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MESP1 Mutations in Patients with Congenital Heart Defects.
Hum Mutat. 2016 Mar;37(3):308-14. doi: 10.1002/humu.22947. Epub 2016 Jan 19.
Hum Mutat. 2016.
PMID: 26694203
Free PMC article.
Analysis of chromosomal structural variation in patients with congenital left-sided cardiac lesions.
White PS, Xie HM, Werner P, Glessner J, Latney B, Hakonarson H, Goldmuntz E.
White PS, et al. Among authors: latney b.
Birth Defects Res A Clin Mol Teratol. 2014 Dec;100(12):951-64. doi: 10.1002/bdra.23279. Epub 2014 Jul 26.
Birth Defects Res A Clin Mol Teratol. 2014.
PMID: 25066379
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Mutations in NTRK3 suggest a novel signaling pathway in human congenital heart disease.
Werner P, Paluru P, Simpson AM, Latney B, Iyer R, Brodeur GM, Goldmuntz E.
Werner P, et al. Among authors: latney b.
Hum Mutat. 2014 Dec;35(12):1459-68. doi: 10.1002/humu.22688. Epub 2014 Nov 7.
Hum Mutat. 2014.
PMID: 25196463
Free PMC article.
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NKX2-6 related congenital heart disease: Biallelic homeodomain-disrupting variants and truncus arteriosus.
Ritter A, Werner P, Latney B, Krock BL, Santani A, Bedoukian E, Skraban CM, Deardorff MA, Goldmuntz E.
Ritter A, et al. Among authors: latney b.
Am J Med Genet A. 2020 Jun;182(6):1454-1459. doi: 10.1002/ajmg.a.61550. Epub 2020 Mar 21.
Am J Med Genet A. 2020.
PMID: 32198970
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The phenotypic spectrum of ZIC3 mutations includes isolated d-transposition of the great arteries and double outlet right ventricle.
D'Alessandro LC, Latney BC, Paluru PC, Goldmuntz E.
D'Alessandro LC, et al. Among authors: latney bc.
Am J Med Genet A. 2013 Apr;161A(4):792-802. doi: 10.1002/ajmg.a.35849. Epub 2013 Feb 20.
Am J Med Genet A. 2013.
PMID: 23427188
Free PMC article.
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