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.
435 related articles for article (PubMed ID: 29500247)
1. Whole exome sequencing identifies mutations in 10% of patients with familial non-syndromic cleft lip and/or palate in genes mutated in well-known syndromes. Basha M; Demeer B; Revencu N; Helaers R; Theys S; Bou Saba S; Boute O; Devauchelle B; Francois G; Bayet B; Vikkula M J Med Genet; 2018 Jul; 55(7):449-458. PubMed ID: 29500247 [TBL] [Abstract][Full Text] [Related]
2. Association study between Van der Woude Syndrome causative gene GRHL3 and nonsyndromic cleft lip with or without cleft palate in a Chinese cohort. Wang Y; Sun Y; Huang Y; Pan Y; Jia Z; Ma L; Ma L; Lan F; Zhou Y; Shi J; Yang X; Zhang L; Jiang H; Jiang M; Yin A; Cheng J; Wang L; Yang Y; Shi B Gene; 2016 Aug; 588(1):69-73. PubMed ID: 27129939 [TBL] [Abstract][Full Text] [Related]
3. Sequencing the GRHL3 Coding Region Reveals Rare Truncating Mutations and a Common Susceptibility Variant for Nonsyndromic Cleft Palate. Mangold E; Böhmer AC; Ishorst N; Hoebel AK; Gültepe P; Schuenke H; Klamt J; Hofmann A; Gölz L; Raff R; Tessmann P; Nowak S; Reutter H; Hemprich A; Kreusch T; Kramer FJ; Braumann B; Reich R; Schmidt G; Jäger A; Reiter R; Brosch S; Stavusis J; Ishida M; Seselgyte R; Moore GE; Nöthen MM; Borck G; Aldhorae KA; Lace B; Stanier P; Knapp M; Ludwig KU Am J Hum Genet; 2016 Apr; 98(4):755-62. PubMed ID: 27018475 [TBL] [Abstract][Full Text] [Related]
4. Identification of a novel TP63 mutation causing nonsyndromic cleft lip with or without cleft palate. Xu T; Du M; Bu X; Yuan D; Gu Z; Yu P; Li X; Chen J; Jin C BMC Med Genomics; 2021 Feb; 14(1):53. PubMed ID: 33622322 [TBL] [Abstract][Full Text] [Related]
5. Identification of a Novel Variant of Tang JX; Xiao XS; Wang K; Jin JY; Fan LL; Xiang R Biomed Res Int; 2020; 2020():8790531. PubMed ID: 33150183 [TBL] [Abstract][Full Text] [Related]
6. Three GLI2 mutations combined potentially underlie non-syndromic cleft lip with or without cleft palate in a Chinese pedigree. Meng P; Zhao H; Huang W; Zhang Y; Zhong W; Zhang M; Jia P; Zhou Z; Maimaitili G; Chen F; Zhang J; Lin J Mol Genet Genomic Med; 2019 Sep; 7(9):e714. PubMed ID: 31386309 [TBL] [Abstract][Full Text] [Related]
7. Association studies of low-frequency coding variants in nonsyndromic cleft lip with or without cleft palate. Leslie EJ; Carlson JC; Shaffer JR; Buxó CJ; Castilla EE; Christensen K; Deleyiannis FWB; Field LL; Hecht JT; Moreno L; Orioli IM; Padilla C; Vieira AR; Wehby GL; Feingold E; Weinberg SM; Murray JC; Marazita ML Am J Med Genet A; 2017 Jun; 173(6):1531-1538. PubMed ID: 28425186 [TBL] [Abstract][Full Text] [Related]
8. IRF6 mutation screening in non-syndromic orofacial clefting: analysis of 1521 families. Leslie EJ; Koboldt DC; Kang CJ; Ma L; Hecht JT; Wehby GL; Christensen K; Czeizel AE; Deleyiannis FW; Fulton RS; Wilson RK; Beaty TH; Schutte BC; Murray JC; Marazita ML Clin Genet; 2016 Jul; 90(1):28-34. PubMed ID: 26346622 [TBL] [Abstract][Full Text] [Related]
9. Identifying Genetic Sources of Phenotypic Heterogeneity in Orofacial Clefts by Targeted Sequencing. Carlson JC; Taub MA; Feingold E; Beaty TH; Murray JC; Marazita ML; Leslie EJ Birth Defects Res; 2017 Jul; 109(13):1030-1038. PubMed ID: 28762674 [TBL] [Abstract][Full Text] [Related]
10. Mutations in the Epithelial Cadherin-p120-Catenin Complex Cause Mendelian Non-Syndromic Cleft Lip with or without Cleft Palate. Cox LL; Cox TC; Moreno Uribe LM; Zhu Y; Richter CT; Nidey N; Standley JM; Deng M; Blue E; Chong JX; Yang Y; Carstens RP; Anand D; Lachke SA; Smith JD; Dorschner MO; Bedell B; Kirk E; Hing AV; Venselaar H; Valencia-Ramirez LC; Bamshad MJ; Glass IA; Cooper JA; Haan E; Nickerson DA; van Bokhoven H; Zhou H; Krahn KN; Buckley MF; Murray JC; Lidral AC; Roscioli T Am J Hum Genet; 2018 Jun; 102(6):1143-1157. PubMed ID: 29805042 [TBL] [Abstract][Full Text] [Related]
11. [Exploring the association between Chen X; Wang SY; Xue EC; Wang XH; Peng HX; Fan M; Wang MY; Wu YQ; Qin XY; Li J; Wu T; Zhu HP; Li J; Zhou ZB; Chen DF; Hu YH Beijing Da Xue Xue Bao Yi Xue Ban; 2022 Jun; 54(3):387-393. PubMed ID: 35701113 [TBL] [Abstract][Full Text] [Related]
12. Van der Woude and Popliteal Pterygium Syndromes: Broad intrafamilial variability in a three generation family with mutation in IRF6. Busche A; Hehr U; Sieg P; Gillessen-Kaesbach G Am J Med Genet A; 2016 Sep; 170(9):2404-7. PubMed ID: 27286731 [TBL] [Abstract][Full Text] [Related]
13. Gene-gene interaction of single nucleotide polymorphisms in 16p13.3 may contribute to the risk of non-syndromic cleft lip with or without cleft palate in Chinese case-parent trios. Liu D; Wang H; Schwender H; Marazita ML; Wang Z; Yuan Y; Wang P; Liang KY; Wu-Chou YH; Wang M; Shi B; Zhu H; Wu T; Beaty TH Am J Med Genet A; 2017 Jun; 173(6):1489-1494. PubMed ID: 28402597 [TBL] [Abstract][Full Text] [Related]
14. Possible relationship between the van der Woude syndrome (vWS) locus and nonsyndromic cleft lip with or without cleft palate (NSCL/P). Houdayer C; Bonaïti-Pellié C; Erguy C; Soupre V; Dondon MG; Bürglen L; Cougoureux E; Couderc R; Vazquez MP; Bahuau M Am J Med Genet; 2001 Nov; 104(1):86-92. PubMed ID: 11746036 [TBL] [Abstract][Full Text] [Related]
15. Analysis of the p63 gene in classical EEC syndrome, related syndromes, and non-syndromic orofacial clefts. Barrow LL; van Bokhoven H; Daack-Hirsch S; Andersen T; van Beersum SE; Gorlin R; Murray JC J Med Genet; 2002 Aug; 39(8):559-66. PubMed ID: 12161593 [TBL] [Abstract][Full Text] [Related]
16. Using whole exome sequencing to identify susceptibility genes associated with nonsyndromic cleft lip with or without cleft palate. Fu Z; Yue J; Xue L; Xu Y; Ding Q; Xiao W Mol Genet Genomics; 2023 Jan; 298(1):107-118. PubMed ID: 36322204 [TBL] [Abstract][Full Text] [Related]
17. Irf6 directly regulates Klf17 in zebrafish periderm and Klf4 in murine oral epithelium, and dominant-negative KLF4 variants are present in patients with cleft lip and palate. Liu H; Leslie EJ; Jia Z; Smith T; Eshete M; Butali A; Dunnwald M; Murray J; Cornell RA Hum Mol Genet; 2016 Feb; 25(4):766-76. PubMed ID: 26692521 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. A Novel Du S; Yang Y; Yi P; Luo J; Liu T; Chen R; Liu CJ; Ma T; Li Y; Wang C; Weng J; Liu M; Zhang L; Yang B; Zeng X; Liu JY Genet Test Mol Biomarkers; 2019 Nov; 23(11):759-765. PubMed ID: 31638429 [No Abstract] [Full Text] [Related] [Next] [New Search]