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A homozygous POC1B variant causes recessive cone-rod dystrophy.
Ophthalmic Genet. 2021 Jun;42(3):349-353. doi: 10.1080/13816810.2021.1894460. Epub 2021 Mar 4.
Ophthalmic Genet. 2021.
PMID: 33657974
The Axenfeld-Rieger Syndrome Gene FOXC1 Contributes to Left-Right Patterning.
Chrystal PW, French CR, Jean F, Havrylov S, van Baarle S, Peturson AM, Xu P, Crump JG, Pilgrim DB, Lehmann OJ, Waskiewicz AJ.
Chrystal PW, et al. Among authors: peturson am.
Genes (Basel). 2021 Jan 26;12(2):170. doi: 10.3390/genes12020170.
Genes (Basel). 2021.
PMID: 33530637
Free PMC article.
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Sickle cell trait newborn screen results: disclosure and management.
Lilley M, Hoang S, Blumenschein P, Peturson AM, Sosova I, Macneil L, Ridsdale R, Christian S.
Lilley M, et al. Among authors: peturson am.
J Community Genet. 2021 Jan;12(1):137-142. doi: 10.1007/s12687-020-00489-x. Epub 2020 Oct 26.
J Community Genet. 2021.
PMID: 33106985
Free PMC article.
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