155 related articles for article (PubMed ID: 3177456)
1. Simpson-Golabi-Behmel syndrome: follow-up of the Michigan family.
Opitz JM; Herrmann J; Gilbert EF; Matalon R
Am J Med Genet; 1988; 30(1-2):301-8. PubMed ID: 3177456
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 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]
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. 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]
7. 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]
8. 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]
9. 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]
10. 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]
11. 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]
12. 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]
13. [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]
14. 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]
15. 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]
16. The Simpson-Golabi-Behmel syndrome: A clinical case and a detective story.
Gurrieri F; Pomponi MG; Pietrobono R; Lucci-Cordisco E; Silvestri E; Storniello G; Neri G
Am J Med Genet A; 2011 Jan; 155A(1):145-8. PubMed ID: 21204223
[TBL] [Abstract][Full Text] [Related]
17. Simpson-Golabi-Behmel syndrome with severe cardiac arrhythmias.
König R; Fuchs S; Kern C; Langenbeck U
Am J Med Genet; 1991; 38(2-3):244-7. PubMed ID: 2018065
[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. 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]
20. A new X-linked dysplasia gigantism syndrome: identical with the Simpson dysplasia syndrome?
Behmel A; Plöchl E; Rosenkranz W
Hum Genet; 1984; 67(4):409-13. PubMed ID: 6490008
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
