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Journal Abstract Search
145 related items for PubMed ID: 8322829
1. Further delineation of the Simpson-Golabi-Behmel (SGB) syndrome. Lin AE. Am J Med Genet; 1993 Jun 15; 46(5):606-7. PubMed ID: 8322829 [No Abstract] [Full Text] [Related]
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 15; 44(2):129-35. PubMed ID: 1456279 [Abstract] [Full Text] [Related]
4. 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 01; 50(4):388-90. PubMed ID: 8209924 [Abstract] [Full Text] [Related]
5. Simpson-Golabi-Behmel syndrome and attention deficit hyperactivity disorder in two brothers. Savarirayan R, Bankier A. J Med Genet; 1999 Jul 01; 36(7):574-6. PubMed ID: 10424824 [No Abstract] [Full Text] [Related]
6. [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 01; 45(4):163-7. PubMed ID: 8355647 [Abstract] [Full Text] [Related]
7. [Anesthetic management in a patient with Simpson-Golabi-Behmel syndrome]. Tsuchiya K, Takahata O, Sengoku K, Hamada I, Suzuki A, Iwasaki H. Masui; 2001 Oct 01; 50(10):1106-8. PubMed ID: 11712343 [Abstract] [Full Text] [Related]
8. Simpson-Golabi-Behmel syndrome: congenital diaphragmatic hernia and radiologic findings in two patients and follow-up of a previously reported case. Chen E, Johnson JP, Cox VA, Golabi M. Am J Med Genet; 1993 Jun 15; 46(5):574-8. PubMed ID: 8322824 [Abstract] [Full Text] [Related]
9. [Simpson-Golabi-Behmel syndrome. A new overgrowth syndrome with increased risk of tumor development]. Weidle B, Orstavik KH. Tidsskr Nor Laegeforen; 1998 Apr 20; 118(10):1556-8. PubMed ID: 9615582 [Abstract] [Full Text] [Related]
10. Simpson-Golabi-Behmel syndrome (SGBS) in a female with an X-autosome translocation. Punnett HH. Am J Med Genet; 1994 May 01; 50(4):391-3. PubMed ID: 8209925 [No Abstract] [Full Text] [Related]
12. Fryns syndrome without diaphragmatic hernia? Willems PJ, Keersmaekers GH, Dom KE, Colpaert C, Schatteman E, Vergote IB, Dumon JE. Am J Med Genet; 1991 Nov 01; 41(2):255-7. PubMed ID: 1785645 [Abstract] [Full Text] [Related]
13. 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 01; 12(3):241-7. PubMed ID: 8589713 [Abstract] [Full Text] [Related]
14. Borjeson-Forssman-Lehmann syndrome and dilated cardiomyopathy: a previously unreported association. Kaplinsky E, Perandones C, Galiana MG, Fideleff H, Favaloro RR, Carlos V, Perrone SV. Can J Cardiol; 2001 Jan 01; 17(1):80-3. PubMed ID: 11173318 [Abstract] [Full Text] [Related]
15. Brief clinical report: renal hypodysplasia and unilateral ovarian agenesis in the penta-X syndrome. Toussi T, Halal F, Lesage R, Delorme F, Bergeron A. Am J Med Genet; 1980 Jan 01; 6(2):153-62. PubMed ID: 7446561 [Abstract] [Full Text] [Related]
16. 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 Jan 01; 30(1-2):287-99. PubMed ID: 3177455 [Abstract] [Full Text] [Related]
20. Clinical and molecular aspects of the Simpson-Golabi-Behmel syndrome. Neri G, Gurrieri F, Zanni G, Lin A. Am J Med Genet; 1998 Oct 02; 79(4):279-83. PubMed ID: 9781908 [Abstract] [Full Text] [Related] Page: [Next] [New Search]