BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

158 related articles for article (PubMed ID: 36720533)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. Increased nuchal translucency and other ultrasound findings in a case of simpson-golabi-behmel syndrome.
    Li CC; McDonald SD
    Fetal Diagn Ther; 2009; 25(2):211-5. PubMed ID: 19372699
    [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. 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]  

  • 7. 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]  

  • 8. Prenatal diagnosis and array comparative genomic hybridization characterization of trisomy 21 in a fetus associated with right congenital diaphragmatic hernia and a review of the literature of chromosomal abnormalities associated with congenital diaphragmatic hernia.
    Chen CP; Wang YL; Chern SR; Liu YP; Peng CR; Kuo YL; Wu PS; Chen WL; Wang W
    Taiwan J Obstet Gynecol; 2015 Feb; 54(1):66-70. PubMed ID: 25675923
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Fetal nuchal translucency thickness at 10-14 weeks' gestation and congenital diaphragmatic hernia.
    Sebire NJ; Snijders RJ; Davenport M; Greenough A; Nicolaides KH
    Obstet Gynecol; 1997 Dec; 90(6):943-6. PubMed ID: 9397108
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prenatal diagnosis of de novo proximal interstitial deletion of 9q and review of the literature of uncommon aneuploidies associated with increased nuchal translucency.
    Chen CP; Chern SR; Chang TY; Chen WL; Chen LF; Wang W; Cindy Chen HE
    Prenat Diagn; 2005 May; 25(5):383-9. PubMed ID: 15906429
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. Prenatal diagnosis of a fetus with androgen insensitivity syndrome (AIS).
    Yalinkaya A; Yayla M; Erdemoglu M
    Prenat Diagn; 2007 Sep; 27(9):856-7. PubMed ID: 17605153
    [TBL] [Abstract][Full Text] [Related]  

  • 15. First reported case of Simpson-Golabi-Behmel syndrome in a female fetus diagnosed prenatally with chromosomal microarray.
    Støve HK; Becher N; Gjørup V; Ramsing M; Vogel I; Vestergaard EM
    Clin Case Rep; 2017 May; 5(5):608-612. PubMed ID: 28469860
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 5p deletion with congenital diaphragmatic hernia: a case report.
    Kotani T; Ushida T; Nakamura N; Imai K; Iitani Y; Tano S; Iwagaki S; Takahashi Y; Ito M; Hayakawa M; Kajiyama H
    J Med Case Rep; 2022 Oct; 16(1):390. PubMed ID: 36261840
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Perlman syndrome: report, prenatal findings and review.
    Alessandri JL; Cuillier F; Ramful D; Ernould S; Robin S; de Napoli-Cocci S; Rivière JP; Rossignol S
    Am J Med Genet A; 2008 Oct; 146A(19):2532-7. PubMed ID: 18780370
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prenatal diagnosis of Wolf-Hirschhorn syndrome (4p-) in association with congenital diaphragmatic hernia, cystic hygroma and IUGR.
    Basgul A; Kavak ZN; Akman I; Basgul A; Gokaslan H; Elcioglu N
    Clin Exp Obstet Gynecol; 2006; 33(2):105-6. PubMed ID: 16903248
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.