85 related articles for article (PubMed ID: 12432504)
41. Differential parental transmission of markers in BCL3 among Korean cleft case-parent trios.
Park BY; Sull JW; Park JY; Jee SH; Beaty TH
J Prev Med Public Health; 2009 Jan; 42(1):1-4. PubMed ID: 19229118
[TBL] [Abstract][Full Text] [Related]
42. Orofacial clefting: update on the role of genetics.
Ghassibe M; Bayet B; Revencu N; Desmyter L; Verellen-Dumoulin C; Gillerot Y; Deggouj N; Vanwijck R; Vikkula M;
B-ENT; 2006; 2 Suppl 4():20-4. PubMed ID: 17366841
[TBL] [Abstract][Full Text] [Related]
43. A case-control study of nonsyndromic oral clefts in Maryland.
Beaty TH; Wang H; Hetmanski JB; Fan YT; Zeiger JS; Liang KY; Chiu YF; Vanderkolk CA; Seifert KC; Wulfsberg EA; Raymond G; Panny SR; McIntosh I
Ann Epidemiol; 2001 Aug; 11(6):434-42. PubMed ID: 11454503
[TBL] [Abstract][Full Text] [Related]
44. [Association study on microsatellite polymorphisms of MSX1 gene and nonsyndromic cleft lip and palate].
Wu PA; Li YL; Fan GZ; Wang K
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Jun; 24(3):325-7. PubMed ID: 17557248
[TBL] [Abstract][Full Text] [Related]
45. Orofacial cleft defects: inference from nature and nurture.
Houdayer C; Bahuau M
Ann Genet; 1998; 41(2):89-117. PubMed ID: 9706339
[TBL] [Abstract][Full Text] [Related]
46. Clinical relevance of breast and gastric cancer-associated polymorphisms as potential susceptibility markers for oral clefts in the Brazilian population.
Machado RA; de Freitas EM; de Aquino SN; Martelli DR; Swerts MS; Reis SR; Persuhn DC; Moreira HS; Dias VO; Coletta RD; Martelli-Júnior H
BMC Med Genet; 2017 Apr; 18(1):39. PubMed ID: 28376813
[TBL] [Abstract][Full Text] [Related]
47. Cleft palate, transforming growth factor alpha gene variants, and maternal exposures: assessing gene-environment interactions in case-parent triads.
Jugessur A; Lie RT; Wilcox AJ; Murray JC; Taylor JA; Saugstad OD; Vindenes HA; Abyholm FE
Genet Epidemiol; 2003 Dec; 25(4):367-74. PubMed ID: 14639706
[TBL] [Abstract][Full Text] [Related]
48. Rare Variants in the Epithelial Cadherin Gene Underlying the Genetic Etiology of Nonsyndromic Cleft Lip with or without Cleft Palate.
Brito LA; Yamamoto GL; Melo S; Malcher C; Ferreira SG; Figueiredo J; Alvizi L; Kobayashi GS; Naslavsky MS; Alonso N; Felix TM; Zatz M; Seruca R; Passos-Bueno MR
Hum Mutat; 2015 Nov; 36(11):1029-33. PubMed ID: 26123647
[TBL] [Abstract][Full Text] [Related]
49. Linkage analysis of candidate endothelin pathway genes in nonsyndromic familial orofacial cleft.
Pezzetti F; Scapoli L; Martinelli M; Carinci F; Brunelli G; Carls FP; Palomba F; Gombos F; Carinci P; Tognon M
Ann Hum Genet; 2000 Jul; 64(Pt 4):341-7. PubMed ID: 11415518
[TBL] [Abstract][Full Text] [Related]
50. The common MTHFR C677T and A1298C variants are not associated with the risk of non-syndromic cleft lip/palate in northern Venezuela.
Sözen MA; Tolarova MM; Spritz RA
J Genet Genomics; 2009 May; 36(5):283-8. PubMed ID: 19447376
[TBL] [Abstract][Full Text] [Related]
51. Novel insertion mutation in the PVRL1 gene in Turkish patients with non-syndromic cleft lip with/without cleft palate.
Aşlar D; Taştan H
Arch Oral Biol; 2014 Mar; 59(3):237-40. PubMed ID: 24581844
[TBL] [Abstract][Full Text] [Related]
52. Segregation of HLA in families with oral clefts: evidence against linkage between isolated cleft palate and HLA.
Van Dyke DC; Goldman AS; Spielman RS; Zmijewski CM
Am J Med Genet; 1983 May; 15(1):85-8. PubMed ID: 6859128
[TBL] [Abstract][Full Text] [Related]
53. DLX1 and MMP3 contribute to oral clefts with and without positive family history of cancer.
Sabóia TM; Reis MF; Martins ÂM; Romanos HF; Tannure PN; Granjeiro JM; Vieira AR; Antunes LS; Küchler EC; Costa MC
Arch Oral Biol; 2015 Feb; 60(2):223-8. PubMed ID: 25463899
[TBL] [Abstract][Full Text] [Related]
54. Nonsyndromic cleft lip with or without cleft palate: new BCL3 information.
Amos C; Gasser D; Hecht JT
Am J Hum Genet; 1996 Sep; 59(3):743-4. PubMed ID: 8751880
[No Abstract] [Full Text] [Related]
55. Suggestive linkage between markers on chromosome 19q13.2 and nonsyndromic orofacial cleft malformation.
Martinelli M; Scapoli L; Pezzetti F; Carinci F; Carinci P; Baciliero U; Padula E; Tognon M
Genomics; 1998 Jul; 51(2):177-81. PubMed ID: 9722939
[TBL] [Abstract][Full Text] [Related]
56. Linkage analysis between BCL3 and nearby genes on 19q13.2 and non-syndromic cleft lip with or without cleft palate in multigenerational Japanese families.
Fujita H; Nagata M; Ono K; Okubo H; Takagi R
Oral Dis; 2004 Nov; 10(6):353-9. PubMed ID: 15533211
[TBL] [Abstract][Full Text] [Related]
57. MSX1 gene and nonsyndromic oral clefts in a Southern Brazilian population.
Souza LT; Kowalski TW; Collares MV; Félix TM
Braz J Med Biol Res; 2013 Jul; 46(7):555-8. PubMed ID: 23903689
[TBL] [Abstract][Full Text] [Related]
58. Frequency of cancer in first-degree relatives of patients with cleft lip and/or palate in the Brazilian population.
Lima LS; Silvério Mde O; Swerts MS; Aquino SN; Martelli DR; Martelli-Júnior H
Braz Dent J; 2013; 24(3):200-3. PubMed ID: 23969906
[TBL] [Abstract][Full Text] [Related]
59. [Association between cleft lip/palate phenotype and non syndrome microsatellite markers located in 6p, 17q and 19q].
Carreño H; Suazo J; Paredes M; Solá J; Valenzuela J; Blanco R
Rev Med Chil; 2002 Jan; 130(1):35-44. PubMed ID: 11961959
[TBL] [Abstract][Full Text] [Related]
60. MSX ₁ gene variant and non-syndromic clefting: association or rejection?
Reddy NA; Gopinath A; Reddy JT; Devanna R; Saravanan P; Rohra MG
Indian J Dent Res; 2014; 25(1):45-9. PubMed ID: 24748298
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
