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8. Achondroplastic dog breeds have no mutations in the transmembrane domain of the FGFR-3 gene. Martínez S; Valdés J; Alonso RA Can J Vet Res; 2000 Oct; 64(4):243-5. PubMed ID: 11041504 [TBL] [Abstract][Full Text] [Related]
9. Atypical radiological findings in achondroplasia with uncommon mutation of the fibroblast growth factor receptor-3 (FGFR-3) gene (Gly to Cys transition at codon 375). Nishimura G; Fukushima Y; Ohashi H; Ikegawa S Am J Med Genet; 1995 Nov; 59(3):393-5. PubMed ID: 8599370 [No Abstract] [Full Text] [Related]
10. [Gly380Arg and Asn540Lys mutations of fibroblast growth factor receptor 3 in achondroplasia and hypochndroplasia in the Spanish population]. Ezquieta Zubicaray B; Iguacel AO; Varela Junquera JM; Jariego Fente CM; González Gancedo P; Gracia Bouthelier R Med Clin (Barc); 1999 Mar; 112(8):290-3. PubMed ID: 10207844 [TBL] [Abstract][Full Text] [Related]
11. [Updated treatment of achondroplasia]. Seino Y Clin Calcium; 2009 Mar; 19(3):432-6. PubMed ID: 19252254 [TBL] [Abstract][Full Text] [Related]
12. Genotyping of the G1138A mutation of the FGFR3 gene in patients with achondroplasia using high-resolution melting analysis. Hung CC; Lee CN; Chang CH; Jong YJ; Chen CP; Hsieh WS; Su YN; Lin WL Clin Biochem; 2008 Feb; 41(3):162-6. PubMed ID: 18199430 [TBL] [Abstract][Full Text] [Related]
13. Achondroplasia in diverse Jewish and Arab populations in Israel: clinical and molecular characterization. Falik-Zaccai TC; Shachak E; Abeliovitch D; Lerer I; Shefer R; Carmi R; Ries L; Friedman M; Shohat M; Borochowitz Z Isr Med Assoc J; 2000 Aug; 2(8):601-4. PubMed ID: 10979354 [TBL] [Abstract][Full Text] [Related]
14. Probable case of achondroplasia-hypochondroplasia compound. Kelly TE Birth Defects Orig Artic Ser; 1974; 10(12):360-1. PubMed ID: 4461068 [No Abstract] [Full Text] [Related]
15. Cartilage-hair hypoplasia. Fryns JP; Pedersen JC; Pardon W; Van den Berghe H Acta Paediatr Belg; 1980; 33(4):265-7. PubMed ID: 7282359 [No Abstract] [Full Text] [Related]
16. [Clinical picture, diagnosis and genetic aspects of hypochondroplasia]. Meerson EM; Iukina GP; Nechvolodova OL Ortop Travmatol Protez; 1976 Sep; (9):40-4. PubMed ID: 1012689 [No Abstract] [Full Text] [Related]
17. Achondroplasia in two sisters with normal parents. Bowen P Birth Defects Orig Artic Ser; 1974; 10(12):31-6. PubMed ID: 4461062 [No Abstract] [Full Text] [Related]
18. The molecular basis of hereditary skeletal disorders. Hästbacka J Ann Med; 1995 Aug; 27(4):433-4. PubMed ID: 8519503 [No Abstract] [Full Text] [Related]
19. [Blood zinc levels in an achondroplastic child and her relatives]. Ponticiello L; D'Ambrosio E; Ponticelli L Pediatria (Napoli); 1983; 91(2-3):315-9. PubMed ID: 6664739 [No Abstract] [Full Text] [Related]
20. [Genetic study of achondroplasia]. Bouvet JP; Maroteaux P; Feingold J Ann Genet; 1971 Jun; 14(2):127-31. PubMed ID: 5314799 [No Abstract] [Full Text] [Related] [Next] [New Search]