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2. Evidence for selective advantage of pathogenic FGFR2 mutations in the male germ line. Goriely A; McVean GA; Röjmyr M; Ingemarsson B; Wilkie AO Science; 2003 Aug; 301(5633):643-6. PubMed ID: 12893942 [TBL] [Abstract][Full Text] [Related]
3. Exclusive paternal origin of new mutations in Apert syndrome. Moloney DM; Slaney SF; Oldridge M; Wall SA; Sahlin P; Stenman G; Wilkie AO Nat Genet; 1996 May; 13(1):48-53. PubMed ID: 8673103 [TBL] [Abstract][Full Text] [Related]
4. A paternal wash in Apert syndrome. Sapienza C Nat Genet; 1996 May; 13(1):9-10. PubMed ID: 8673111 [No Abstract] [Full Text] [Related]
5. Description of a new mutation and characterization of FGFR1, FGFR2, and FGFR3 mutations among Brazilian patients with syndromic craniosynostoses. Passos-Bueno MR; Sertié AL; Richieri-Costa A; Alonso LG; Zatz M; Alonso N; Brunoni D; Ribeiro SF Am J Med Genet; 1998 Jul; 78(3):237-41. PubMed ID: 9677057 [TBL] [Abstract][Full Text] [Related]
6. [Nucleotide sequences at intron 6 and exon 7 junction of fibroblast growth factor receptor 2 and rapid mutational analysis in Apert syndrome]. Wada C; Ishigaki M; Toyo-oka Y; Yamabe H; Ohnuki Y; Takada F; Yamazaki Y; Ohtani H Rinsho Byori; 1996 May; 44(5):435-8. PubMed ID: 8676562 [TBL] [Abstract][Full Text] [Related]
7. Identical mutations in three different fibroblast growth factor receptor genes in autosomal dominant craniosynostosis syndromes. Bellus GA; Gaudenz K; Zackai EH; Clarke LA; Szabo J; Francomano CA; Muenke M Nat Genet; 1996 Oct; 14(2):174-6. PubMed ID: 8841188 [TBL] [Abstract][Full Text] [Related]
8. Vertebral anomalies and cartilaginous tracheal sleeve in three patients with Pfeiffer syndrome carrying the S351C FGFR2 mutation. Gonzales M; Heuertz S; Martinovic J; Delahaye S; Bazin A; Loget P; Pasquier L; Le Merrer M; Bonaventure J Clin Genet; 2005 Aug; 68(2):179-81. PubMed ID: 15996217 [No Abstract] [Full Text] [Related]
9. The Ser252Trp fibroblast growth factor receptor-2 (FGFR-2) mutation induces PKC-independent downregulation of FGFR-2 associated with premature calvaria osteoblast differentiation. Lemonnier J; Delannoy P; Hott M; Lomri A; Modrowski D; Marie PJ Exp Cell Res; 2000 Apr; 256(1):158-67. PubMed ID: 10739663 [TBL] [Abstract][Full Text] [Related]
10. Pfeiffer syndrome caused by haploinsufficient mutation of FGFR2. Tsukuno M; Suzuki H; Eto Y J Craniofac Genet Dev Biol; 1999; 19(4):183-8. PubMed ID: 10731087 [TBL] [Abstract][Full Text] [Related]
12. Two common mutations 934C to G and 937C to G of fibroblast growth factor receptor 2 (FGFR2) gene in Chinese patients with Apert syndrome. Tsai FJ; Hwu WL; Lin SP; Chang JG; Wang TR; Tsai CH Hum Mutat; 1998; Suppl 1():S18-9. PubMed ID: 9452027 [No Abstract] [Full Text] [Related]
13. A case of Pfeiffer syndrome type 1 with an A344P mutation in the FGFR2 gene. Shotelersuk V; Srivuthana S; Ittiwut C; Theamboonlers A; Mahatumarat C; Poovorawan Y Southeast Asian J Trop Med Public Health; 2001 Jun; 32(2):425-8. PubMed ID: 11556600 [TBL] [Abstract][Full Text] [Related]
14. Understanding the molecular basis of Apert syndrome. Ibrahimi OA; Chiu ES; McCarthy JG; Mohammadi M Plast Reconstr Surg; 2005 Jan; 115(1):264-70. PubMed ID: 15622262 [TBL] [Abstract][Full Text] [Related]