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X-linked high myopia associated with cone dysfunction.
Young TL, Deeb SS, Ronan SM, Dewan AT, Alvear AB, Scavello GS, Paluru PC, Brott MS, Hayashi T, Holleschau AM, Benegas N, Schwartz M, Atwood LD, Oetting WS, Rosenberg T, Motulsky AG, King RA. Young TL, et al. Among authors: ronan sm. Arch Ophthalmol. 2004 Jun;122(6):897-908. doi: 10.1001/archopht.122.6.897. Arch Ophthalmol. 2004. PMID: 15197065
Evidence that a locus for familial high myopia maps to chromosome 18p.
Young TL, Ronan SM, Drahozal LA, Wildenberg SC, Alvear AB, Oetting WS, Atwood LD, Wilkin DJ, King RA. Young TL, et al. Among authors: ronan sm. Am J Hum Genet. 1998 Jul;63(1):109-19. doi: 10.1086/301907. Am J Hum Genet. 1998. PMID: 9634508 Free PMC article.
A second locus for familial high myopia maps to chromosome 12q.
Young TL, Ronan SM, Alvear AB, Wildenberg SC, Oetting WS, Atwood LD, Wilkin DJ, King RA. Young TL, et al. Among authors: ronan sm. Am J Hum Genet. 1998 Nov;63(5):1419-24. doi: 10.1086/302111. Am J Hum Genet. 1998. PMID: 9792869 Free PMC article.
13 results