191 related articles for article (PubMed ID: 19631996)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. 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]
8. 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]
9. 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]
10. 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]
11. 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]
12. 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]
13. 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]
14. [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]
15. 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]
16. Simpson-Golabi-Behmel syndrome diagnosed by postmortem magnetic resonance imaging, restricted autopsy, and molecular genetics: a case report.
Ochiai D; Ohashi H; Hisazumi-Watanabe H; Sato Y; Yakubo K; Fukuiya T
Eur J Obstet Gynecol Reprod Biol; 2013 Dec; 171(2):388-9. PubMed ID: 24169032
[No Abstract] [Full Text] [Related]
17. 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]
18. 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]
19. 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]
20. 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]
[Next] [New Search]
