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.
22. Strømme Syndrome Is a Ciliary Disorder Caused by Mutations in CENPF. Filges I; Bruder E; Brandal K; Meier S; Undlien DE; Waage TR; Hoesli I; Schubach M; de Beer T; Sheng Y; Hoeller S; Schulzke S; Røsby O; Miny P; Tercanli S; Oppedal T; Meyer P; Selmer KK; Strømme P Hum Mutat; 2016 Apr; 37(4):359-63. PubMed ID: 26820108 [TBL] [Abstract][Full Text] [Related]
23. DYNC2H1 mutation causes Jeune syndrome and recurrent lung infections associated with ciliopathy. Emiralioglu N; Wallmeier J; Olbrich H; Omran H; Ozcelik U Clin Respir J; 2018 Mar; 12(3):1017-1020. PubMed ID: 28257607 [TBL] [Abstract][Full Text] [Related]
24. IFT80 mutations cause a novel complex ciliopathy phenotype with retinal degeneration. Moran J; G Sanderson K; Maynes J; Vig A; Batmanabane V; Kannu P; Tavares E; Vincent A; Héon E Clin Genet; 2018 Oct; 94(3-4):368-372. PubMed ID: 29923190 [TBL] [Abstract][Full Text] [Related]
25. Novel compound heterozygous mutations in DYNC2H1 in a patient with severe short-rib polydactyly syndrome type III phenotype. Okamoto T; Nagaya K; Kawata Y; Asai H; Tsuchida E; Nohara F; Okajima K; Azuma H Congenit Anom (Kyoto); 2015 Aug; 55(3):155-7. PubMed ID: 25410398 [TBL] [Abstract][Full Text] [Related]
26. Mutations in ARMC9, which Encodes a Basal Body Protein, Cause Joubert Syndrome in Humans and Ciliopathy Phenotypes in Zebrafish. Van De Weghe JC; Rusterholz TDS; Latour B; Grout ME; Aldinger KA; Shaheen R; Dempsey JC; Maddirevula S; Cheng YH; Phelps IG; Gesemann M; Goel H; Birk OS; Alanzi T; Rawashdeh R; Khan AO; ; Bamshad MJ; Nickerson DA; Neuhauss SCF; Dobyns WB; Alkuraya FS; Roepman R; Bachmann-Gagescu R; Doherty D Am J Hum Genet; 2017 Jul; 101(1):23-36. PubMed ID: 28625504 [TBL] [Abstract][Full Text] [Related]
27. CiliOPD: a ciliopathy-associated COPD endotype. Perotin JM; Polette M; Deslée G; Dormoy V Respir Res; 2021 Feb; 22(1):74. PubMed ID: 33639936 [TBL] [Abstract][Full Text] [Related]
28. Compound heterozygous mutations in the IFT140 gene cause Opitz trigonocephaly C syndrome in a patient with typical features of a ciliopathy. Peña-Padilla C; Marshall CR; Walker S; Scherer SW; Tavares-Macías G; Razo-Jiménez G; Bobadilla-Morales L; Acosta-Fernández E; Corona-Rivera A; Mendoza-Londono R; Corona-Rivera JR Clin Genet; 2017 Apr; 91(4):640-646. PubMed ID: 27874174 [TBL] [Abstract][Full Text] [Related]
29. Expanding the phenotype of CRB2 mutations - A new ciliopathy syndrome? Jaron R; Rosenfeld N; Zahdeh F; Carmi S; Beni-Adani L; Doviner V; Picard E; Segel R; Zeligson S; Carmel L; Renbaum P; Levy-Lahad E Clin Genet; 2016 Dec; 90(6):540-544. PubMed ID: 26925547 [TBL] [Abstract][Full Text] [Related]
30. Beemer-Langer syndrome is a ciliopathy due to biallelic mutations in IFT122. Silveira KC; Moreno CA; Cavalcanti DP Am J Med Genet A; 2017 May; 173(5):1186-1189. PubMed ID: 28370949 [TBL] [Abstract][Full Text] [Related]
31. Confirming TBC1D32-related ciliopathy in humans. Alsahan N; Alkuraya FS Am J Med Genet A; 2020 Aug; 182(8):1985-1987. PubMed ID: 32573025 [No Abstract] [Full Text] [Related]
32. Whole exome sequencing is an efficient, sensitive and specific method for determining the genetic cause of short-rib thoracic dystrophies. McInerney-Leo AM; Harris JE; Leo PJ; Marshall MS; Gardiner B; Kinning E; Leong HY; McKenzie F; Ong WP; Vodopiutz J; Wicking C; Brown MA; Zankl A; Duncan EL Clin Genet; 2015 Dec; 88(6):550-7. PubMed ID: 25492405 [TBL] [Abstract][Full Text] [Related]
33. Copy number variations and multiallelic variants in Korean patients with Leber congenital amaurosis. Surl D; Shin S; Lee ST; Choi JR; Lee J; Byeon SH; Han SH; Lim HT; Han J Mol Vis; 2020; 26():26-35. PubMed ID: 32165824 [TBL] [Abstract][Full Text] [Related]
35. Currarino syndrome: variable imaging features in three siblings with HLXB9 gene mutation. Kim AY; Yoo SY; Kim JH; Eo H; Jeon TY Clin Imaging; 2013; 37(2):398-402. PubMed ID: 23466002 [TBL] [Abstract][Full Text] [Related]
36. Targeted exome sequencing resolves allelic and the genetic heterogeneity in the genetic diagnosis of nephronophthisis-related ciliopathy. Kang HG; Lee HK; Ahn YH; Joung JG; Nam J; Kim NK; Ko JM; Cho MH; Shin JI; Kim J; Park HW; Park YS; Ha IS; Chung WY; Lee DY; Kim SY; Park WY; Cheong HI Exp Mol Med; 2016 Aug; 48(8):e251. PubMed ID: 27491411 [TBL] [Abstract][Full Text] [Related]
37. Molecular Study of Nephronophthisis in 7 Unrelated Pakistani Families. Hussain S; Akhtar N; Qamar R; Khan N; Naeem M Iran J Kidney Dis; 2018 Jul; 12(4):240-242. PubMed ID: 30087219 [TBL] [Abstract][Full Text] [Related]
38. X-linked VACTERL-H caused by deletion of exon 3 in FANCB: A case report. Watanabe N; Tsutsumi S; Miyano Y; Sato H; Nagase S Congenit Anom (Kyoto); 2018 Sep; 58(5):171-172. PubMed ID: 29232005 [No Abstract] [Full Text] [Related]
39. Clinical and genetic differences in total colonic aganglionosis in Hirschsprung's disease. Moore SW; Zaahl M J Pediatr Surg; 2009 Oct; 44(10):1899-903. PubMed ID: 19853744 [TBL] [Abstract][Full Text] [Related]
40. Whole exome sequencing as a diagnostic tool for patients with ciliopathy-like phenotypes. Castro-Sánchez S; Álvarez-Satta M; Tohamy MA; Beltran S; Derdak S; Valverde D PLoS One; 2017; 12(8):e0183081. PubMed ID: 28800606 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]