216 related articles for article (PubMed ID: 8723106)
21. 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]
22. 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]
23. Mutations in TWIST, a basic helix-loop-helix transcription factor, in Saethre-Chotzen syndrome.
Howard TD; Paznekas WA; Green ED; Chiang LC; Ma N; Ortiz de Luna RI; Garcia Delgado C; Gonzalez-Ramos M; Kline AD; Jabs EW
Nat Genet; 1997 Jan; 15(1):36-41. PubMed ID: 8988166
[TBL] [Abstract][Full Text] [Related]
24. Y-craniosynostosis by premature fusion of the metopic and coronal sutures: a new nosological entity or a variety of Saethre-Chotzen syndrome?
di Rocco F; Benoit A; Vigneron J; Segura PB; Klein O; Collet C; Arnaud E
Birth Defects Res A Clin Mol Teratol; 2015 Apr; 103(4):306-10. PubMed ID: 25808521
[TBL] [Abstract][Full Text] [Related]
25. Saethre-Chotzen syndrome: a case report.
Peña WA; Slavotinek A; Oberoi S
Cleft Palate Craniofac J; 2010 May; 47(3):318-21. PubMed ID: 19860490
[TBL] [Abstract][Full Text] [Related]
26. 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]
27. 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]
28. 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]
29. 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]
30. Phenotypic expression of the fibroblast growth factor receptor 3 (FGFR3) mutation P250R in a large craniosynostosis family.
Golla A; Lichmer P; von Gernet S; Winterpacht A; Fairley J; Murken J; Schuffenhauer S
J Med Genet; 1997 Aug; 34(8):683-4. PubMed ID: 9279764
[TBL] [Abstract][Full Text] [Related]
31. Additional phenotypic features of Muenke syndrome in 2 Dutch families.
de Jong T; Mathijssen IM; Hoogeboom AJ
J Craniofac Surg; 2011 Mar; 22(2):571-5. PubMed ID: 21403557
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. Craniosynostosis in Twist heterozygous mice: a model for Saethre-Chotzen syndrome.
Carver EA; Oram KF; Gridley T
Anat Rec; 2002 Oct; 268(2):90-2. PubMed ID: 12221714
[TBL] [Abstract][Full Text] [Related]
34. The breakpoint on 7p in a patient with t(6;7) and craniosynostosis is spanned by a YAC clone containing the D7S503 locus.
Tsuji K; Narahara K; Yokoyama Y; Grzeschik KH; Kunz J
Hum Genet; 1995 Mar; 95(3):303-7. PubMed ID: 7868123
[TBL] [Abstract][Full Text] [Related]
35. [Asymmetric craniofacial stenosis with syndactyly : Saethre-Chotzen syndrome? (author's transl)].
Pellerin P; Walbaum R; Dhellemmes P; Dubois O; Donazzan M
Rev Stomatol Chir Maxillofac; 1981; 82(4):247-50. PubMed ID: 6269174
[No Abstract] [Full Text] [Related]
36. Cephalic malformations in Saethre-Chotzen syndrome. Acrocephalosyndactyly type III.
Evans CA; Christiansen RL
Radiology; 1976 Nov; 121(2):399-403. PubMed ID: 981618
[TBL] [Abstract][Full Text] [Related]
37. Clinical findings in four Brazilian families affected by Saethre-Chotzen syndrome without TWIST mutations.
Nascimento SR; de Mello MP; Batista JC; Balarin MA; Lopes VL
Cleft Palate Craniofac J; 2004 May; 41(3):250-5. PubMed ID: 15151448
[TBL] [Abstract][Full Text] [Related]
38. Familial Saethre-Chotzen syndrome with or without polydactyly of the toe.
Shidayama R; Hirano A; Iio Y; Fujii T
Ann Plast Surg; 1995 Apr; 34(4):435-40. PubMed ID: 7793794
[TBL] [Abstract][Full Text] [Related]
39. Perspectives on craniofacial asymmetry. V. The craniosynostoses.
Cohen MM
Int J Oral Maxillofac Surg; 1995 Jun; 24(3):191-4. PubMed ID: 7594749
[TBL] [Abstract][Full Text] [Related]
40. The TWIST gene, although not disrupted in Saethre-Chotzen patients with apparently balanced translocations of 7p21, is mutated in familial and sporadic cases.
Rose CS; Patel P; Reardon W; Malcolm S; Winter RM
Hum Mol Genet; 1997 Aug; 6(8):1369-73. PubMed ID: 9259286
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
