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.
134 related articles for article (PubMed ID: 3174485)
1. [Cohen syndrome. Contribution to its clinical delineation]. Lapetina F; Piantoni G; Canino R; Teza F; Ferrarini D Pediatr Med Chir; 1988; 10(2):217-21. PubMed ID: 3174485 [TBL] [Abstract][Full Text] [Related]
2. Opitz trigonocephaly syndrome and terminal transverse limb reduction defects. Fryns JP; Snoeck L; Kleczkowska A; Van den Berghe H Helv Paediatr Acta; 1985; 40(6):485-8. PubMed ID: 3830973 [TBL] [Abstract][Full Text] [Related]
3. Mental retardation, hypotonia, obesity, ocular, facial, dental, and limb abnormalities (Cohen syndrome). Report of three patients. Goecke T; Majewski F; Kauther KD; Sterzel U Eur J Pediatr; 1982 Jul; 138(4):338-40. PubMed ID: 7128643 [TBL] [Abstract][Full Text] [Related]
4. A particular form of cranio-facio-mandibular dysostosis with type B brachydactylia. Van Damme W; Touitou D J Belge Radiol; 1980; 63(4):491-6. PubMed ID: 7204325 [No Abstract] [Full Text] [Related]
5. Cleidocranial dysostosis, severe micrognathism, bilateral absence of thumbs and first metatarsal bone, and distal aphalangia: a new genetic syndrome. Yunis E; VarĂ³n H Am J Dis Child; 1980 Jul; 134(7):649-53. PubMed ID: 7395825 [TBL] [Abstract][Full Text] [Related]
6. Congenital micrognathia and partial adactylia. Test D; Cerami J; Schow CE J Oral Surg; 1976 Jun; 34(6):559-65. PubMed ID: 1063848 [TBL] [Abstract][Full Text] [Related]
7. Cohen syndrome: further delineation and inheritance. Kousseff BG Am J Med Genet; 1981; 9(1):25-30. PubMed ID: 7246618 [TBL] [Abstract][Full Text] [Related]
8. Cone-shaped epiphyses in the distal phalanges. Case report of a child with anorchia. Saldino RM; Marshall S; Taybi H Radiol Clin Biol; 1972; 41(6):449-52. PubMed ID: 4404981 [No Abstract] [Full Text] [Related]
9. [Cohen syndrome. A new case and review of the literature]. Calzolari S; Ballardini M; De Marco P Minerva Pediatr; 1995 Mar; 47(3):83-7. PubMed ID: 7791717 [TBL] [Abstract][Full Text] [Related]
13. [Ullrich-Feichtiger syndrome in a 3-year-old boy]. Mazur B; Buszman Z Pol Tyg Lek; 1992 Mar 2-9; 47(9-10):234-5. PubMed ID: 1437827 [TBL] [Abstract][Full Text] [Related]
14. Acrania: a manifestation of the Adams-Oliver syndrome. Chitayat D; Meunier C; Hodgkinson KA; Robb L; Azouz M Am J Med Genet; 1992 Nov; 44(5):562-6. PubMed ID: 1481809 [TBL] [Abstract][Full Text] [Related]
15. The Cohen syndrome: report of a case. Naritomi K; Chinen Y Jpn J Hum Genet; 1997 Sep; 42(3):457-9. PubMed ID: 12503195 [TBL] [Abstract][Full Text] [Related]
16. Trichorhinophalangeal dysplasia (Giedion syndrome). A case report. Kuna GB; Collipp PJ; Balsam D Clin Pediatr (Phila); 1978 Jan; 17(1):96-8. PubMed ID: 618703 [TBL] [Abstract][Full Text] [Related]
17. A new form of spondyloperipheral dysplasia with facial dysmorphism, flattened vertebrae, hypoplastic pelvis, brachydactyly and soft tissue syndactyly. Kitoh H; Lachman RS Pediatr Radiol; 2001 Jan; 31(1):23-6. PubMed ID: 11200993 [TBL] [Abstract][Full Text] [Related]
18. Oculodentodigital dysplasia. A case report. Itro A; Marra A; Urciuolo V; Difalco P; Amodio A Minerva Stomatol; 2005; 54(7-8):453-9. PubMed ID: 16211004 [TBL] [Abstract][Full Text] [Related]