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Polymicrogyria in a 10-month-old boy with Mowat-Wilson syndrome.
Am J Med Genet A. 2015 Oct;167A(10):2402-5. doi: 10.1002/ajmg.a.37171. Epub 2015 May 26.
Am J Med Genet A. 2015.
PMID: 26012591
Mosaic trisomy 15 in a liveborn infant.
McPadden J, Helm BM, Spangler BB, Ross LP, Boles DB, Schrier Vergano SA.
McPadden J, et al. Among authors: spangler bb.
Am J Med Genet A. 2015 Apr;167A(4):821-5. doi: 10.1002/ajmg.a.36958. Epub 2015 Mar 3.
Am J Med Genet A. 2015.
PMID: 25736076
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Three clinical experiences with SNP array results consistent with parental incest: a narrative with lessons learned.
Helm BM, Langley K, Spangler B, Vergano S.
Helm BM, et al.
J Genet Couns. 2014 Aug;23(4):489-95. doi: 10.1007/s10897-013-9669-0. Epub 2013 Nov 13.
J Genet Couns. 2014.
PMID: 24222483
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Military Health Care Dilemmas and Genetic Discrimination: A Family's Experience with Whole Exome Sequencing.
Helm BM, Langley K, Spangler BB, Schrier Vergano SA.
Helm BM, et al. Among authors: spangler bb.
Narrat Inq Bioeth. 2015 Summer;5(2):179-86. doi: 10.1353/nib.2015.0059.
Narrat Inq Bioeth. 2015.
PMID: 26300150
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Association of the missense variant p.Arg203Trp in PACS1 as a cause of intellectual disability and seizures.
Stern D, Cho MT, Chikarmane R, Willaert R, Retterer K, Kendall F, Deardorff M, Hopkins S, Bedoukian E, Slavotinek A, Schrier Vergano S, Spangler B, McDonald M, McConkie-Rosell A, Burton BK, Kim KH, Oundjian N, Kronn D, Chandy N, Baskin B, Guillen Sacoto MJ, Wentzensen IM, McLaughlin HM, McKnight D, Chung WK.
Stern D, et al.
Clin Genet. 2017 Aug;92(2):221-223. doi: 10.1111/cge.12956. Epub 2017 Jan 23.
Clin Genet. 2017.
PMID: 28111752
Free PMC article.
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