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Extension of the mutational and clinical spectrum of SOX2 related disorders: Description of six new cases and a novel association with suprasellar teratoma.
Am J Med Genet A. 2018 Dec;176(12):2710-2719. doi: 10.1002/ajmg.a.40644. Epub 2018 Nov 18.
Am J Med Genet A. 2018.
PMID: 30450772
Isolated vocal cord paralysis in two siblings with compound heterozygous variants in MUSK: Expanding the phenotypic spectrum.
Murali C, Li D, Grand K, Hakonarson H, Bhoj E.
Murali C, et al.
Am J Med Genet A. 2019 Apr;179(4):655-658. doi: 10.1002/ajmg.a.61060. Epub 2019 Feb 4.
Am J Med Genet A. 2019.
PMID: 30719842
Free PMC article.
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