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4. The forkhead/winged helix gene Mf1 is disrupted in the pleiotropic mouse mutation congenital hydrocephalus. Kume T; Deng KY; Winfrey V; Gould DB; Walter MA; Hogan BL Cell; 1998 Jun; 93(6):985-96. PubMed ID: 9635428 [TBL] [Abstract][Full Text] [Related]
5. Pleiotropic skeletal and ocular phenotypes of the mouse mutation congenital hydrocephalus (ch/Mf1) arise from a winged helix/forkhead transcriptionfactor gene. Hong HK; Lass JH; Chakravarti A Hum Mol Genet; 1999 Apr; 8(4):625-37. PubMed ID: 10072431 [TBL] [Abstract][Full Text] [Related]
6. The role of genetics in understanding hydrocephalus and spina bifida. An update. Jouet M Eur J Pediatr Surg; 1996 Dec; 6 Suppl 1():35-6. PubMed ID: 9008819 [No Abstract] [Full Text] [Related]
7. Genetics of human hydrocephalus. Zhang J; Williams MA; Rigamonti D J Neurol; 2006 Oct; 253(10):1255-66. PubMed ID: 16773266 [TBL] [Abstract][Full Text] [Related]
8. A mutation in the general membrane trafficking machinery and hydrocephaly. Söllner TH Proc Natl Acad Sci U S A; 2004 Feb; 101(6):1431-2. PubMed ID: 14757810 [No Abstract] [Full Text] [Related]
10. Genetics and Molecular Pathogenesis of Human Hydrocephalus. Garcia-Bonilla M; McAllister JP; Limbrick DD Neurol India; 2021; 69(Supplement):S268-S274. PubMed ID: 35102976 [TBL] [Abstract][Full Text] [Related]
11. Genes causing congenital hydrocephalus: Their chromosomal characteristics of telomere proximity and DNA compositions. McKnight I; Hart C; Park IH; Shim JW Exp Neurol; 2021 Jan; 335():113523. PubMed ID: 33157092 [TBL] [Abstract][Full Text] [Related]
12. A homozygous frameshift variant in an alternatively spliced exon of DLG5 causes hydrocephalus and renal dysplasia. Yüksel Z; Vogel F; Alhashem AM; Alanzi TSA; Tabarki B; Kampe K; Kandaswamy KK; Werber M; Bertoli-Avella AM; Beetz C; Rolfs A; Bauer P Clin Genet; 2019 May; 95(5):631-633. PubMed ID: 30791088 [No Abstract] [Full Text] [Related]
13. [Importance of the clinical genetics evaluation on hydrocephalus]. Wey-Vieira M; Cavalcanti DP; Lopes VL Arq Neuropsiquiatr; 2004 Jun; 62(2B):480-6. PubMed ID: 15273848 [TBL] [Abstract][Full Text] [Related]
14. Trafficking in cell fate. Bajjalieh S Nat Genet; 2004 Mar; 36(3):216-7. PubMed ID: 14988718 [No Abstract] [Full Text] [Related]
15. Mutation in MPDZ causes severe congenital hydrocephalus. Al-Dosari MS; Al-Owain M; Tulbah M; Kurdi W; Adly N; Al-Hemidan A; Masoodi TA; Albash B; Alkuraya FS J Med Genet; 2013 Jan; 50(1):54-8. PubMed ID: 23240096 [TBL] [Abstract][Full Text] [Related]
16. Visualizing flow in an intact CSF network using optical coherence tomography: implications for human congenital hydrocephalus. Date P; Ackermann P; Furey C; Fink IB; Jonas S; Khokha MK; Kahle KT; Deniz E Sci Rep; 2019 Apr; 9(1):6196. PubMed ID: 30996265 [TBL] [Abstract][Full Text] [Related]
17. Compound variants of FKTN, POMGNT1, and LAMB1 gene identified by prenatal whole-exome sequencing in three fetuses with congenital hydrocephalus. Li M; Fu H; Li J; Meng D; Zhang Q; Fei D J Obstet Gynaecol Res; 2022 Oct; 48(10):2624-2629. PubMed ID: 35843586 [TBL] [Abstract][Full Text] [Related]
18. SMARCC1 is a susceptibility gene for congenital hydrocephalus with an autosomal dominant inheritance mode and incomplete penetrance. Hourvitz N; Kurolap A; Mory A; Haratz KK; Kidron D; Malinger G; Baris Feldman H; Yaron Y Prenat Diagn; 2023 Sep; 43(10):1374-1377. PubMed ID: 37639281 [TBL] [Abstract][Full Text] [Related]