu.23032. Epub 2016 Jul 11.
Hum Mutat. 2016.
PMID: 27323706
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Integrative genomic analysis reveals cancer-associated mutations at diagnosis of CML in patients with high-risk disease.
Branford S, Wang P, Yeung DT, Thomson D, Purins A, Wadham C, Shahrin NH, Marum JE, Nataren N, Parker WT, Geoghegan J, Feng J, Shanmuganathan N, Mueller MC, Dietz C, Stangl D, Donaldson Z, Altamura H, Georgievski J, Braley J, Brown A, Hahn C, Walker I, Kim SH, Choi SY, Park SH, Kim DW, White DL, Yong ASM, Ross DM, Scott HS, Schreiber AW, Hughes TP.
Branford S, et al.
Blood. 2018 Aug 30;132(9):948-961. doi: 10.1182/blood-2018-02-832253. Epub 2018 Jul 2.
Blood. 2018.
PMID: 29967129
Free article.
Clinical Trial.
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Molecular Skin Cancer Diagnosis: Promise and Limitations.
Nataren N, Yamada M, Prow T.
Nataren N, et al.
J Mol Diagn. 2023 Jan;25(1):17-35. doi: 10.1016/j.jmoldx.2022.09.008. Epub 2022 Oct 13.
J Mol Diagn. 2023.
PMID: 36243291
Free article.
Review.
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