Human Genome Epidemiology Literature Finder
Records 1 - 6 (of 6 Records) |
Query Trace: Syndrome and FOXI1[original query] |
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Phenotypic analyses and mutation screening of the SLC26A4 and FOXI1 genes in 101 Taiwanese families with bilateral nonsyndromic enlarged vestibular aqueduct (DFNB4) or Pendred syndrome. Audiology & neuro-otology 2010 15 (1): 57-66. Wu Chen-Chi, Lu Ying-Chang, Chen Pei-Jer, Yeh Po-Lin, Su Yi-Nin, Hwu Wuh-Liang, Hsu Chuan-J |
Screening of SLC26A4, FOXI1 and KCNJ10 genes in unilateral hearing impairment with ipsilateral enlarged vestibular aqueduct. International journal of pediatric otorhinolaryngology 2010 Sep 74 (9): 1049-53. Jonard Laurence, Niasme-Grare Magali, Bonnet Crystel, Feldmann Delphine, Rouillon Isabelle, Loundon Natalie, Calais Catherine, Catros Hélène, David Albert, Dollfus Hélène, Drouin-Garraud Valérie, Duriez Françoise, Eliot Marie Madeleine, Fellmann Florence, Francannet Christine, Gilbert-Dussardier Brigitte, Gohler Catherine, Goizet Cyril, Journel Hubert, Mom Thierry, Thuillier-Obstoy Marie-Françoise, Couderc Remy, Garabédian Eréa Noël, Denoyelle Françoise, Marlin Sandri |
Identification of SLC26A4 mutations in patients with hearing loss and enlarged vestibular aqueduct using high-resolution melting curve analysis. Genetic testing and molecular biomarkers 2011 May 15 (5): 365-8. Mercer Stephen, Mutton Patricia, Dahl Hans-Henrik |
Heredity and cardiometabolic risk: naturally occurring polymorphisms in the human neuropeptide Y(2) receptor promoter disrupt multiple transcriptional response motifs. Journal of hypertension 2012 Nov . Wei Z, Zhang K, Wen G, Balasubramanian K, Shih PA, Rao F, Friese RS, Miramontes-Gonzalez JP, Schmid-Schoenbein GW, Kim HS, Mahata SK, O'Connor DT |
Lack of significant association between mutations of KCNJ10 or FOXI1 and SLC26A4 mutations in Pendred syndrome/enlarged vestibular aqueducts. BMC medical genetics 2013 14 85. Landa Priya, Differ Ann-Marie, Rajput Kaukab, Jenkins Lucy, Bitner-Glindzicz Mar |
Targeted Next-Generation Sequencing Facilitates Genetic Diagnosis and Provides Novel Pathogenetic Insights into Deafness with Enlarged Vestibular Aqueduct. The Journal of molecular diagnostics : JMD 2018 10 21 (1): 138-148. Lin Yin-Hung, Wu Chen-Chi, Lin Yi-Hsin, Lu Ying-Chang, Chen Chih-Shan, Liu Tien-Chen, Chen Pei-Lung, Hsu Chuan-J |
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