Bain NL[au] - Search Results

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Year	Number of Results
2013	1
2014	2
2015	2
2022	0

Page 1

16p13.11 microdeletion in a patient with hemiconvulsion-hemiplegia-epilepsy syndrome: a case report.

Miteff CI, Smith RL, Bain NL, Subramanian G, Brown JE, Kamien B. Miteff CI, et al. Among authors: bain nl. J Child Neurol. 2015 Jan;30(1):83-6. doi: 10.1177/0883073813516382. Epub 2014 Jan 21. J Child Neurol. 2015. PMID: 24453159

Copy number variants in patients with intellectual disability affect the regulation of ARX transcription factor gene.

Ishibashi M, Manning E, Shoubridge C, Krecsmarik M, Hawkins TA, Giacomotto J, Zhao T, Mueller T, Bader PI, Cheung SW, Stankiewicz P, Bain NL, Hackett A, Reddy CC, Mechaly AS, Peers B, Wilson SW, Lenhard B, Bally-Cuif L, Gecz J, Becker TS, Rinkwitz S. Ishibashi M, et al. Among authors: bain nl. Hum Genet. 2015 Nov;134(11-12):1163-82. doi: 10.1007/s00439-015-1594-x. Epub 2015 Sep 4. Hum Genet. 2015. PMID: 26337422

Genomic profiling of plasma cell disorders in a clinical setting: integration of microarray and FISH, after CD138 selection of bone marrow.

Berry NK, Bain NL, Enjeti AK, Rowlings P. Berry NK, et al. Among authors: bain nl. J Clin Pathol. 2014 Jan;67(1):66-9. doi: 10.1136/jclinpath-2013-201691. Epub 2013 Aug 22. J Clin Pathol. 2014. PMID: 23969274 Free PMC article.

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