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7. Molecular analysis of a novel intragenic deletion in GPC3 in three cousins with Simpson-Golabi-Behmel syndrome. Schmidt J, Hollstein R, Kaiser FJ, Gillessen-Kaesbach G. Am J Med Genet A; 2017 May; 173(5):1400-1405. PubMed ID: 28371070 [Abstract] [Full Text] [Related]
9. GPC6, a novel member of the glypican gene family, encodes a product structurally related to GPC4 and is colocalized with GPC5 on human chromosome 13. Paine-Saunders S, Viviano BL, Saunders S. Genomics; 1999 May 01; 57(3):455-8. PubMed ID: 10329016 [Abstract] [Full Text] [Related]
11. Glypican-3-deficient mice exhibit developmental overgrowth and some of the abnormalities typical of Simpson-Golabi-Behmel syndrome. Cano-Gauci DF, Song HH, Yang H, McKerlie C, Choo B, Shi W, Pullano R, Piscione TD, Grisaru S, Soon S, Sedlackova L, Tanswell AK, Mak TW, Yeger H, Lockwood GA, Rosenblum ND, Filmus J. J Cell Biol; 1999 Jul 12; 146(1):255-64. PubMed ID: 10402475 [Abstract] [Full Text] [Related]
12. A small interstitial deletion in the GPC3 gene causes Simpson-Golabi-Behmel syndrome in a Dutch-Canadian family. Xuan JY, Hughes-Benzie RM, MacKenzie AE. J Med Genet; 1999 Jan 12; 36(1):57-8. PubMed ID: 9950367 [Abstract] [Full Text] [Related]
13. A 4-Mb BAC/PAC contig and complete genomic structure of the GPC5/GPC6 gene cluster on chromosome 13q32. Veugelers M, De Cat B, Delande N, Esselens C, Bonk I, Vermeesch J, Marynen P, Fryns JP, David G. Matrix Biol; 2001 Sep 12; 20(5-6):375-85. PubMed ID: 11566272 [Abstract] [Full Text] [Related]
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15. 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 01; 80(5):466-71. PubMed ID: 20950395 [Abstract] [Full Text] [Related]
16. A clinical and molecular study of a patient with Simpson-Golabi-Behmel syndrome. Okamoto N, Yagi M, Imura K, Wada Y. J Hum Genet; 1999 Nov 01; 44(5):327-9. PubMed ID: 10496077 [Abstract] [Full Text] [Related]
17. OCI-5/GPC3, a glypican encoded by a gene that is mutated in the Simpson-Golabi-Behmel overgrowth syndrome, induces apoptosis in a cell line-specific manner. Gonzalez AD, Kaya M, Shi W, Song H, Testa JR, Penn LZ, Filmus J. J Cell Biol; 1998 Jun 15; 141(6):1407-14. PubMed ID: 9628896 [Abstract] [Full Text] [Related]
18. Duplications of GPC3 and GPC4 genes in symptomatic female carriers of Simpson-Golabi-Behmel syndrome type 1. Schirwani S, Novelli A, Digilio MC, Bourn D, Wilson V, Roberts C, Dallapiccola B, Hobson E. Eur J Med Genet; 2019 Apr 15; 62(4):243-247. PubMed ID: 30048822 [Abstract] [Full Text] [Related]
19. Overgrowth syndromes and genomic imprinting: from mouse to man. Li M, Squire JA, Weksberg R. Clin Genet; 1998 Mar 15; 53(3):165-70. PubMed ID: 9630066 [Abstract] [Full Text] [Related]
20. Novel nonsense mutation of GPC3 gene in a patient with Simpson-Golabi-Behmel syndrome. Ratbi I, Elalaoui SC, Moizard MP, Raynaud M, Sefiani A. Turk J Pediatr; 2010 Mar 15; 52(5):525-8. PubMed ID: 21434539 [Abstract] [Full Text] [Related] Page: [Next] [New Search]