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kylie williams
(57 results)?
Genetics of Congenital Heart Disease.
Biomolecules. 2019 Dec 16;9(12):879. doi: 10.3390/biom9120879.
Biomolecules. 2019.
PMID: 31888141
Free PMC article.
Review.
Rare and Common Variants Uncover the Role of the Atria in Coarctation of the Aorta.
Zhu W, Williams K, Young C, Lin JH, Teekakirikul P, Lo CW.
Zhu W, et al. Among authors: williams k.
Genes (Basel). 2022 Apr 2;13(4):636. doi: 10.3390/genes13040636.
Genes (Basel). 2022.
PMID: 35456442
Free PMC article.
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Contribution of LRP1 in Human Congenital Heart Disease Correlates with Its Roles in the Outflow Tract and Atrioventricular Cushion Development.
Arrigo AB, Zhu W, Williams KA, Guzman-Moreno C, Lo C, Lin JI.
Arrigo AB, et al. Among authors: williams ka.
Genes (Basel). 2023 Apr 21;14(4):947. doi: 10.3390/genes14040947.
Genes (Basel). 2023.
PMID: 37107705
Free PMC article.
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Common deletion variants causing protocadherin-α deficiency contribute to the complex genetics of BAV and left-sided congenital heart disease.
Teekakirikul P, Zhu W, Gabriel GC, Young CB, Williams K, Martin LJ, Hill JC, Richards T, Billaud M, Phillippi JA, Wang J, Wu Y, Tan T, Devine W, Lin JH, Bais AS, Klonowski J, Moreau de Bellaing A, Saini A, Wang MX, Emerel L, Salamacha N, Wyman SK, Lee C, Sing Li H, Miron A, Zhang J, Xing J, McNamara DM, Fung E, Kirshbom P, Mahle W, Kochilas LK, He Y, Garg V, White P, McBride KL, Benson DW, Gleason TG, Mital S, Lo CW.
Teekakirikul P, et al. Among authors: williams k.
HGG Adv. 2021 Jul 8;2(3):100037. doi: 10.1016/j.xhgg.2021.100037. Epub 2021 Jul 29.
HGG Adv. 2021.
PMID: 34888534
Free PMC article.
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