BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

150 related articles for article (PubMed ID: 37427042)

  • 1. A Case of Simpson-Golabi-Behmel Syndrome Presenting with Cutaneous Findings.
    Mullins T; Russell A; Johnston C
    HCA Healthc J Med; 2020; 1(6):481-483. PubMed ID: 37427042
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mutation update for the GPC3 gene involved in Simpson-Golabi-Behmel syndrome and review of the literature.
    Vuillaume ML; Moizard MP; Rossignol S; Cottereau E; Vonwill S; Alessandri JL; Busa T; Colin E; Gérard M; Giuliano F; Lambert L; Lefevre M; Kotecha U; Nampoothiri S; Netchine I; Raynaud M; Brioude F; Toutain A
    Hum Mutat; 2018 Jun; 39(6):790-805. PubMed ID: 29637653
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Novel
    Bu W; Zhu M; Li S; Liu H; Liu X
    Balkan J Med Genet; 2021 Nov; 24(2):95-98. PubMed ID: 36249515
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Somatic CTNNB1 mutation in hepatoblastoma from a patient with Simpson-Golabi-Behmel syndrome and germline GPC3 mutation.
    Kosaki R; Takenouchi T; Takeda N; Kagami M; Nakabayashi K; Hata K; Kosaki K
    Am J Med Genet A; 2014 Apr; 164A(4):993-7. PubMed ID: 24459012
    [TBL] [Abstract][Full Text] [Related]  

  • 5. SIMPSON-GOLABI-BEHMEL syndrome type 1: How placental immunohistochemistry can rapidly Predict the diagnosis.
    Fiandrino G; Arossa A; Ghirardello S; Kalantari S; Rossi C; Bonasoni MP; Cesari S; Rizzuti T; Giorgio E; Bassanese F; Scatigno AL; Meroni A; Melito C; Feltri M; Longo S; Figar TA; Andorno A; Gelli MC; Bertozzi M; Spinillo A; Riccipetitoni G; Valente EM; Paulli M; Sirchia F
    Placenta; 2022 Aug; 126():119-124. PubMed ID: 35796063
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Simpson-Golabi-Behmel syndrome in a female: A case report and an unsolved issue.
    Vaisfeld A; Pomponi MG; Pietrobono R; Tabolacci E; Neri G
    Am J Med Genet A; 2017 Jan; 173(1):285-288. PubMed ID: 27739211
    [TBL] [Abstract][Full Text] [Related]  

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

  • 8. 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; 62(4):243-247. PubMed ID: 30048822
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Simpson-Golabi-Behmel syndrome.
    Vaisfeld A; Neri G
    Am J Med Genet C Semin Med Genet; 2024 May; ():e32088. PubMed ID: 38766979
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Simpson-Golabi-Behmel syndrome: One family, same mutation, different outcome.
    Fernandes C; Paúl A; Venâncio MM; Ramos F
    Am J Med Genet A; 2021 Aug; 185(8):2502-2506. PubMed ID: 34003580
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A male newborn with Simpson-Golabi-Behmel syndrome, presenting with metopic synostosis, anal atresia, and total anomalous pulmonary venous return.
    Demir N; Peker E; Ece I; Kaba S; Doğan M; Tuncer O
    Genet Couns; 2014; 25(4):439-43. PubMed ID: 25804025
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. For Debate: The Significance of Etiologic Diagnosis in Neonates with Overgrowth Syndromes. Lesson Learned from the Simpson-Golabi-Behmel Syndrome.
    Plachý L; Elblová L; Neuman V; Fencl F; Bláhová K; Straňák Z; Lebl J; Průhová Š
    Pediatr Endocrinol Rev; 2018 Sep; 16(1):171-177. PubMed ID: 30371035
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prenatal case of Simpson-Golabi-Behmel syndrome with a de novo 370Kb-sized microdeletion of Xq26.2 compassing partial GPC3 gene and review.
    Liu J; Liu Q; Yang S; Ma N; Pang J; Peng Y; Xi H; Jia Z; Luo Y; Jiang M; Teng Y; Yu W; Li Z; Wang H
    Mol Genet Genomic Med; 2021 Aug; 9(8):e1750. PubMed ID: 34293831
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Simpson-Golabi-Behmel syndrome: an X-linked encephalo-tropho-schisis syndrome. 1988.
    Neri G; Marini R; Cappa M; Borrelli P; Opitz JM
    Am J Med Genet A; 2013 Nov; 161A(11):2697-703. PubMed ID: 24166811
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Phenotypic spectrum of Simpson-Golabi-Behmel syndrome in a series of 42 cases with a mutation in GPC3 and review of the literature.
    Cottereau E; Mortemousque I; Moizard MP; Bürglen L; Lacombe D; Gilbert-Dussardier B; Sigaudy S; Boute O; David A; Faivre L; Amiel J; Robertson R; Viana Ramos F; Bieth E; Odent S; Demeer B; Mathieu M; Gaillard D; Van Maldergem L; Baujat G; Maystadt I; Héron D; Verloes A; Philip N; Cormier-Daire V; Frouté MF; Pinson L; Blanchet P; Sarda P; Willems M; Jacquinet A; Ratbi I; Van Den Ende J; Lackmy-Port Lis M; Goldenberg A; Bonneau D; Rossignol S; Toutain A
    Am J Med Genet C Semin Med Genet; 2013 May; 163C(2):92-105. PubMed ID: 23606591
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. GPC3 mutation analysis in a spectrum of patients with overgrowth expands the phenotype of Simpson-Golabi-Behmel syndrome.
    Li M; Shuman C; Fei YL; Cutiongco E; Bender HA; Stevens C; Wilkins-Haug L; Day-Salvatore D; Yong SL; Geraghty MT; Squire J; Weksberg R
    Am J Med Genet; 2001 Aug; 102(2):161-8. PubMed ID: 11477610
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.