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Evidence for a Turner syndrome locus or loci at Xp11.2-p22.1.
Zinn AR, Tonk VS, Chen Z, Flejter WL, Gardner HA, Guerra R, Kushner H, Schwartz S, Sybert VP, Van Dyke DL, Ross JL. Zinn AR, et al. Among authors: ross jl. Am J Hum Genet. 1998 Dec;63(6):1757-66. doi: 10.1086/302152. Am J Hum Genet. 1998. PMID: 9837829 Free PMC article.
Turner syndrome and haploinsufficiency.
Zinn AR, Ross JL. Zinn AR, et al. Among authors: ross jl. Curr Opin Genet Dev. 1998 Jun;8(3):322-7. doi: 10.1016/s0959-437x(98)80089-0. Curr Opin Genet Dev. 1998. PMID: 9690998 Review.
Complete SHOX deficiency causes Langer mesomelic dysplasia.
Zinn AR, Wei F, Zhang L, Elder FF, Scott CI Jr, Marttila P, Ross JL. Zinn AR, et al. Among authors: ross jl. Am J Med Genet. 2002 Jun 15;110(2):158-63. doi: 10.1002/ajmg.10422. Am J Med Genet. 2002. PMID: 12116254
A Turner syndrome neurocognitive phenotype maps to Xp22.3.
Zinn AR, Roeltgen D, Stefanatos G, Ramos P, Elder FF, Kushner H, Kowal K, Ross JL. Zinn AR, et al. Among authors: ross jl. Behav Brain Funct. 2007 May 21;3:24. doi: 10.1186/1744-9081-3-24. Behav Brain Funct. 2007. PMID: 17517138 Free PMC article.
387 results