EFHC2 SNP rs7055196 Is Not Associated With Fear Recognition in 45,X Turner SyndromeZINN, Andrew R; KUSHNER, Harvey; ROSS, Judith L et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2008, Vol 147, Num 4, pp 507-509, issn 1552-4841, 3 p.Article

Psychosocial development in adolescents with Turner syndromeMCCAULEY, Elizabeth; FEUILLAN, Penelope; KUSHNER, Harvey et al.Journal of developmental and behavioral pediatrics. 2001, Vol 22, Num 6, pp 360-365, issn 0196-206XArticle

Increased prevalence of ADHD in turner syndrome with no evidence of imprinting effectsRUSSELL, Heather F; WALLIS, Deeann; MAZZOCCO, Michèle M. M et al.Journal of pediatric psychology. 2006, Vol 31, Num 9, pp 945-955, issn 0146-8693, 11 p.Article

Complete SHOX deficiency causes Langer mesomelic dysplasiaZINN, Andrew R; FANGLIN WEI; LING ZHANG et al.American journal of medical genetics. 2002, Vol 110, Num 2, pp 158-163, issn 0148-7299Article

Behavioral and Social Phenotypes in Boys With 47,XYY Syndrome or 47,XXY Klinefelter SyndromeROSS, Judith L; ROELTGEN, David P; KUSHNER, Harvey et al.Pediatrics (Evanston). 2012, Vol 129, Num 4, pp 769-778, issn 0031-4005, 10 p.Article

The phenotype of short stature homeobox gene (SHOX) deficiency in childhood : Contrasting children with leri-weill dyschondrosteosis and turner syndromeROSS, Judith L; KOWAL, Karen; QUIGLEY, Charmian A et al.The Journal of pediatrics. 2005, Vol 147, Num 4, pp 499-507, issn 0022-3476, 9 p.Article

A man who inherited his SRY gene and Leri-Weill dyschondrosteosis from his mother and neurofibromatosis type 1 from his fatherFANGLIN WEI; SOU CHENG; BADIE, Nicole et al.American journal of medical genetics. 2001, Vol 102, Num 4, pp 353-358, issn 0148-7299Article

Effect of Ascertainment and Genetic Features on the Phenotype of Klinefelter SyndromeZEGER, Martha P. D; ZINN, Andrew R; LAHLOU, Najiba et al.The Journal of pediatrics. 2008, Vol 152, Num 5, pp 716-722, issn 0022-3476, 7 p.Article

Differences in follicle-stimulating hormone secretion between 45,X monosomy turner syndrome and 45,X/46,XX mosaicism are evident at an early ageFECHNER, Patricia Y; DAVENPORT, Marsha L; QUALY, Rebecca L et al.The Journal of clinical endocrinology and metabolism. 2006, Vol 91, Num 12, pp 4896-4902, issn 0021-972X, 7 p.Article

Language use in females with fragile X or turner syndrome during brief initial social interactionsMAZZOCCO, Michele M. M; THOMPSON, Laurie; SUDHALTER, Vicki et al.Journal of developmental and behavioral pediatrics. 2006, Vol 27, Num 4, pp 319-328, issn 0196-206X, 10 p.Article

A familial contiguous gene deletion syndrome at Xp22.3 characterized by severe learning disabilities and ADHDBOYCOTT, Kym M; PARSLOW, Malcolm I; ROSS, Judith L et al.American journal of medical genetics. 2003, Vol 122A, Num 2, pp 139-147, issn 0148-7299, 9 p.Article

Brain development in Turner syndrome: a magnetic resonance imaging studyBROWN, Wendy E; KESLER, Shelli R; REISS, Allan L et al.Psychiatry research. Neuroimaging. 2002, Vol 116, Num 3, pp 187-196, issn 0925-4927, 10 p.Article

Molecular analysis of genes on Xp controlling Turner syndrome and premature ovarian failure (POF)ZINN, Andrew R; ROSS, Judith L.Seminars in reproductive medicine. 2001, Vol 19, Num 2, pp 141-146Article

A Multicenter, Open-Label, Observational Study of Testosterone Gel (1%) in the Treatment of Adolescent Boys With Klinefelter Syndrome or AnorchiaROGOL, Alan D; SWERDLOFF, Ronald S; REITER, Edward O et al.Journal of adolescent health. 2014, Vol 54, Num 1, pp 20-25, issn 1054-139X, 6 p.Article

C-Type Natriuretic Peptide (CNP) Levels Are Altered in Boys with Klinefelter SyndromeOLNEY, Robert C; PRICKETT, Timothy C. R; ESPINER, Eric A et al.The Journal of clinical endocrinology and metabolism. 2012, Vol 97, Num 11, pp 4206-4211, issn 0021-972X, 6 p.Article

Atypical Functional Brain Activation During a Multiple Object Tracking Task in Girls With Turner Syndrome: Neurocorrelates of Reduced Spatiotemporal ResolutionBEATON, Elliott A; STODDARD, Joel; SONG LAI et al.American journal on intellectual and developmental disabilities (Print). 2010, Vol 115, Num 2, issn 1944-7515, 140-156, 191 [18 p.]Article

Compound heterozygosity of SHOX-encompassing and downstream PAR1 deletions results in langer mesomelic dysplasia (LMD)CAMPOS-BARROS, Angel; BENITO-SANZ, Sara; ROSS, Judith L et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 9, pp 933-938, issn 1552-4825, 6 p.Article

Growth hormone is effective in treatment of short stature associated with short stature homeobox-containing gene deficiency : Two-year results of a randomized, controlled, multicenter trialBLUM, Werner F; CROWE, Brenda J; QUIGLEY, Charmian A et al.The Journal of clinical endocrinology and metabolism. 2007, Vol 92, Num 1, pp 219-228, issn 0021-972X, 10 p.Article

Hypodense nodularity on computed tomography: Novel imaging and pathology of micronodular adrenocortical hyperplasia associated with myelolipomatous changesCOURCOUTSAKIS, Nickolas A; PATRONAS, Nickolas J; CASSARINO, David et al.The Journal of clinical endocrinology and metabolism. 2004, Vol 89, Num 8, pp 3737-3738, issn 0021-972X, 2 p.Article