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22. The spectrum of frontonasal dysplasia in an inbred pedigree. Moreno Fuenmayor H Clin Genet; 1980 Feb; 17(2):137-42. PubMed ID: 7363499 [TBL] [Abstract][Full Text] [Related]
23. Germinal mosaicism in Crouzon syndrome. A family with three affected siblings of normal parents. Navarrete C; Peña R; Peñaloza R; Salamanca F Clin Genet; 1991 Jul; 40(1):29-34. PubMed ID: 1884515 [TBL] [Abstract][Full Text] [Related]
24. Are the acrocephalosyndactyly syndromes variable expressions of a single gene defect? Escobar V; Bixler D Birth Defects Orig Artic Ser; 1977; 13(3C):139-54. PubMed ID: 890108 [TBL] [Abstract][Full Text] [Related]
25. Lumpers, splitters, and FGFRs. Winter RM; Reardon W Am J Med Genet; 1996 Jun; 63(3):501-2. PubMed ID: 8737660 [No Abstract] [Full Text] [Related]
26. On the classification of the acrocephalosyndactyly syndromes. Escobar V; Bixler D Clin Genet; 1977 Sep; 12(3):169-78. PubMed ID: 908170 [TBL] [Abstract][Full Text] [Related]
27. Studies of malformation syndromes of man XXXIX: a craniosynostosis-craniofacial dysostosis syndrome with mental retardation and other malformations: "craniofacial dyssynostosis". Neuhäuser G; Kaveggia EG; Opitz JM Eur J Pediatr; 1976 Aug; 123(1):15-28. PubMed ID: 954768 [TBL] [Abstract][Full Text] [Related]
28. Crouzon syndrome is not linked to craniosynostosis loci at 7p and 5qter. Reardon W; van Herwerden L; Rose C; Jones B; Malcolm S; Winter RM J Med Genet; 1994 Mar; 31(3):219-21. PubMed ID: 8014970 [TBL] [Abstract][Full Text] [Related]
30. Iris dysplasia, orbital hypertelorism, and psychomotor retardation: a dominantly inherited developmental syndrome. De Hauwere RC; Leroy JG; Adriaenssens K; Van Heule R J Pediatr; 1973 Apr; 82(4):679-81. PubMed ID: 4633364 [No Abstract] [Full Text] [Related]
31. Familial craniosynostosis with oral anomalies. Kernohan DC; Nevin NC; Dodge JA Dev Med Child Neurol; 1970 Jun; 12(3):315-20. PubMed ID: 5433149 [No Abstract] [Full Text] [Related]
32. 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]
33. Expression analysis of an FGFR2 IIIc 5' splice site mutation (1084+3A->G). Kan R; Twigg SR; Berg J; Wang L; Jin F; Wilkie AO J Med Genet; 2004 Aug; 41(8):e108. PubMed ID: 15286168 [No Abstract] [Full Text] [Related]
34. A novel phenotypic pattern in X-linked inheritance: craniofrontonasal syndrome maps to Xp22. Feldman GJ; Ward DE; Lajeunie-Renier E; Saavedra D; Robin NH; Proud V; Robb LJ; Der Kaloustian V; Carey JC; Cohen MM; Cormier V; Munnich A; Zackai EH; Wilkie AO; Price RA; Muenke M Hum Mol Genet; 1997 Oct; 6(11):1937-41. PubMed ID: 9302274 [TBL] [Abstract][Full Text] [Related]
35. Frontonasal dysplasia: a family presenting autosomal dominant inheritance pattern. Koçak H; Ceylaner G Genet Couns; 2009; 20(1):63-8. PubMed ID: 19400543 [TBL] [Abstract][Full Text] [Related]
36. Craniosynostoses: phenotypic/molecular correlations. Cohen MM Am J Med Genet; 1995 Apr; 56(3):334-9. PubMed ID: 7778605 [No Abstract] [Full Text] [Related]