136 related articles for article (PubMed ID: 35482990)
1. A prenatal case of Simpson-Golabi-Behmel syndrome type 1 with a 0.26-Mb deletion fragment at Xq26.2 inherited from mother: Case report.
Sha J; Tan F; Liu Y; Xu Z; Wang X; Zhai J
Medicine (Baltimore); 2022 Apr; 101(16):e29222. PubMed ID: 35482990
[TBL] [Abstract][Full Text] [Related]
2. Prenatal diagnosis of Simpson-Golabi-Behmel syndrome type 1 with an 814 kb Xq26.2 deletion with the initial presentation of a thick nuchal fold.
Peng HH; Yu CJ; Chen YC; Hsu CC; Chang SD; Chueh HY; Chang YL; Cheng PJ; Lee YC
Taiwan J Obstet Gynecol; 2023 Jan; 62(1):163-166. PubMed ID: 36720533
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
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. 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]
7. Simpson-Golabi-Behmel syndrome type 1 with subclinical hypothyroidism: A case report.
Zhang J; Mu K; Xu H; Guo Y; Liu Z; Wang L; Li J; Zhang F; Kou Y; Yuan X
Medicine (Baltimore); 2019 Oct; 98(43):e17616. PubMed ID: 31651874
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. 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]
11. 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]
12. Simpson-Golabi-Behmel syndrome type 1 with normal birth parameters.
Chung BHY; Yeow SS; Chan JCK; Lee M
BMJ Case Rep; 2024 Mar; 17(3):. PubMed ID: 38442972
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. 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]
16. 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]
17. Nonisolated diaphragmatic hernia in Simpson-Golabi-Behmel syndrome.
Chong K; Saleh M; Injeyan M; Miron I; Fong K; Shannon P
Prenat Diagn; 2018 Jan; 38(2):117-122. PubMed ID: 29240237
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. A fetus with Bosch-Boonstra-Schaaf optic atrophy syndrome characterized by bilateral ventricle widening: A case report and related literature review.
Sun Y; Guo L; Sha J; Tao H; Wang X; Liu Y; Zhai J; Wu J; Zhao Y
Medicine (Baltimore); 2022 Oct; 101(40):e30558. PubMed ID: 36221391
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
