BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

164 related articles for article (PubMed ID: 30553040)

  • 1. Synchronous occurrence of multiple distinct jaw lesions in Simpson-Golabi-Behmel Syndrome: A case report.
    Kaya GŞ; Özalp Ö; Özbudak İH
    J Stomatol Oral Maxillofac Surg; 2019 Nov; 120(5):483-488. PubMed ID: 30553040
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Distinctive findings in a boy with Simpson-Golabi-Behmel syndrome.
    Halayem S; Hamza M; Maazoul F; Ben Turkia H; Touati M; Tebib N; Mrad R; Bouden A
    Am J Med Genet A; 2016 Apr; 170A(4):1035-9. PubMed ID: 26692054
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Rare dental manifestation in Simpson-Golabi-Behmel syndrome.
    Parashar P; Preston S; Brada B; Borris T; Potter B
    Gen Dent; 2016; 64(1):e12-5. PubMed ID: 26742178
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Twenty-one years to the right diagnosis - clinical overlap of Simpson-Golabi-Behmel and Beckwith-Wiedemann syndrome.
    Knopp C; Rudnik-Schöneborn S; Zerres K; Gencik M; Spengler S; Eggermann T
    Am J Med Genet A; 2015 Jan; 167A(1):151-5. PubMed ID: 25339544
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Simpson-Golabi-Behmel syndrome associated with cleft palate.
    Morita Y; Kimoto N; Ogawa H; Omata T; Morita N
    J Craniofac Surg; 2011 Sep; 22(5):1917-8. PubMed ID: 21959466
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. Ovotesticular Disorder of Sex Development (Ovotestis) in Simpson-Golabi-Behmel Syndrome: Expansion of the Clinical Spectrum.
    De Paepe ME; Young L; Jones JR; Tantravahi U
    Pediatr Dev Pathol; 2019; 22(1):70-74. PubMed ID: 29652239
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Simpson-Golabi-Behmel syndrome in one of the Dichorionic-diamniotic twin: a case report and literature review.
    Guo Y; Zhang H; Fan L; Chen J; Zhang X; Yang H; Sun Y
    BMC Pregnancy Childbirth; 2022 Jan; 22(1):42. PubMed ID: 35038998
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. Clinical and oral findings of a patient with Simpson-Golabi-Behmel syndrome.
    Bayram M; Yildirim M; Seymen F
    Eur Arch Paediatr Dent; 2015 Feb; 16(1):63-6. PubMed ID: 25245233
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Simpson-Golabi-Behmel syndrome with 46,XY disorders of sex development: A case report.
    Fu Q; Wang H; Qi Z; Zhang Y
    Am J Med Genet A; 2019 Feb; 179(2):285-289. PubMed ID: 30667571
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. Prenatal findings and the genetic diagnosis of fetal overgrowth disorders: Simpson-Golabi-Behmel syndrome, Sotos syndrome, and Beckwith-Wiedemann syndrome.
    Chen CP
    Taiwan J Obstet Gynecol; 2012 Jun; 51(2):186-91. PubMed ID: 22795092
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.