178 related articles for article (PubMed ID: 15547403)
21. The mapping of a gene for craniosynostosis: evidence for linkage of the Saethre-Chotzen syndrome to distal chromosome 7p.
Brueton LA; van Herwerden L; Chotai KA; Winter RM
J Med Genet; 1992 Oct; 29(10):681-5. PubMed ID: 1433226
[TBL] [Abstract][Full Text] [Related]
22. A comprehensive screen for TWIST mutations in patients with craniosynostosis identifies a new microdeletion syndrome of chromosome band 7p21.1.
Johnson D; Horsley SW; Moloney DM; Oldridge M; Twigg SR; Walsh S; Barrow M; Njølstad PR; Kunz J; Ashworth GJ; Wall SA; Kearney L; Wilkie AO
Am J Hum Genet; 1998 Nov; 63(5):1282-93. PubMed ID: 9792856
[TBL] [Abstract][Full Text] [Related]
23. Translocation breakpoint maps 5 kb 3' from TWIST in a patient affected with Saethre-Chotzen syndrome.
Krebs I; Weis I; Hudler M; Rommens JM; Roth H; Scherer SW; Tsui LC; Füchtbauer EM; Grzeschik KH; Tsuji K; Kunz J
Hum Mol Genet; 1997 Jul; 6(7):1079-86. PubMed ID: 9215678
[TBL] [Abstract][Full Text] [Related]
24. Pharmacological targeting of KDM6A and KDM6B, as a novel therapeutic strategy for treating craniosynostosis in Saethre-Chotzen syndrome.
Pribadi C; Camp E; Cakouros D; Anderson P; Glackin C; Gronthos S
Stem Cell Res Ther; 2020 Dec; 11(1):529. PubMed ID: 33298158
[TBL] [Abstract][Full Text] [Related]
25. A child with Saethre-Chotzen syndrome, sensorineural hearing loss, and a TWIST mutation.
Lee S; Seto M; Sie K; Cunningham M
Cleft Palate Craniofac J; 2002 Jan; 39(1):110-4. PubMed ID: 11772178
[TBL] [Abstract][Full Text] [Related]
26. Genetic heterogeneity among craniosynostosis syndromes: mapping the Saethre-Chotzen syndrome locus between D7S513 and D7S516 and exclusion of Jackson-Weiss and Crouzon syndrome loci from 7p.
Lewanda AF; Cohen MM; Jackson CE; Taylor EW; Li X; Beloff M; Day D; Clarren SK; Ortiz R; Garcia C
Genomics; 1994 Jan; 19(1):115-9. PubMed ID: 8188211
[TBL] [Abstract][Full Text] [Related]
27. Interrelationship of cranial suture fusion, basicranial development, and resynostosis following suturectomy in twist1(+/-) mice, a murine model of Saethre-Chotzen syndrome.
Hermann CD; Lee CS; Gadepalli S; Lawrence KA; Richards MA; Olivares-Navarrete R; Williams JK; Schwartz Z; Boyan BD
Calcif Tissue Int; 2012 Oct; 91(4):255-66. PubMed ID: 22903506
[TBL] [Abstract][Full Text] [Related]
28. TWIST microdeletion identified by array CGH in a patient presenting Saethre-Chotzen phenotype and a complex rearrangement involving chromosomes 2 and 7.
Schluth-Bolard C; Till M; Labalme A; Rey C; Banquart E; Fautrelle A; Martin-Denavit T; Le Lorc'h M; Romana SP; Lazar V; Edery P; Sanlaville D
Eur J Med Genet; 2008; 51(2):156-64. PubMed ID: 18255367
[TBL] [Abstract][Full Text] [Related]
29. Reoperation for intracranial hypertension in TWIST1-confirmed Saethre-Chotzen syndrome: a 15-year review.
Woods RH; Ul-Haq E; Wilkie AOM; Jayamohan J; Richards PG; Johnson D; Lester T; Wall SA
Plast Reconstr Surg; 2009 Jun; 123(6):1801-1810. PubMed ID: 19483581
[TBL] [Abstract][Full Text] [Related]
30. The natural history of patients treated for TWIST1-confirmed Saethre-Chotzen syndrome.
Foo R; Guo Y; McDonald-McGinn DM; Zackai EH; Whitaker LA; Bartlett SP
Plast Reconstr Surg; 2009 Dec; 124(6):2085-2095. PubMed ID: 19952666
[TBL] [Abstract][Full Text] [Related]
31. Saethre-Chotzen syndrome: review of the literature and report of a case.
Clauser L; Galiè M; Hassanipour A; Calabrese O
J Craniofac Surg; 2000 Sep; 11(5):480-6. PubMed ID: 11314068
[TBL] [Abstract][Full Text] [Related]
32. Deletion involving the TWIST locus and the HOXA cluster: a contiguous gene syndrome on 7p?
Kosaki R; Higuchi M; Mitsui N; Matsushima K; Ohashi H; Kosaki K
Congenit Anom (Kyoto); 2005 Mar; 45(1):35-8. PubMed ID: 15737130
[TBL] [Abstract][Full Text] [Related]
33. A diagnostic approach to identifying submicroscopic 7p21 deletions in Saethre-Chotzen syndrome: fluorescence in situ hybridization and dosage-sensitive Southern blot analysis.
Gripp KW; Kasparcova V; McDonald-McGinn DM; Bhatt S; Bartlett SP; Storm AL; Drumheller TC; Emanuel BS; Zackai EH; Stolle CA
Genet Med; 2001; 3(2):102-8. PubMed ID: 11280946
[TBL] [Abstract][Full Text] [Related]
34. Saethre-Chotzen syndrome with familial translocation at chromosome 7p22.
Reid CS; McMorrow LE; McDonald-McGinn DM; Grace KJ; Ramos FJ; Zackai EH; Cohen MM; Jabs EW
Am J Med Genet; 1993 Oct; 47(5):637-9. PubMed ID: 8266989
[TBL] [Abstract][Full Text] [Related]
35. Evidence for locus heterogeneity in acrocephalosyndactyly: a refined localization for the Saethre-Chotzen syndrome locus on distal chromosome 7p--and exclusion of Jackson-Weiss syndrome from craniosynostosis loci on 7p and 5q.
van Herwerden L; Rose CS; Reardon W; Brueton LA; Weissenbach J; Malcolm S; Winter RM
Am J Hum Genet; 1994 Apr; 54(4):669-74. PubMed ID: 8128964
[TBL] [Abstract][Full Text] [Related]
36. Saethre-Chotzen syndrome associated with balanced translocations involving 7p21: three further families.
Wilkie AO; Yang SP; Summers D; Poole MD; Reardon W; Winter RM
J Med Genet; 1995 Mar; 32(3):174-80. PubMed ID: 7783164
[TBL] [Abstract][Full Text] [Related]
37. Mutations of the TWIST gene in the Saethre-Chotzen syndrome.
el Ghouzzi V; Le Merrer M; Perrin-Schmitt F; Lajeunie E; Benit P; Renier D; Bourgeois P; Bolcato-Bellemin AL; Munnich A; Bonaventure J
Nat Genet; 1997 Jan; 15(1):42-6. PubMed ID: 8988167
[TBL] [Abstract][Full Text] [Related]
38. Saethre-Chotzen syndrome: a clinical, EEG and neuroradiological study.
Elia M; Musumeci SA; Ferri R; Greco D; Romano C; Del Gracco S; Stefanini MC
Childs Nerv Syst; 1996 Nov; 12(11):699-704. PubMed ID: 9118134
[TBL] [Abstract][Full Text] [Related]
39. Altered bone growth dynamics prefigure craniosynostosis in a zebrafish model of Saethre-Chotzen syndrome.
Teng CS; Ting MC; Farmer DT; Brockop M; Maxson RE; Crump JG
Elife; 2018 Oct; 7():. PubMed ID: 30375332
[TBL] [Abstract][Full Text] [Related]
40. Saethre-Chotzen syndrome: a broad and variable pattern of skeletal malformations.
Friedman JM; Hanson JW; Graham CB; Smith DW
J Pediatr; 1977 Dec; 91(6):929-23. PubMed ID: 925822
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
