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Related: Results 111 - 120 for Pendred's syndromeDFN8 - deafness, X-linked 8Novel syndrome of cataracts, retinitis pigmentosa, late onset deafness and sperm abnormalities: a new Usher syndrome subtype with X-linked inheritance? http://www.ihop-net.org/UniPub/iHOP/gs/87692.html open pop Pendragon, Uther definition of Pendragon, Uther in the Free Online ... Pendragon, Uther: see Arthurian legend Arthurian legend, the mass of legend, popular ... Pendred's Syndrome Pendred's Syndrome: Pendrell Pendrin Pendrive Pendrive Pendula http://encyclopedia2.thefreedictionary.com/Pendragon%2c+Uther open pop Co-expression of Pendrin, Vacuolar H+-ATPase {alpha}4-Subunit and ... Everett LA, Morsli H, Wu DK, Green ED (1999) Expression pattern of the mouse ortholog of the Pendred's syndrome gene (Pds) suggests a key role for pendrin in the inner ear. http://www.jhc.org/cgi/content/full/52/10/1377 open pop Identification of Pendrin as a Common Mediator for Mucus Production in ... Expression pattern of the mouse ortholog of the Pendred’s syndrome gene (Pds) suggests a key role for pendrin in the inner ear. Proc. Natl. Acad. http://www.jimmunol.org/cgi/content/full/180/9/6262 open pop Emergency Clinical Guide Presents Clinical Eponyms O-P Pendred’s syndrome ... Obesity hypoventilation syndrome defined by extreme obesity and alveolar ... http://www.anisman.com/ecg/eponymsop.htm open pop Goiter and thyroid cancer in children Expression pattern of the mouse ortholog of the Pendred's syndrome gene (Pds) suggests a key role for pendrin in the inner ear. Proc Natl Acad Sci U S A 1999; 96:9727. http://www.uptodate.com/patients/content/topic.do?topicKey=pediendo/6330 open pop Eastern Mediterranean Health Journal Kabakkaya Y et al. Pendred’s syndrome. Annals of otology, rhinology, and laryngology, 1993, 102(4 Pt 1):285–8. 23. Deol MS. http://www.emro.who.int/Publications/EMHJ/0701/22.htm open pop Centre de Référence pour les Anomalies du Développement - Ile-de ... ... Catros H, Journel H, Drouin-Garraud V, Obstoy MF, Toutain A, Oden S, Toublanc JE, Couderc R, Petit C, Garabedian EN, Marlin S. Screening of SLC26A4 (PDS) gene in Pendred's syndrome ... http://cr-adif.org/publications_du_centre.html open pop Molecular mechanisms of epithelial cell-specific expression and ... Expression pattern of the mouse ortholog of the Pendred's syndrome gene (Pds) suggests a key role for pendrin in the inner ear. Proc Natl Acad Sci USA 96: 9727–9732, 1999. http://ajpcell.physiology.org/cgi/content/full/294/5/C1261 open pop SLC26A4 Gene - GeneCards | S26A4 Protein | S26A4 Antibody EntrezGene summary for SLC26A4: Mutations in this gene are associated with Pendred syndrome, the most common form of syndromic deafness, an autosomal-recessive disease. http://ophid.utoronto.ca/cgi-bin/carddisp.pl?gene=SLC26A4 open pop |
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