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. …
Young Lab
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 …
Identification of a novel locus on 2q for autosomal dominant high-grade myopia.
PubMed ID: 15980214 Author(s): Paluru PC, Nallasamy S, Devoto M, Rappaport EF, Young TL. Identification of a novel locus on 2q for autosomal dominant high-grade myopia. Invest Ophthalmol Vis Sci. 2005 Jul;46(7):2300-7. PMID 15980214 Journal: …
Evaluation of Lipin 2 as a candidate gene for autosomal dominant 1 high-grade myopia.
PubMed ID: 15862761 Author(s): Zhou J, Young TL. Evaluation of Lipin 2 as a candidate gene for autosomal dominant 1 high-grade myopia. Gene. 2005 Jun 6;352:10-9. PMID 15862761 Journal: Gene, Volume 352, Jun 2005 The …
Familial variable expression of dilated cardiomyopathy in Alström syndrome: a report of four sibs.
PubMed ID: 15809999 Author(s): Hoffman JD, Jacobson Z, Young TL, Marshall JD, Kaplan P. Familial variable expression of dilated cardiomyopathy in Alström syndrome: a report of four sibs. Am J Med Genet A. 2005 May …
The association of astigmatism and spherical refractive error in a high myopia cohort.
PubMed ID: 15829852 Author(s): Heidary G, Ying GS, Maguire MG, Young TL. The association of astigmatism and spherical refractive error in a high myopia cohort. Optom Vis Sci. 2005 Apr;82(4):244-7. PMID 15829852 Journal: Optometry And …
Subtelomeric deletions of chromosome 6p: molecular and cytogenetic characterization of three new cases with phenotypic overlap with Ritscher-Schinzel (3C) syndrome.
PubMed ID: 15704124 Author(s): Descipio C, Schneider L, Young TL, Wasserman N, Yaeger D, Lu F, Wheeler PG, Williams MS, Bason L, Jukofsky L, Menon A, Geschwindt R, Chudley AE, Saraiva J, Schinzel AA, Guichet …