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LADD syndrome is caused by FGF10 mutationsMILUNSKY, J. M; ZHAO, G; MAHER, T. A et al.Clinical genetics. 2006, Vol 69, Num 4, pp 349-354, issn 0009-9163, 6 p.Article

FHGT2, GHG8, GHG10 and BMP7 as candidate genes for hypospadiasBELEZA -MEIRELES, Ana; LUNDBERG, Fredrik; LAGERSTEDT, Kristina et al.European journal of human genetics. 2007, Vol 15, Num 4, pp 405-410, issn 1018-4813, 6 p.Article

Evaluation of Genes Involved in Limb Development, Angiogenesis, and Coagulation as Risk Factors for Congenital Limb DeficienciesBROWNE, Marilyn L; CARTER, Tonia C; KAY, Denise M et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 10, pp 2463-2472, issn 1552-4825, 10 p.Article

Fgf10 is an oncogene activated by MMTV insertional mutagenesis in mouse mammary tumors and overexpressed in a subset of human breast carcinomasTHEODOROU, Vassiliki; BOER, Mandy; WEIGELT, Britta et al.Oncogene (Basingstoke). 2004, Vol 23, Num 36, pp 6047-6055, issn 0950-9232, 9 p.Article

Overexpression of Fibroblast Growth Factor-10 during Both Inflammatory and Fibrotic Phases Attenuates Bleomycin-induced Pulmonary Fibrosis in MiceGUPTE, Varsha V; RAMASAMY, Suresh K; BELLUSCI, Saverio et al.American journal of respiratory and critical care medicine. 2009, Vol 180, Num 5, pp 424-436, issn 1073-449X, 13 p.Article

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