176 related articles for article (PubMed ID: 8673103)
1. 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]
2. A paternal wash in Apert syndrome.
Sapienza C
Nat Genet; 1996 May; 13(1):9-10. PubMed ID: 8673111
[No Abstract] [Full Text] [Related]
3. [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]
4. Paternal origin of FGFR2 mutations in sporadic cases of Crouzon syndrome and Pfeiffer syndrome.
Glaser RL; Jiang W; Boyadjiev SA; Tran AK; Zachary AA; Van Maldergem L; Johnson D; Walsh S; Oldridge M; Wall SA; Wilkie AO; Jabs EW
Am J Hum Genet; 2000 Mar; 66(3):768-77. PubMed ID: 10712195
[TBL] [Abstract][Full Text] [Related]
5. Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome.
Wilkie AO; Slaney SF; Oldridge M; Poole MD; Ashworth GJ; Hockley AD; Hayward RD; David DJ; Pulleyn LJ; Rutland P
Nat Genet; 1995 Feb; 9(2):165-72. PubMed ID: 7719344
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. Development. There's something curious about paternal-age effects.
Crow JF
Science; 2003 Aug; 301(5633):606-7. PubMed ID: 12893932
[No Abstract] [Full Text] [Related]
9. 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]
10. 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]
11. Molecular diagnosis of Apert syndrome in Chinese patients.
Tsai FJ; Tsai CH; Peng CT; Lin SP; Hwu WL; Wang TR; Lee CC; Wu JY
Acta Paediatr Taiwan; 1999; 40(1):31-3. PubMed ID: 10910582
[TBL] [Abstract][Full Text] [Related]
12. [From gene to disease; craniosynostosis syndromes due to FGFR2-mutation].
van Ravenswaaij-Arts CM; van den Ouweland AM; Hoogeboom AJ; Herbergs J; Pals G
Ned Tijdschr Geneeskd; 2002 Jan; 146(2):63-6. PubMed ID: 11820058
[TBL] [Abstract][Full Text] [Related]
13. A further mutation of the FGFR2 tyrosine kinase domain in mild Crouzon syndrome.
de Ravel TJ; Taylor IB; Van Oostveldt AJ; Fryns JP; Wilkie AO
Eur J Hum Genet; 2005 Apr; 13(4):503-5. PubMed ID: 15523492
[TBL] [Abstract][Full Text] [Related]
14. Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes.
Rutland P; Pulleyn LJ; Reardon W; Baraitser M; Hayward R; Jones B; Malcolm S; Winter RM; Oldridge M; Slaney SF
Nat Genet; 1995 Feb; 9(2):173-6. PubMed ID: 7719345
[TBL] [Abstract][Full Text] [Related]
15. Mutation of the fibroblast growth factor receptor 2 gene in Japanese patients with Apert syndrome.
Matsumoto K; Urano Y; Kubo Y; Nakanishi H; Arase S
Plast Reconstr Surg; 1998 Feb; 101(2):307-11. PubMed ID: 9462761
[TBL] [Abstract][Full Text] [Related]
16. Gain-of-function amino acid substitutions drive positive selection of FGFR2 mutations in human spermatogonia.
Goriely A; McVean GA; van Pelt AM; O'Rourke AW; Wall SA; de Rooij DG; Wilkie AO
Proc Natl Acad Sci U S A; 2005 Apr; 102(17):6051-6. PubMed ID: 15840724
[TBL] [Abstract][Full Text] [Related]
17. De novo alu-element insertions in FGFR2 identify a distinct pathological basis for Apert syndrome.
Oldridge M; Zackai EH; McDonald-McGinn DM; Iseki S; Morriss-Kay GM; Twigg SR; Johnson D; Wall SA; Jiang W; Theda C; Jabs EW; Wilkie AO
Am J Hum Genet; 1999 Feb; 64(2):446-61. PubMed ID: 9973282
[TBL] [Abstract][Full Text] [Related]
18. FGFR2 mutations among Thai children with Crouzon and Apert syndromes.
Shotelersuk V; Mahatumarat C; Ittiwut C; Rojvachiranonda N; Srivuthana S; Wacharasindhu S; Tongkobpetch S
J Craniofac Surg; 2003 Jan; 14(1):101-4; discussion 105-7. PubMed ID: 12544231
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]