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.
88 related articles for article (PubMed ID: 8172246)
1. Properties of associations: identity, nature, and clinical criteria, with a commentary on why CHARGE and Goldenhar are not associations. Lubinsky MS Am J Med Genet; 1994 Jan; 49(1):21-5. PubMed ID: 8172246 [No Abstract] [Full Text] [Related]
2. Associations and syndromes: terminology in clinical genetics and birth defects epidemiology: comments on Khoury, Moore, and Evans. Opitz JM Am J Med Genet; 1994 Jan; 49(1):14-20. PubMed ID: 8172245 [No Abstract] [Full Text] [Related]
3. On the use of the term "syndrome" in clinical genetics and birth defects epidemiology. Khoury MJ; Moore CA; Evans JA Am J Med Genet; 1994 Jan; 49(1):26-8. PubMed ID: 8172247 [No Abstract] [Full Text] [Related]
5. Laryngomalacia, choanal atresia and renal anomaly in a newborn with Freeman-Sheldon syndrome phenotype. Tastekin A; Ikbal M; Ors R Genet Couns; 2004; 15(3):383-6. PubMed ID: 15517834 [No Abstract] [Full Text] [Related]
6. New case of axial mesodermal dysplasia sequence: epidemiologic evidence of a single entity. Martínez-Frías ML; Gomar JL Am J Med Genet; 1994 Jan; 49(1):74-6. PubMed ID: 8172254 [TBL] [Abstract][Full Text] [Related]
7. Lateral facial dysplasia (first and second branchial arch syndrome, hemifacial microsomia). Ross RB Birth Defects Orig Artic Ser; 1975; 11(7):51-9. PubMed ID: 1212511 [No Abstract] [Full Text] [Related]
8. The CHARGE association in a newborn infant. Akisü M; Ozkinay F; Ozyürek R; Küçüktaş A; Kültürsay N Turk J Pediatr; 1998; 40(2):283-7. PubMed ID: 9714686 [TBL] [Abstract][Full Text] [Related]
9. Developmental field defects and associations: epidemiological evidence of their relationship. Martínez-Frías ML Am J Med Genet; 1994 Jan; 49(1):45-51. PubMed ID: 8172250 [TBL] [Abstract][Full Text] [Related]
10. Oculo-auriculo-vertebral spectrum and the CHARGE association: clinical evidence for a common pathogenetic mechanism. Van Meter TD; Weaver DD Clin Dysmorphol; 1996 Jul; 5(3):187-96. PubMed ID: 8818446 [TBL] [Abstract][Full Text] [Related]
12. An approach to malformation syndromes. Hall JG Prog Clin Biol Res; 1985; 177():275-91. PubMed ID: 4011605 [No Abstract] [Full Text] [Related]
13. Oral-facial-skeletal syndromes. Neri G; Gurrieri F; Genuardi M Am J Med Genet; 1995 Nov; 59(3):365-8. PubMed ID: 8599363 [No Abstract] [Full Text] [Related]
14. Two brothers with Burn-McKeown syndrome. Wieczorek D; Teber OA; Lohmann D; Gillessen-Kaesbach G Clin Dysmorphol; 2003 Jul; 12(3):171-4. PubMed ID: 14564154 [TBL] [Abstract][Full Text] [Related]
15. CHARGE Association in newborns: a registry-based study. Källén K; Robert E; Mastroiacovo P; Castilla EE; Källén B Teratology; 1999 Dec; 60(6):334-43. PubMed ID: 10590394 [TBL] [Abstract][Full Text] [Related]
16. Costello syndrome: further clinical delineation, natural history, genetic definition, and nosology. Zampino G; Mastroiacovo P; Ricci R; Zollino M; Segni G; Martini-Neri ME; Neri G Am J Med Genet; 1993 Aug; 47(2):176-83. PubMed ID: 8213903 [TBL] [Abstract][Full Text] [Related]
17. [The sequence of fetal akinesia/hypokinesia, Pena-Shokeir syndrome, multiple congenital arthrogryposis and/or short umbilical cord: conceptual delimitation]. Gonzalez de Dios J; García-Alix A An Esp Pediatr; 1998 Feb; 48(2):197-200. PubMed ID: 9577032 [No Abstract] [Full Text] [Related]
18. Surgical treatment of choanal atresia in CHARGE association: case report with long-term follow-up. Carinci F; Hassanipour A; Mandrioli S; Pastore A J Craniomaxillofac Surg; 1999 Oct; 27(5):321-6. PubMed ID: 10717836 [TBL] [Abstract][Full Text] [Related]
19. Bilateral microtia with severe cardiac defect: a new syndrome, or a severe manifestation of the oculoauriculovertebral spectrum? McKee S; Mabrouk R; Bali S Clin Dysmorphol; 2006 Apr; 15(2):121-2. PubMed ID: 16531742 [TBL] [Abstract][Full Text] [Related]