These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
118 related articles for article (PubMed ID: 8723559)
21. A case of oculo-facio-cardio-dental syndrome with integrated orthodontic-prosthodontic treatment. Kawamoto T; Motohashi N; Ohyama K Cleft Palate Craniofac J; 2004 Jan; 41(1):84-94. PubMed ID: 14697064 [TBL] [Abstract][Full Text] [Related]
22. Otodental syndrome, oculo-facio-cardio-dental (OFCD) syndrome, and lobodontia: dental disorders of interest to the pediatric radiologist. Gorlin RJ Pediatr Radiol; 1998 Oct; 28(10):802-4. PubMed ID: 9799305 [TBL] [Abstract][Full Text] [Related]
23. Six additional cases of the KBG syndrome: clinical reports and outline of the diagnostic criteria. Zollino M; Battaglia A; D'Avanzo MG; Della Bruna MM; Marini R; Scarano G; Cappa M; Neri G Am J Med Genet; 1994 Sep; 52(3):302-7. PubMed ID: 7810561 [TBL] [Abstract][Full Text] [Related]
24. Familial syndrome of unusual triangular facies associated with cleft palate, malocclusion, midfacial hypoplasia and sensorineural hearing loss in two siblings. Is it a new autosomal recessive syndrome? Balcı S; Akcan B; Vargel İ; Tümer C; Enacar A Clin Dysmorphol; 2004 Apr; 13(2):71-74. PubMed ID: 15057120 [TBL] [Abstract][Full Text] [Related]
25. Does the cranio-cerebello-cardiac syndrome (3C syndrome) include abdominal malformations? Mégarbané A; Haddad J Clin Dysmorphol; 1999 Oct; 8(4):305-7. PubMed ID: 10532184 [TBL] [Abstract][Full Text] [Related]
26. Ohdo-like blepharophimosis syndrome with distinctive facies, neonatal hypotonia, mental retardation and hypoplastic teeth. Clayton-Smith J; Krajewska-Walasek M; Fryer A; Donnai D Clin Dysmorphol; 1994 Apr; 3(2):115-20. PubMed ID: 8055130 [TBL] [Abstract][Full Text] [Related]
27. A previously undescribed autosomal recessive multiple congenital anomalies/mental retardation (MCA/MR) syndrome with fronto-nasal dysostosis, cleft lip/palate, limb hypoplasia, and postaxial poly-syndactyly: acro-fronto-facio-nasal dysostosis syndrome. Richieri-Costa A; Colletto GM; Gollop TR; Masiero D Am J Med Genet; 1985 Apr; 20(4):631-8. PubMed ID: 2986457 [TBL] [Abstract][Full Text] [Related]
28. Further contributions to the study of the syndrome of Hallermann and Streiff. (Congenital cataract with "bird's face"). PONTE F Ophthalmologica; 1962; 143():399-408. PubMed ID: 14487806 [No Abstract] [Full Text] [Related]
29. Rubinstein-Taybi syndrome: objective evaluation of craniofacial structure. Allanson JE; Hennekam RC Am J Med Genet; 1997 Sep; 71(4):414-9. PubMed ID: 9286447 [TBL] [Abstract][Full Text] [Related]
30. A new syndrome with cardiac malformation, cleft lip-palate, microcephaly and digital anomalies? Perçin EF; Düzcan F; Kafali G; Sezgin I Clin Genet; 1995 Nov; 48(5):264-7. PubMed ID: 8825606 [TBL] [Abstract][Full Text] [Related]
32. O--short stature with abnormalities of the cranium and limbs. Jorgenson RJ Birth Defects Orig Artic Ser; 1974; 10(5):249-51. PubMed ID: 4469995 [No Abstract] [Full Text] [Related]
33. Variability of the cranial and dental phenotype in Williams syndrome. Axelsson S Swed Dent J Suppl; 2005; (170):3-67. PubMed ID: 15762376 [TBL] [Abstract][Full Text] [Related]
35. Oculofaciocardiodental and Lenz microphthalmia syndromes result from distinct classes of mutations in BCOR. Ng D; Thakker N; Corcoran CM; Donnai D; Perveen R; Schneider A; Hadley DW; Tifft C; Zhang L; Wilkie AO; van der Smagt JJ; Gorlin RJ; Burgess SM; Bardwell VJ; Black GC; Biesecker LG Nat Genet; 2004 Apr; 36(4):411-6. PubMed ID: 15004558 [TBL] [Abstract][Full Text] [Related]
36. Mental retardation, congenital heart defect, cleft palate, short stature, and facial anomalies: a new X-linked multiple congenital anomalies/mental retardation syndrome: clinical description and molecular studies. Hamel BC; Mariman EC; van Beersum SE; Schoonbrood-Lenssen AM; Ropers HH Am J Med Genet; 1994 Jul; 51(4):591-7. PubMed ID: 7943045 [TBL] [Abstract][Full Text] [Related]
37. Radiculomegaly of canines in oculofaciocardiodental syndrome. Oh SH; Kang JH; Kang JH; Seo YK; Lee SR; Choi YS; Hwang EH Oral Radiol; 2019 Sep; 35(3):326-330. PubMed ID: 30484210 [TBL] [Abstract][Full Text] [Related]
38. Oto-palato-digital syndrome type II. Stoll C; Alembik Y Genet Couns; 1994; 5(1):61-6. PubMed ID: 8031537 [TBL] [Abstract][Full Text] [Related]
39. The Greig cephalopolysyndactyly syndrome: report of a family and review of the literature. Gollop TR; Fontes LR Am J Med Genet; 1985 Sep; 22(1):59-68. PubMed ID: 3901752 [TBL] [Abstract][Full Text] [Related]
40. New mental retardation syndrome with hearing impairment, distinct facial appearance, and skeletal anomalies. Finucane B; Kurtz MB; Scott CI Am J Med Genet; 1992 Jul; 43(5):844-7. PubMed ID: 1642273 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]