BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

185 related articles for article (PubMed ID: 8209925)

  • 1. Simpson-Golabi-Behmel syndrome (SGBS) in a female with an X-autosome translocation.
    Punnett HH
    Am J Med Genet; 1994 May; 50(4):391-3. PubMed ID: 8209925
    [No Abstract]   [Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. [Simpson-Golabi-Behmel syndrome].
    Kubota T
    Ryoikibetsu Shokogun Shirizu; 2001; (34 Pt 2):638-9. PubMed ID: 11528938
    [No Abstract]   [Full Text] [Related]  

  • 9. 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]  

  • 10. Child with Sotos phenotype and a 5:15 translocation.
    Maroun C; Schmerler S; Hutcheon RG
    Am J Med Genet; 1994 Apr; 50(3):291-3. PubMed ID: 8042674
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Simpson-Golabi-Behmel syndrome in a 39-year-old male patient with suspected acromegaly-A case study.
    Andrysiak-Mamos E; Sagan KP; Lietz-Kijak D; Kijak E; Kaźmierczak B; Pietrzyk A; Sowinska-Przepiera E; Sagan L; Syrenicz A
    Am J Med Genet A; 2019 Feb; 179(2):322-328. PubMed ID: 30592149
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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; 46(5):574-8. PubMed ID: 8322824
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mapping of Simpson-Golabi-Behmel syndrome to Xq25-q27.
    Xuan JY; Besner A; Ireland M; Hughes-Benzie RM; MacKenzie AE
    Hum Mol Genet; 1994 Jan; 3(1):133-7. PubMed ID: 7909248
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. A 1 Mb-sized microdeletion Xq26.2 encompassing the GPC3 gene in a fetus with Simpson-Golabi-Behmel syndrome Report, antenatal findings and review.
    Weichert J; Schröer A; Amari F; Siebert R; Caliebe A; Nagel I; Gillessen-Kaesbach G; Mohrmann I; Hellenbroich Y
    Eur J Med Genet; 2011; 54(3):343-7. PubMed ID: 21362501
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [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; 50(10):1106-8. PubMed ID: 11712343
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Perinatal Case of Fatal Simpson-Golabi-Behmel Syndrome with Hyperplasia of Seminiferous Tubules.
    Zimmermann N; Stanek J
    Am J Case Rep; 2017 Jun; 18():649-655. PubMed ID: 28600484
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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; 36(1):57-8. PubMed ID: 9950367
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [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]  

    [Next]    [New Search]
    of 10.