BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

185 related articles for article (PubMed ID: 8209925)

  • 21. A patient with a unique frameshift mutation in GPC3, causing Simpson-Golabi-Behmel syndrome, presenting with craniosynostosis, penoscrotal hypospadias, and a large prostatic utricle.
    Villarreal DD; Villarreal H; Paez AM; Peppas D; Lynch J; Roeder E; Powers GC
    Am J Med Genet A; 2013 Dec; 161A(12):3121-5. PubMed ID: 24115482
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Severe microphthalmia, diaphragmatic hernia and Fallot's tetralogy associated with a chromosome 1;15 translocation.
    Smith SA; Martin KE; Dodd KL; Young ID
    Clin Dysmorphol; 1994 Oct; 3(4):287-91. PubMed ID: 7894732
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Mutational analysis of the GPC3/GPC4 glypican gene cluster on Xq26 in patients with Simpson-Golabi-Behmel syndrome: identification of loss-of-function mutations in the GPC3 gene.
    Veugelers M; Cat BD; Muyldermans SY; Reekmans G; Delande N; Frints S; Legius E; Fryns JP; Schrander-Stumpel C; Weidle B; Magdalena N; David G
    Hum Mol Genet; 2000 May; 9(9):1321-8. PubMed ID: 10814714
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Simpson-Golabi-Behmel syndrome: follow-up of the Michigan family.
    Opitz JM; Herrmann J; Gilbert EF; Matalon R
    Am J Med Genet; 1988; 30(1-2):301-8. PubMed ID: 3177456
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Whole exome sequencing and array-based molecular karyotyping as aids to prenatal diagnosis in fetuses with suspected Simpson-Golabi-Behmel syndrome.
    Kehrer C; Hoischen A; Menkhaus R; Schwab E; Müller A; Kim S; Kreiß M; Weitensteiner V; Hilger A; Berg C; Geipel A; Reutter H; Gembruch U
    Prenat Diagn; 2016 Oct; 36(10):961-965. PubMed ID: 27589329
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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; 52(5):525-8. PubMed ID: 21434539
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Diaphragmatic hernia and Fryns syndrome phenotype in partial trisomy 22.
    de Beaufort C; Schneider F; Chafai R; Colette JM; Delneste D; Pierquin G
    Genet Couns; 2000; 11(2):181-2. PubMed ID: 10893671
    [No Abstract]   [Full Text] [Related]  

  • 29. Nonisolated diaphragmatic hernia in Simpson-Golabi-Behmel syndrome.
    Chong K; Saleh M; Injeyan M; Miron I; Fong K; Shannon P
    Prenat Diagn; 2018 Jan; 38(2):117-122. PubMed ID: 29240237
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Speech and language in Simpson-Golabi-Behmel syndrome: a case report.
    Van Borsel J; Baudonck N; Verhaaren H; Van Lierde K
    Genet Couns; 2008; 19(2):241-9. PubMed ID: 18619000
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Simpson-Golabi-Behmel syndrome types I and II.
    Tenorio J; Arias P; Martínez-Glez V; Santos F; García-Miñaur S; Nevado J; Lapunzina P
    Orphanet J Rare Dis; 2014 Sep; 9():138. PubMed ID: 25238977
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Simpson-Golabi-Behmel syndrome: genotype/phenotype analysis of 18 affected males from 7 unrelated families.
    Hughes-Benzie RM; Pilia G; Xuan JY; Hunter AG; Chen E; Golabi M; Hurst JA; Kobori J; Marymee K; Pagon RA; Punnett HH; Schelley S; Tolmie JL; Wohlferd MM; Grossman T; Schlessinger D; MacKenzie AE
    Am J Med Genet; 1996 Dec; 66(2):227-34. PubMed ID: 8958336
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Hungarian case with Costello syndrome and translocation t(1,22).
    Czeizel AE; Tímár L
    Am J Med Genet; 1995 Jul; 57(3):501-3. PubMed ID: 7677162
    [No Abstract]   [Full Text] [Related]  

  • 35. 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; 44(5):327-9. PubMed ID: 10496077
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Simpson-Golabi-Behmel syndrome and attention deficit hyperactivity disorder in two brothers.
    Savarirayan R; Bankier A
    J Med Genet; 1999 Jul; 36(7):574-6. PubMed ID: 10424824
    [No Abstract]   [Full Text] [Related]  

  • 37. [Cerebral gigantism: report on two familial cases (author's transl)].
    Krauel X; Berger R; Amiel-Tison C
    J Genet Hum; 1977 Oct; 25(3):205-14. PubMed ID: 591926
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [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]  

  • 39. [X chromosome inactivation in 2 cases of X/autosome translocation].
    Balícek P; Jüttnerová V; Zizka J; Olivková E
    Cas Lek Cesk; 1987 Mar; 126(12):374-7. PubMed ID: 3581129
    [No Abstract]   [Full Text] [Related]  

  • 40. The Simpson-Golabi-Behmel syndrome causative glypican-3, binds to and inhibits the dipeptidyl peptidase activity of CD26.
    Davoodi J; Kelly J; Gendron NH; MacKenzie AE
    Proteomics; 2007 Jun; 7(13):2300-10. PubMed ID: 17549790
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.