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44. Oculo-dento-digital dysplasia (OMIM *164200). Full manifestation of the syndrome in a 9.5 year-old girl and type III syndactyly in the father. Ioan DM; Dagomiz D; Fryns JP Genet Couns; 2002; 13(2):187-9. PubMed ID: 12150221 [TBL] [Abstract][Full Text] [Related]
45. Dental findings in Kabuki make-up syndrome: a case report. Rocha CT; Peixoto IT; Fernandes PM; Torres CP; de Queiroz AM Spec Care Dentist; 2008; 28(2):53-7. PubMed ID: 18402617 [TBL] [Abstract][Full Text] [Related]
47. Short rib-polydactyly syndrome, type 3 with chondrocytic inclusions: report of a case and review of the literature. Yang SS; Lin CS; Al Saadi A; Nangia BS; Bernstein J Am J Med Genet; 1980; 7(2):205-13. PubMed ID: 7468648 [TBL] [Abstract][Full Text] [Related]
48. Orofacial manifestations in the Cri du Chat syndrome (5p-). Scully C; Davison MF J Dent; 1979 Dec; 7(4):313-20. PubMed ID: 292652 [No Abstract] [Full Text] [Related]
49. [Ellis-van Creveld syndrome or chondroectodermal dysplasia. (Description of a clinical case)]. Miotti A; Miotti F G Stomatol Ortognatodonzia; 1983; 2(1):87-9. PubMed ID: 6583190 [No Abstract] [Full Text] [Related]
50. [Pediatric dentistry syndrome with various oro-systemic congenital abnormalities (condroectodermal dysplasia or oro-digital-facial disorders); presentation of a case]. Menendez OR; Perez ER Cent Estud Recur Odontol Nino; 1981 Apr; 6(1):45-50. PubMed ID: 6942943 [No Abstract] [Full Text] [Related]
51. Unknown syndrome: Noonan-like craniofacial features, digital anomalies, and premature birth. Shepherd RC; Goudie DR; Tolmie JL J Med Genet; 1989 Jul; 26(7):470-2. PubMed ID: 2746622 [TBL] [Abstract][Full Text] [Related]
52. The atrioventricular canal defect is the congenital heart disease connecting short rib-polydactyly and oral-facial-digital syndromes. Digilio MC; Marino B; Giannotti A; Dallapiccola B Am J Med Genet; 1997 Jan; 68(1):110-2. PubMed ID: 8986290 [No Abstract] [Full Text] [Related]
53. Angel shaped phalangeal dysplasia, hip dysplasia, and positional teeth abnormalities are part of the brachydactyly C spectrum associated with CDMP-1 mutations. Holder-Espinasse M; Escande F; Mayrargue E; Dieux-Coeslier A; Fron D; Doual-Bisser A; Boute-Benejean O; Robert Y; Porchet N; Manouvrier-Hanu S J Med Genet; 2004 Jun; 41(6):e78. PubMed ID: 15173244 [No Abstract] [Full Text] [Related]
54. Oral manifestations of Ellis-van Creveld syndrome: report of two siblings with unusual dental anomalies. Hattab FN; Yassin OM; Sasa IS J Clin Pediatr Dent; 1998; 22(2):159-65. PubMed ID: 9643193 [TBL] [Abstract][Full Text] [Related]
55. Recurrence of short rib polydactyly syndrome - a rare skeletal dysplasia. Malhotra N; Sood M Eur J Obstet Gynecol Reprod Biol; 2000 Apr; 89(2):193-5. PubMed ID: 10725582 [TBL] [Abstract][Full Text] [Related]
57. Oral findings in a group of newborn Swedish children. Flinck A; Paludan A; Matsson L; Holm AK; Axelsson I Int J Paediatr Dent; 1994 Jun; 4(2):67-73. PubMed ID: 7748853 [TBL] [Abstract][Full Text] [Related]
58. A Rare Case of Hanhart Syndrome with Mild Developmental Delay. Gulec Ceylan G; Tos T; Sari E Genet Couns; 2016; 27(2):219-22. PubMed ID: 29485825 [TBL] [Abstract][Full Text] [Related]
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60. Polydactyly, conical teeth, nail dysplasia, and short limbs: a new autosomal dominant malformation syndrome. Curry CJ; Hall BD Birth Defects Orig Artic Ser; 1979; 15(5B):253-63. PubMed ID: 526581 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]