These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
209 related articles for article (PubMed ID: 25339544)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. 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]
8. 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]
9. 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]
10. 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]
11. 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]
12. 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]
13. 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]
14. Clinical overlap of Beckwith-Wiedemann, Perlman and Simpson-Golabi-Behmel syndromes: a diagnostic pitfall. Verloes A; Massart B; Dehalleux I; Langhendries JP; Koulischer L Clin Genet; 1995 May; 47(5):257-62. PubMed ID: 7554352 [TBL] [Abstract][Full Text] [Related]
15. Prenatal diagnosis of Simpson-Golabi-Behmel syndrome. Magini P; Palombo F; Boito S; Lanzoni G; Mongelli P; Rizzuti T; Baccarin M; Pippucci T; Seri M; Lalatta F Am J Med Genet A; 2016 Dec; 170(12):3258-3264. PubMed ID: 27612164 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. 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 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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] [Next] [New Search]