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Disruption of ALX1 causes extreme microphthalmia and severe facial clefting: expanding the spectrum of autosomal-recessive ALX-related frontonasal dysplasia E Uz, Y Alanay, D Aktas, I Vargel, S Gucer, G Tuncbilek, F von Eggeling, ... The American Journal of Human Genetics 86 (5), 789-796, 2010 | 160 | 2010 |
Homozygous mutations in fibroblast growth factor 3 are associated with a new form of syndromic deafness characterized by inner ear agenesis, microtia, and microdontia M Tekin, BÖ Hişmi, S Fitoz, H Özdağ, FB Cengiz, A Sırmacı, I Aslan, ... The American Journal of Human Genetics 80 (2), 338-344, 2007 | 143 | 2007 |
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Mutation analysis of CBP and PCAF reveals rare inactivating mutations in cancer cell lines but not in primary tumours H Özdağ, SJ Batley, A Försti, NG Iyer, Y Daigo, J Boutell, MJ Arends, ... British journal of cancer 87 (10), 1162-1165, 2002 | 78 | 2002 |
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A truncating mutation in SERPINB6 is associated with autosomal-recessive nonsyndromic sensorineural hearing loss A Sırmacı, S Erbek, J Price, M Huang, D Duman, FB Cengiz, G Bademci, ... The American Journal of Human Genetics 86 (5), 797-804, 2010 | 69 | 2010 |
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SLCO1B1 polymorphisms are associated with drug intolerance in childhood leukemia maintenance therapy I Eldem, D Yavuz, Ö Cumaogullari, T Ileri, EÜ Ince, M Ertem, BD Erdogan, ... Journal of Pediatric Hematology/Oncology 40 (5), e289-e294, 2018 | 20 | 2018 |