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2. [The Saethre-Chotzen syndrome. Clinical case]. Galluzzi F; Salti R; Marianelli L; La Cauza C Minerva Pediatr; 1980 Mar; 32(5):325-8. PubMed ID: 6104281 [No Abstract] [Full Text] [Related]
3. Saethre-Chotzen syndrome and hyper IgE syndrome in a patient with a novel 11 bp deletion of the TWIST gene. Boeck A; Kosan C; Ciznar P; Kunz J Am J Med Genet; 2001 Nov; 104(1):53-6. PubMed ID: 11746028 [TBL] [Abstract][Full Text] [Related]
4. Cytogenetic evidence that the Saethre-Chotzen gene maps to 7p21.2. Reardon W; McManus SP; Summers D; Winter RM Am J Med Genet; 1993 Oct; 47(5):633-6. PubMed ID: 8266988 [TBL] [Abstract][Full Text] [Related]
5. Saethre-Chotzen syndrome with trigonocephaly. Cristofori G; Filippi G Am J Med Genet; 1992 Nov; 44(5):611-4. PubMed ID: 1481819 [TBL] [Abstract][Full Text] [Related]
6. Genetic analysis of patients with the Saethre-Chotzen phenotype. Chun K; Teebi AS; Jung JH; Kennedy S; Laframboise R; Meschino WS; Nakabayashi K; Scherer SW; Ray PN; Teshima I Am J Med Genet; 2002 Jun; 110(2):136-43. PubMed ID: 12116251 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. Saethre-Chotzen syndrome presenting with incomplete renal Fanconi syndrome. Oktenli C; Saglam M; Zafer E; Gül D Nephron; 2002 Oct; 92(2):463-5. PubMed ID: 12218332 [TBL] [Abstract][Full Text] [Related]
10. Neutrophil chemotaxis in children with recurrent otitis media. Ichimura K Int J Pediatr Otorhinolaryngol; 1982 Mar; 4(1):47-55. PubMed ID: 7095992 [TBL] [Abstract][Full Text] [Related]
11. Women with Saethre-Chotzen syndrome are at increased risk of breast cancer. Sahlin P; Windh P; Lauritzen C; Emanuelsson M; Grönberg H; Stenman G Genes Chromosomes Cancer; 2007 Jul; 46(7):656-60. PubMed ID: 17437280 [TBL] [Abstract][Full Text] [Related]
12. Defective neutrophil motility and recurrent infection. In vitro and in vivo effects of levamisole. Rabson AR; Anderson R; Glover A Clin Exp Immunol; 1978 Jul; 33(1):142-9. PubMed ID: 709909 [TBL] [Abstract][Full Text] [Related]
13. A defect in neutrophil motility in two siblings with recurrent infections and a remarkable family history. Sacchi FT; Ferrari FA; Fortunato A; Maggiore G; Marconi M; Pagani A; Siccardi AG Infection; 1979; 7(1):45-7. PubMed ID: 422255 [TBL] [Abstract][Full Text] [Related]
14. [Granulocytic function in children with selective IGA deficiency and recurrent infections: demonstration of altered chemotaxis]. De Martino M; Vierucci A; Redi Orienti M; Novembre E Boll Ist Sieroter Milan; 1981 May; 60(2):155-62. PubMed ID: 7306391 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. The concurrence of Saethre-Chotzen syndrome and malignancy in a family with in vitro immune dysfunction. McKeen EA; Mulvihill JJ; Levine PH; Dean JH; Howley PM Cancer; 1984 Dec; 54(12):2946-51. PubMed ID: 6093987 [TBL] [Abstract][Full Text] [Related]
17. Dental findings in Saethre-Chotzen syndrome (acrocephalosyndactyly type III): report of case. Goho C ASDC J Dent Child; 1998; 65(2):136-7. PubMed ID: 9617456 [TBL] [Abstract][Full Text] [Related]
18. [Corrective craniofacial surgery in the acrocephalosyndactylia syndrome (Saethre-Chotzen syndrome)]. Eber SW; Luhr HG; Spoerri O; Weigel W; Westmeier M Z Kinderchir; 1986 Oct; 41(5):263-6. PubMed ID: 3788292 [TBL] [Abstract][Full Text] [Related]
19. 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]