112 related articles for article (PubMed ID: 9211121)
1. The feet in Crouzon syndrome.
Anderson PJ; Hall CM; Evans RD; Jones BM; Hayward RD
J Craniofac Genet Dev Biol; 1997; 17(1):43-7. PubMed ID: 9211121
[TBL] [Abstract][Full Text] [Related]
2. The feet in Pfeiffer's syndrome.
Anderson PJ; Hall CM; Evans RD; Jones BM; Hayward RD
J Craniofac Surg; 1998 Jan; 9(1):83-7. PubMed ID: 9558574
[TBL] [Abstract][Full Text] [Related]
3. Jackson-Weiss syndrome registered in four successive generations. The facies of Crouzon's syndrome with foot abnormalities.
Stanković B; Krstić V; Stankov B; Jojić L; Nagulić M; Artiko G
Doc Ophthalmol; 1994; 85(3):281-6. PubMed ID: 7924855
[TBL] [Abstract][Full Text] [Related]
4. Fibroblast growth factor receptor 3 (FGFR3) transmembrane mutation in Crouzon syndrome with acanthosis nigricans.
Meyers GA; Orlow SJ; Munro IR; Przylepa KA; Jabs EW
Nat Genet; 1995 Dec; 11(4):462-4. PubMed ID: 7493034
[TBL] [Abstract][Full Text] [Related]
5. Clinicogenetic study of Turkish patients with syndromic craniosynostosis and literature review.
Nur BG; Pehlivanoğlu S; Mıhçı E; Calışkan M; Demir D; Alper OM; Kayserili H; Lüleci G
Pediatr Neurol; 2014 May; 50(5):482-90. PubMed ID: 24656465
[TBL] [Abstract][Full Text] [Related]
6. Palatal anomalies in the syndromes of Apert and Crouzon.
Peterson SJ; Pruzansky S
Cleft Palate J; 1974 Oct; 11():394-403. PubMed ID: 4530751
[No Abstract] [Full Text] [Related]
7. Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2.
Jabs EW; Li X; Scott AF; Meyers G; Chen W; Eccles M; Mao JI; Charnas LR; Jackson CE; Jaye M
Nat Genet; 1994 Nov; 8(3):275-9. PubMed ID: 7874170
[TBL] [Abstract][Full Text] [Related]
8. Hand anomalies in Crouzon syndrome.
Anderson PJ; Hall CM; Evans RD; Jones BM; Hayward RD
Skeletal Radiol; 1997 Feb; 26(2):113-5. PubMed ID: 9060103
[TBL] [Abstract][Full Text] [Related]
9. Comparative study of normal, Crouzon, and Apert craniofacial morphology using finite element scaling analysis.
Richtsmeier JT
Am J Phys Anthropol; 1987 Dec; 74(4):473-93. PubMed ID: 3442299
[TBL] [Abstract][Full Text] [Related]
10. The pattern of skeletal anomalies in the cervical spine, hands and feet in patients with Saethre-Chotzen syndrome and Muenke-type mutation.
Trusen A; Beissert M; Collmann H; Darge K
Pediatr Radiol; 2003 Mar; 33(3):168-72. PubMed ID: 12612814
[TBL] [Abstract][Full Text] [Related]
11. Morphology and growth of the mandible in Crouzon, Apert, and Pfeiffer syndromes.
Boutros S; Shetye PR; Ghali S; Carter CR; McCarthy JG; Grayson BH
J Craniofac Surg; 2007 Jan; 18(1):146-50. PubMed ID: 17251854
[TBL] [Abstract][Full Text] [Related]
12. Cervical spine anomalies in the craniosynostosis syndromes.
Hemmer KM; McAlister WH; Marsh JL
Cleft Palate J; 1987 Oct; 24(4):328-33. PubMed ID: 3479279
[TBL] [Abstract][Full Text] [Related]
13. The feet in Apert's syndrome.
Anderson PJ; Hall CM; Evans RD; Hayward RD; Jones BM
J Pediatr Orthop; 1999; 19(4):504-7. PubMed ID: 10413001
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Dental maturation in children with the syndrome of crouzon and apert.
Reitsma JH; Balk-Leurs IH; Ongkosuwito EM; Wattel E; Prahl-Andersen B
Cleft Palate Craniofac J; 2014 Nov; 51(6):639-44. PubMed ID: 24021057
[TBL] [Abstract][Full Text] [Related]
16. Two craniosynostotic syndrome loci, Crouzon and Jackson-Weiss, map to chromosome 10q23-q26.
Li X; Lewanda AF; Eluma F; Jerald H; Choi H; Alozie I; Proukakis C; Talbot CC; Vander Kolk C; Bird LM
Genomics; 1994 Jul; 22(2):418-24. PubMed ID: 7806229
[TBL] [Abstract][Full Text] [Related]
17. Comparing patients with Apert and Crouzon syndromes--clinical features and cranio-maxillofacial surgical reconstruction.
Stavropoulos D; Tarnow P; Mohlin B; Kahnberg KE; Hagberg C
Swed Dent J; 2012; 36(1):25-34. PubMed ID: 22611902
[TBL] [Abstract][Full Text] [Related]
18. Nasopharyngeal dysmorphology in the syndromes of Apert and Crouzon.
Peterson-Falzone SJ; Pruzansky S; Parris PJ; Laffer JL
Cleft Palate J; 1981 Oct; 18(4):237-50. PubMed ID: 6945155
[TBL] [Abstract][Full Text] [Related]
19. Dentofacial features of a family with Crouzon syndrome. Case reports.
Singer SL; Walpole I; Brogan WF; Goldblatt J
Aust Dent J; 1997 Feb; 42(1):11-7. PubMed ID: 9078640
[TBL] [Abstract][Full Text] [Related]
20. Hydrocephalus and mental retardation in craniosynostosis.
Noetzel MJ; Marsh JL; Palkes H; Gado M
J Pediatr; 1985 Dec; 107(6):885-92. PubMed ID: 4067746
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
