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.
5. The identification of a novel locus for mandibular prognathism in the Han Chinese population. Li Q; Li X; Zhang F; Chen F J Dent Res; 2011 Jan; 90(1):53-7. PubMed ID: 21041550 [TBL] [Abstract][Full Text] [Related]
6. On the genetics of mandibular prognathism: analysis of large European noble families. Wolff G; Wienker TF; Sander H J Med Genet; 1993 Feb; 30(2):112-6. PubMed ID: 8445614 [TBL] [Abstract][Full Text] [Related]
8. Mental retardation, obesity, mandibular prognathism with eye and skin anomalies (MOMES syndrome): a newly recognized autosomal recessive syndrome. Kantaputra PN; Kunachaichote J; Patikulsila P Am J Med Genet; 2001 Nov; 103(4):283-8. PubMed ID: 11746007 [TBL] [Abstract][Full Text] [Related]
9. Microsatellite genome-wide association study for mandibular prognathism. Ikuno K; Kajii TS; Oka A; Inoko H; Ishikawa H; Iida J Am J Orthod Dentofacial Orthop; 2014 Jun; 145(6):757-62. PubMed ID: 24880846 [TBL] [Abstract][Full Text] [Related]
10. Polymorphisms in the Matrilin-1 gene and risk of mandibular prognathism in Koreans. Jang JY; Park EK; Ryoo HM; Shin HI; Kim TH; Jang JS; Park HS; Choi JY; Kwon TG J Dent Res; 2010 Nov; 89(11):1203-7. PubMed ID: 20739701 [TBL] [Abstract][Full Text] [Related]
11. [Genetic determination and mode of transmission of mandibular prognathism]. Mauchamp OP Orthod Fr; 1974; 45(2):143-54. PubMed ID: 4534498 [No Abstract] [Full Text] [Related]
12. Mandibular prognathism in Japanese families ascertained through orthognathically treated patients. Watanabe M; Suda N; Ohyama K Am J Orthod Dentofacial Orthop; 2005 Oct; 128(4):466-70. PubMed ID: 16214628 [TBL] [Abstract][Full Text] [Related]
13. [Problems and methodology of human genetic research in the scope of orthodontics--3]. Schulze C Dtsch Zahnarztl Z; 1973 May; 28(5):570-9. PubMed ID: 4513565 [No Abstract] [Full Text] [Related]
14. Identification of a Mutation in FGF23 Involved in Mandibular Prognathism. Chen F; Li Q; Gu M; Li X; Yu J; Zhang YB Sci Rep; 2015 Jun; 5():11250. PubMed ID: 26059428 [TBL] [Abstract][Full Text] [Related]
15. Genetic Etiology in Nonsyndromic Mandibular Prognathism. Liu H; Wu C; Lin J; Shao J; Chen Q; Luo E J Craniofac Surg; 2017 Jan; 28(1):161-169. PubMed ID: 27941554 [TBL] [Abstract][Full Text] [Related]
16. Evidence of mendelian inheritance of the nucleolar organizer regions in the Spanish common rabbit. Arruga MV; Monteagudo LV J Hered; 1989; 80(1):85-6. PubMed ID: 2921512 [No Abstract] [Full Text] [Related]
17. Genetic deficiency of the alpha-gamma-subunit of the eighth complement component in the rabbit. Komatsu M; Yamamoto K; Kawashima T; Migita S J Immunol; 1985 Apr; 134(4):2607-9. PubMed ID: 3973389 [TBL] [Abstract][Full Text] [Related]
18. [Mandibular prognathism in identical twins: case report]. Reyes JT; Miguel JL; Cienfuegos ES Quintessencia; 1982 May; 9(5):25-9. PubMed ID: 6963421 [No Abstract] [Full Text] [Related]
19. Analysis of the association of COL2A1 and IGF-1 with mandibular prognathism in a Chinese population. Xue F; Rabie AB; Luo G Orthod Craniofac Res; 2014 Aug; 17(3):144-9. PubMed ID: 24386886 [TBL] [Abstract][Full Text] [Related]
20. Hereditary macrostomus in the rabbit: a model for Treacher Collins syndrome, one form of mandibulofacial dysostosis. Fox RR; Crary DD J Hered; 1979; 70(6):369-72. PubMed ID: 544686 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]