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4. Identification of new candidate genes for spina bifida through exome sequencing. Azzarà A; Rendeli C; Crivello AM; Brugnoletti F; Rumore R; Ausili E; Sangiorgi E; Gurrieri F Childs Nerv Syst; 2021 Aug; 37(8):2589-2596. PubMed ID: 33855610 [TBL] [Abstract][Full Text] [Related]
5. TRIM4 is associated with neural tube defects based on genome-wide DNA methylation analysis. Zhang H; Guo Y; Gu H; Wei X; Ma W; Liu D; Yu K; Luo W; Ma L; Liu Y; Xue J; Huang J; Wang Y; Jia S; Dong N; Wang H; Yuan Z Clin Epigenetics; 2019 Feb; 11(1):17. PubMed ID: 30709423 [TBL] [Abstract][Full Text] [Related]
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7. Exome versus transcriptome sequencing in identifying coding region variants. Ku CS; Wu M; Cooper DN; Naidoo N; Pawitan Y; Pang B; Iacopetta B; Soong R Expert Rev Mol Diagn; 2012 Apr; 12(3):241-51. PubMed ID: 22468815 [TBL] [Abstract][Full Text] [Related]
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9. Loss-of-function de novo mutations play an important role in severe human neural tube defects. Lemay P; Guyot MC; Tremblay É; Dionne-Laporte A; Spiegelman D; Henrion É; Diallo O; De Marco P; Merello E; Massicotte C; Désilets V; Michaud JL; Rouleau GA; Capra V; Kibar Z J Med Genet; 2015 Jul; 52(7):493-7. PubMed ID: 25805808 [TBL] [Abstract][Full Text] [Related]
10. Genome-wide association mapping in dogs enables identification of the homeobox gene, NKX2-8, as a genetic component of neural tube defects in humans. Safra N; Bassuk AG; Ferguson PJ; Aguilar M; Coulson RL; Thomas N; Hitchens PL; Dickinson PJ; Vernau KM; Wolf ZT; Bannasch DL PLoS Genet; 2013; 9(7):e1003646. PubMed ID: 23874236 [TBL] [Abstract][Full Text] [Related]
12. Exome analysis in an Estonian multiplex family with neural tube defects-a case report. Pappa L; Kals M; Kivistik PA; Metspalu A; Paal A; Nikopensius T Childs Nerv Syst; 2017 Sep; 33(9):1575-1581. PubMed ID: 28721594 [TBL] [Abstract][Full Text] [Related]
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18. Genetic backgrounds and modifier genes of NTD mouse models: An opportunity for greater understanding of the multifactorial etiology of neural tube defects. Leduc RY; Singh P; McDermid HE Birth Defects Res; 2017 Jan; 109(2):140-152. PubMed ID: 27768235 [TBL] [Abstract][Full Text] [Related]
19. Approaches to studying the genomic architecture of complex birth defects. Taiwo TE; Cao X; Cabrera RM; Lei Y; Finnell RH Prenat Diagn; 2020 Aug; 40(9):1047-1055. PubMed ID: 32468575 [TBL] [Abstract][Full Text] [Related]
20. Developments in our understanding of the genetic basis of birth defects. Webber DM; MacLeod SL; Bamshad MJ; Shaw GM; Finnell RH; Shete SS; Witte JS; Erickson SW; Murphy LD; Hobbs C Birth Defects Res A Clin Mol Teratol; 2015 Aug; 103(8):680-91. PubMed ID: 26033863 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]