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3. Report of another family with Simpson-Golabi-Behmel syndrome and a review of the literature. Garganta CL; Bodurtha JN Am J Med Genet; 1992 Sep; 44(2):129-35. PubMed ID: 1456279 [TBL] [Abstract][Full Text] [Related]
4. Further delineation of the Simpson-Golabi-Behmel (SGB) syndrome. Gurrieri F; Cappa M; Neri G Am J Med Genet; 1992 Sep; 44(2):136-7. PubMed ID: 1456280 [TBL] [Abstract][Full Text] [Related]
5. [The Simpson-Golabi-Behmel syndrome. The stages of a diagnostic procedure]. Di Rocco M; Lignana E; Faraci M; Leveratto L; Borrone C Minerva Pediatr; 1993 Apr; 45(4):163-7. PubMed ID: 8355647 [TBL] [Abstract][Full Text] [Related]
6. Infantile lethal variant of Simpson-Golabi-Behmel syndrome associated with hydrops fetalis. Terespolsky D; Farrell SA; Siegel-Bartelt J; Weksberg R Am J Med Genet; 1995 Nov; 59(3):329-33. PubMed ID: 8599356 [TBL] [Abstract][Full Text] [Related]
7. [Simpson-Golabi-Behmel syndrome. A new overgrowth syndrome with increased risk of tumor development]. Weidle B; Orstavik KH Tidsskr Nor Laegeforen; 1998 Apr; 118(10):1556-8. PubMed ID: 9615582 [TBL] [Abstract][Full Text] [Related]
8. [Anesthetic management of a patient with Young-Simpson syndrome]. Manaka S; Yamanaka I; Tateda T; Tajiri O Masui; 2002 Nov; 51(11):1272-4. PubMed ID: 12481459 [TBL] [Abstract][Full Text] [Related]
9. Further delineation of the Simpson-Golabi-Behmel (SGB) syndrome. Lin AE Am J Med Genet; 1993 Jun; 46(5):606-7. PubMed ID: 8322829 [No Abstract] [Full Text] [Related]
11. Gene for Simpson-Golabi-Behmel syndrome is linked to HPRT in Xq26 in two European families. Orth U; Gurrieri F; Behmel A; Genuardi M; Cremer M; Gal A; Neri G Am J Med Genet; 1994 May; 50(4):388-90. PubMed ID: 8209924 [TBL] [Abstract][Full Text] [Related]
12. Simpson-Golabi-Behmel syndrome: an X-linked encephalo-tropho-schisis syndrome. Neri G; Marini R; Cappa M; Borrelli P; Opitz JM Am J Med Genet; 1988; 30(1-2):287-99. PubMed ID: 3177455 [TBL] [Abstract][Full Text] [Related]
13. Weaver syndrome in two Japanese children. Kondo I; Mori Y; Kuwajima K Am J Med Genet; 1991 Nov; 41(2):221-4. PubMed ID: 1785638 [TBL] [Abstract][Full Text] [Related]
14. New airway and swallow manifestations of Simpson-Golabi-Behmel syndrome. Glamuzina E; Aftimos S; Keesing M; Mahadevan M Int J Pediatr Otorhinolaryngol; 2009 Oct; 73(10):1464-6. PubMed ID: 19631996 [TBL] [Abstract][Full Text] [Related]
15. The Golabi-Rosen syndrome--report of a second family. Opitz JM Am J Med Genet; 1984 Jan; 17(1):359-66. PubMed ID: 6538756 [TBL] [Abstract][Full Text] [Related]
16. Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome. Pilia G; Hughes-Benzie RM; MacKenzie A; Baybayan P; Chen EY; Huber R; Neri G; Cao A; Forabosco A; Schlessinger D Nat Genet; 1996 Mar; 12(3):241-7. PubMed ID: 8589713 [TBL] [Abstract][Full Text] [Related]
17. Multiple odontogenic keratocysts in mental retardation-overgrowth (Simpson-Golabi-Behmel) syndrome. Krimmel M; Reinert S Br J Oral Maxillofac Surg; 2000 Jun; 38(3):221-3. PubMed ID: 10864729 [TBL] [Abstract][Full Text] [Related]
18. Simpson Golabi Behmel syndrome: progress toward understanding the molecular basis for overgrowth, malformation, and cancer predisposition. DeBaun MR; Ess J; Saunders S Mol Genet Metab; 2001 Apr; 72(4):279-86. PubMed ID: 11286501 [TBL] [Abstract][Full Text] [Related]
19. Familial Simpson-Golabi-Behmel syndrome: studies of X-chromosome inactivation and clinical phenotypes in two female individuals with GPC3 mutations. Yano S; Baskin B; Bagheri A; Watanabe Y; Moseley K; Nishimura A; Matsumoto N; Ray PN Clin Genet; 2011 Nov; 80(5):466-71. PubMed ID: 20950395 [TBL] [Abstract][Full Text] [Related]
20. Anesthetic considerations of two sisters with Beckwith-Wiedemann syndrome. Kim Y; Shibutani T; Hirota Y; Mahbub SF; Matsuura H Anesth Prog; 1996; 43(1):24-8. PubMed ID: 10323122 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]