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Gordon, Derek; Zinn, Andrew R (2009) Computing power of quantitative trait locus association mapping for haploid loci. BMC Bioinformatics 10:261
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Zinn, Andrew R; Kushner, Harvey; Ross, Judith L (2008) EFHC2 SNP rs7055196 is not associated with fear recognition in 45,X Turner syndrome. Am J Med Genet B Neuropsychiatr Genet 147B:507-9
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Simon, T J; Takarae, Y; DeBoer, T et al. (2008) Overlapping numerical cognition impairments in children with chromosome 22q11.2 deletion or Turner syndromes. Neuropsychologia 46:82-94
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Campos-Barros, Angel; Benito-Sanz, Sara; Ross, Judith L et al. (2007) Compound heterozygosity of SHOX-encompassing and downstream PAR1 deletions results in Langer mesomelic dysplasia (LMD). Am J Med Genet A 143A:933-8
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Bondy, Carolyn A; Matura, Lea Ann; Wooten, Nicole et al. (2007) The physical phenotype of girls and women with Turner syndrome is not X-imprinted. Hum Genet 121:469-74
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Russell, Heather F; Wallis, Deeann; Mazzocco, Michele M M et al. (2006) Increased prevalence of ADHD in Turner syndrome with no evidence of imprinting effects. J Pediatr Psychol 31:945-55
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Van, Phillip L; Bakalov, Vladimir K; Zinn, Andrew R et al. (2006) Maternal X chromosome, visceral adiposity, and lipid profile. JAMA 295:1373-4
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Zinn, Andrew R; Ramos, Purita; Ross, Judith L (2006) A second recombination hotspot associated with SHOX deletions. Am J Hum Genet 78:523-5
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Ross, Judith L; Kowal, Karen; Quigley, Charmian A et al. (2005) The phenotype of short stature homeobox gene (SHOX) deficiency in childhood: contrasting children with Leri-Weill dyschondrosteosis and Turner syndrome. J Pediatr 147:499-507
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Boycott, Kym M; Parslow, Malcolm I; Ross, Judith L et al. (2003) A familial contiguous gene deletion syndrome at Xp22.3 characterized by severe learning disabilities and ADHD. Am J Med Genet A 122A:139-47
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Showing the most recent 10 out of 22 publications
