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Endocrinology|May 20, 2006
SIM1 overexpression partially rescues agouti yellow and diet-induced obesity by normalizing food intakeBassil M Kublaoui, J Lloyd Holder, Kristen P Tolson, et al.American Journal of Medical Genetics. Part A|December 12, 2002
Mesomelic and rhizomelic short stature: The phenotype of combined Leri-Weill dyschondrosteosis and achondroplasia or hypochondroplasiaJudith L Ross, Gary Bellus, Charles I Scott, et al.American Journal of Medical Genetics. Part A|March 31, 2007
Compound heterozygosity of SHOX-encompassing and downstream PAR1 deletions results in Langer mesomelic dysplasia (LMD)Angel Campos-Barros, Sara Benito-Sanz, Judith L Ross, et al.Journal of Pediatric Surgery|November 21, 2007
Phenotypic expansion of the supernumerary derivative (22) chromosome syndrome: VACTERL and Hirschsprung's diseaseJuan C Prieto, Nilda M Garcia, Frederick F Elder, et al.Developmental Disabilities Research Reviews|December 17, 2009
An extra X or Y chromosome: contrasting the cognitive and motor phenotypes in childhood in boys with 47,XYY syndrome or 47,XXY Klinefelter syndromeJudith L Ross, Martha P D Zeger, Harvey Kushner, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 12, 2010
Postnatal Sim1 deficiency causes hyperphagic obesity and reduced Mc4r and oxytocin expressionKristen P Tolson, Terry Gemelli, Laurent Gautron, et al.The Journal of Clinical Endocrinology and Metabolism|June 16, 2005
Androgen receptor CAGn repeat length influences phenotype of 47,XXY (Klinefelter) syndromeAndrew R Zinn, Purita Ramos, Frederick F Elder, et al.Human Genetics|January 24, 2007
The physical phenotype of girls and women with Turner syndrome is not X-imprintedCarolyn A Bondy, Lea Ann Matura, Nicole Wooten, et al.Molecular Cytogenetics|February 17, 2009
MODY-like diabetes associated with an apparently balanced translocation: possible involvement of MPP7 gene and cell polarity in the pathogenesis of diabetesElizabeth J Bhoj, Stefano Romeo, Marco G Baroni, et al.American Journal of Medical Genetics|July 13, 2002
Complete SHOX deficiency causes Langer mesomelic dysplasiaAndrew R Zinn, Fanglin Wei, Ling Zhang, et al.Pageof 5