Unconventional Wisdom About the Obesity EpidemicZINN, Andrew R.The American journal of the medical sciences (Print). 2010, Vol 340, Num 6, pp 481-491, issn 0002-9629, 11 p.Article

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

Human balanced translocation and mouse gene inactivation implicate Basonuclin 2 in distal urethral developmentBHOJ, Elizabeth J; RAMOS, Purita; VANHOUTTEGHEM, Amandine et al.European journal of human genetics. 2011, Vol 19, Num 5, pp 540-546, issn 1018-4813, 7 p.Article

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

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

UBE2A Deficiency Syndrome: Mild to Severe Intellectual Disability Accompanied by Seizures, Absent Speech, Urogenital, and Skin Anomalies in Male PatientsDE LEEUW, Nicole; BULK, Saskia; VAN BOKHOVEN, Hans et al.American journal of medical genetics. Part A. 2010, Vol 152, Num 12, pp 3084-3090, issn 1552-4825, 7 p.Article

Cryptic Chromosomal Abnormalities Identified in Children With Congenital Heart DiseaseRICHARDS, Ashleigh A; JAECKLE SANTOS, Lane; NICHOLS, Haley A et al.Pediatric research. 2008, Vol 64, Num 4, pp 358-363, issn 0031-3998, 6 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

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

Refined mapping of X-linked reticulate pigmentary disorder and sequencing of candidate genesJAECKLE SANTOS, Lane J; CHAO XING; SHOUBRIDGE, Cheryl et al.Human genetics. 2008, Vol 123, Num 5, pp 469-476, issn 0340-6717, 8 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 Growth Hormone Therapy on Severe Short Stature and Skeletal Deformities in a Patient with Combined Turner Syndrome and Langer Mesomelic DysplasiaSHAH, Bina C; MORAN, Ellen S; ZINN, Andrew R et al.The Journal of clinical endocrinology and metabolism. 2009, Vol 94, Num 12, pp 5028-5033, issn 0021-972X, 6 p.Article

The physical phenotype of girls and women with Turner syndrome is not X-imprintedBONDY, Carolyn A; MATURA, Lea Ann; WOOTEN, Nicole et al.Human genetics. 2007, Vol 121, Num 3-4, pp 469-474, issn 0340-6717, 6 p.Article

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

Sim1 gene dosage modulates the homeostatic feeding response to increased dietary fat in miceHOLDER, J. Lloyd; LING ZHANG; KUBLAOUI, Bassil M et al.American journal of physiology. Endocrinology and metabolism. 2004, Vol 50, Num 1, pp E105-E113, issn 0193-1849Article

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