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Journal Abstract Search
183 related items for PubMed ID: 26847959
1. Simpson-Golabi-Behmel syndrome: a prenatal diagnosis in a foetus with GPC3 and GPC4 gene microduplications. Mujezinović F, Krgović D, Blatnik A, Zagradišnik B, Vipotnik TV, Golec T, Tul N, Vokač NK. Clin Genet; 2016 Jul; 90(1):99-101. PubMed ID: 26847959 [No Abstract] [Full Text] [Related]
2. Simpson-Golabi-Behmel syndrome diagnosed by postmortem magnetic resonance imaging, restricted autopsy, and molecular genetics: a case report. Ochiai D, Ohashi H, Hisazumi-Watanabe H, Sato Y, Yakubo K, Fukuiya T. Eur J Obstet Gynecol Reprod Biol; 2013 Dec; 171(2):388-9. PubMed ID: 24169032 [No Abstract] [Full Text] [Related]
3. CUGC for Simpson-Golabi-Behmel syndrome (SGBS). Vuillaume ML, Moizard MP, Baumer A, Cottereau E, Brioude F, Rauch A, Toutain A. Eur J Hum Genet; 2019 Apr; 27(4):663-668. PubMed ID: 30683921 [Abstract] [Full Text] [Related]
4. Whole exome sequencing aids the diagnosis of Simpson-Golabi-Behmel syndrome in two male fetuses. Xiang J, Zhang Q, Song X, Liu Y, Li H, Li H, Wang T. J Int Med Res; 2020 Jan; 48(1):300060519859752. PubMed ID: 31304847 [Abstract] [Full Text] [Related]
5. Simpson-Golabi-Behmel syndrome type 1 and hepatoblastoma in a patient with a novel exon 2-4 duplication of the GPC3 gene. Mateos ME, Beyer K, López-Laso E, Siles JL, Pérez-Navero JL, Peña MJ, Guzmán J, Matas J. Am J Med Genet A; 2013 May; 161A(5):1091-5. PubMed ID: 23463737 [Abstract] [Full Text] [Related]
15. A patient with Simpson-Golabi-Behmel syndrome, biliary cirrhosis and successful liver transplantation. Jedraszak G, Girard M, Mellos A, Djeddi DD, Chardot C, Vanrenterghem A, Moizard MP, Gondry J, Sevestre H, Mathieu-Dramard M, Lacaille F, Demeer B. Am J Med Genet A; 2014 Mar; 164A(3):774-7. PubMed ID: 24357529 [Abstract] [Full Text] [Related]
16. Are all Xq26.2 duplications overlapping GPC3 on array-CGH a cause of Simpson-Golabi-Behmel syndrome? When do we need transcript analysis? Vuillaume ML, Moizard MP, Hammouche E, Delrue MA, Perrin L, Maftei C, Dupont C, Drunat S, Cottereau E, Baumann C, Toutain A. Clin Genet; 2018 May; 93(5):1111-1113. PubMed ID: 29372559 [No Abstract] [Full Text] [Related]