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Year | Number of Results |
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2009 | 1 |
2021 | 2 |
2022 | 1 |
2024 | 0 |
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Page 1
Atypical aplasia cutis in association with Xia Gibbs syndrome.
Pediatr Dermatol. 2021 Mar;38(2):533-535. doi: 10.1111/pde.14515. Epub 2021 Jan 19.
Pediatr Dermatol. 2021.
PMID: 33464633
Inherited Retinal Dystrophy in Southeastern United States: Characterization of South Carolina Patients and Comparative Literature Review.
Griffith J 3rd, Sioufi K, Wilbanks L, Magrath GN, Say EAT, Lyons MJ, Wilkes M, Pai GS, Peterseim MMW.
Griffith J 3rd, et al. Among authors: pai gs.
Genes (Basel). 2022 Aug 20;13(8):1490. doi: 10.3390/genes13081490.
Genes (Basel). 2022.
PMID: 36011402
Free PMC article.
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Novel missense p.R252L mutation of ITGB4 compounded with known 3793+1G>A mutation associated with nonlethal epidermolysis bullosa-pyloric atresia with obstructive uropathy.
Ellis C, Eason C, Snyder A, Siegel M, Pai GS, Ryan E, Pfendner EG, Lee LW.
Ellis C, et al. Among authors: pai gs.
JAAD Case Rep. 2021 Mar 20;11:63-68. doi: 10.1016/j.jdcr.2021.03.016. eCollection 2021 May.
JAAD Case Rep. 2021.
PMID: 33937469
Free PMC article.
No abstract available.
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Incontinentia pigmenti with a foreshortened hand: evidence for the significance of NFkappaB in human morphogenesis.
Kmetz EC, Shashidhar Pai G, Burges GE.
Kmetz EC, et al. Among authors: shashidhar pai g.
Pediatr Dermatol. 2009 Jan-Feb;26(1):83-6. doi: 10.1111/j.1525-1470.2008.00829.x.
Pediatr Dermatol. 2009.
PMID: 19250414
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