PubMed ID: 17210850 Author(s): Young TL, Metlapally R, Shay AE. Complex trait genetics of refractive error. Arch Ophthalmol. 2007 Jan;125(1):38-48. Review. PMID 17210850 Journal: Archives Of Ophthalmology (Chicago, Ill. : 1960), Volume 125, Issue 1, …
Young Lab
Ocular abnormalities in Apert syndrome: genotype/phenotype correlations with fibroblast growth factor receptor type 2 mutations.
PubMed ID: 17189145 Author(s): Jadico SK, Young DA, Huebner A, Edmond JC, Pollock AN, McDonald-McGinn DM, Li YJ, Zackai EH, Young TL. Ocular abnormalities in Apert syndrome: genotype/phenotype correlations with fibroblast growth factor receptor type …
Ocular phenotype correlations in patients with TWIST versus FGFR3 genetic mutations.
PubMed ID: 17070479 Author(s): Jadico SK, Huebner A, McDonald-McGinn DM, Zackai EH, Young TL. Ocular phenotype correlations in patients with TWIST versus FGFR3 genetic mutations. J AAPOS. 2006 Oct;10(5):435-44. PMID 17070479 Journal: Journal Of Aapos …
Small leucine rich repeat proteoglycans (SLRPs) in the human sclera: identification of abundant levels of PRELP.
PubMed ID: 17093390 Author(s): Johnson JM, Young TL, Rada JA. Small leucine rich repeat proteoglycans (SLRPs) in the human sclera: identification of abundant levels of PRELP. Mol Vis. 2006 Sep 13;12:1057-66. PMID 17093390 Journal: Molecular …
Differential gene expression in mouse sclera during ocular development.
PubMed ID: 16638983 Author(s): Zhou J, Rappaport EF, Tobias JW, Young TL. Differential gene expression in mouse sclera during ocular development. Invest Ophthalmol Vis Sci. 2006 May;47(5):1794-802. PMID 16638983 Journal: Investigative Ophthalmology & Visual Science, …
Ophthalmologic findings in Cornelia de Lange syndrome: a genotype-phenotype correlation study.
PubMed ID: 16606884 Author(s): Nallasamy S, Kherani F, Yaeger D, McCallum J, Kaur M, Devoto M, Jackson LG, Krantz ID, Young TL. Ophthalmologic findings in Cornelia de Lange syndrome: a genotype-phenotype correlation study. Arch Ophthalmol. …
The natural history of glaucoma and ocular hypertension after pediatric cataract surgery.
PubMed ID: 16527681 Author(s): Egbert JE, Christiansen SP, Wright MM, Young TL, Summers CG. The natural history of glaucoma and ocular hypertension after pediatric cataract surgery. J AAPOS. 2006 Feb;10(1):54-7. PMID 16527681 Journal: Journal Of …
Two novel TP63 mutations associated with the ankyloblepharon, ectodermal defects, and cleft lip and palate syndrome: a skin fragility phenotype.
PubMed ID: 16365259 Author(s): Payne AS, Yan AC, Ilyas E, Li W, Seykora JT, Young TL, Pawel BR, Honig PJ, Camacho J, Imaizumi S, Heymann WR, Schnur RE. Two novel TP63 mutations associated with the …
Norrie disease gene sequence variants in an ethnically diverse population with retinopathy of prematurity.
PubMed ID: 16052165 Author(s): Hutcheson KA, Paluru PC, Bernstein SL, Koh J, Rappaport EF, Leach RA, Young TL. Norrie disease gene sequence variants in an ethnically diverse population with retinopathy of prematurity. Mol Vis. 2005 …