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Adaptation and validation of the ACMG/AMP variant classification framework for MYH7-associated inherited cardiomyopathies: recommendations by ClinGen's Inherited Cardiomyopathy Expert Panel.
Genet Med. 2018 Mar;20(3):351-359. doi: 10.1038/gim.2017.218. Epub 2018 Jan 4.
Genet Med. 2018.
PMID: 29300372
Free PMC article.
ClinGen's RASopathy Expert Panel consensus methods for variant interpretation.
Gelb BD, Cavé H, Dillon MW, Gripp KW, Lee JA, Mason-Suares H, Rauen KA, Williams B, Zenker M, Vincent LM; ClinGen RASopathy Working Group.
Gelb BD, et al. Among authors: dillon mw.
Genet Med. 2018 Nov;20(11):1334-1345. doi: 10.1038/gim.2018.3. Epub 2018 Mar 1.
Genet Med. 2018.
PMID: 29493581
Free PMC article.
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Assessing the gene-disease association of 19 genes with the RASopathies using the ClinGen gene curation framework.
Grant AR, Cushman BJ, Cavé H, Dillon MW, Gelb BD, Gripp KW, Lee JA, Mason-Suares H, Rauen KA, Tartaglia M, Vincent LM, Zenker M.
Grant AR, et al. Among authors: dillon mw.
Hum Mutat. 2018 Nov;39(11):1485-1493. doi: 10.1002/humu.23624.
Hum Mutat. 2018.
PMID: 30311384
Free PMC article.
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Expanding the Noonan spectrum/RASopathy NGS panel: Benefits of adding NF1 and SPRED1.
Witkowski L, Dillon MW, Murphy E, S Lebo M, Mason-Suares H.
Witkowski L, et al. Among authors: dillon mw.
Mol Genet Genomic Med. 2020 Apr;8(4):e1180. doi: 10.1002/mgg3.1180. Epub 2020 Feb 27.
Mol Genet Genomic Med. 2020.
PMID: 32107864
Free PMC article.
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Retrospective study of prenatal ultrasound findings in newborns with a Noonan spectrum disorder.
Hakami F, Dillon MW, Lebo M, Mason-Suares H.
Hakami F, et al. Among authors: dillon mw.
Prenat Diagn. 2016 May;36(5):418-23. doi: 10.1002/pd.4797. Epub 2016 Mar 28.
Prenat Diagn. 2016.
PMID: 26918529
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Lessons learned from expanded reproductive carrier screening in self-reported Ashkenazi, Sephardi, and Mizrahi Jewish patients.
Akler G, Birch AH, Schreiber-Agus N, Cai X, Cai G, Shi L, Yu C, Larmore AM, Mendiratta-Vij G, Elkhoury L, Dillon MW, Zhu J, Mclellan AS, Suer FE, Webb BD, Schadt EE, Kornreich R, Edelmann L.
Akler G, et al. Among authors: dillon mw.
Mol Genet Genomic Med. 2020 Feb;8(2):e1053. doi: 10.1002/mgg3.1053. Epub 2019 Dec 27.
Mol Genet Genomic Med. 2020.
PMID: 31880409
Free PMC article.
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RAF1-associated Noonan syndrome presenting antenatally with an abnormality of skull shape, subdural haematoma and associated with novel cerebral malformations.
Hartill VL, Dillon MW, Warren DJ, Blyth M.
Hartill VL, et al. Among authors: dillon mw.
Clin Dysmorphol. 2017 Apr;26(2):101-106. doi: 10.1097/MCD.0000000000000153.
Clin Dysmorphol. 2017.
PMID: 27753652
No abstract available.
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Clinical Pharmacogenetic Testing and the Posttest Counseling Conundrum.
Rigobello R, Rahawi S, Wallsten R, Cody N, Nicoletti P, Owusu Obeng A, Naik H, Dillon MW, Scott SA.
Rigobello R, et al. Among authors: dillon mw.
Clin Pharmacol Ther. 2020 Nov;108(5):924-928. doi: 10.1002/cpt.1913. Epub 2020 Jun 27.
Clin Pharmacol Ther. 2020.
PMID: 32592592
No abstract available.
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