BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

165 related articles for article (PubMed ID: 33292381)

  • 21. Prenatal diagnosis of complex phenotype in a 13-week-old fetus with an interstitial multigene deletion 20q13.13.-q13.2 by chromosomal microarray.
    Stipoljev F; Miric-Tesanic D; Hafner T; Barbalic M; Logara M; Lasan-Trcic R; Vicic A; Gjergja-Juraski R
    Eur J Med Genet; 2017 Nov; 60(11):589-594. PubMed ID: 28807863
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 1p36 deletion syndrome associated with Prader-Willi-like phenotype.
    Tsuyusaki Y; Yoshihashi H; Furuya N; Adachi M; Osaka H; Yamamoto K; Kurosawa K
    Pediatr Int; 2010 Aug; 52(4):547-50. PubMed ID: 20113418
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Implication of Genetic Testing and Pregnancy Outcome in a Woman with Unbalanced Translocation t(1;6).
    Jurčenko M; Auzenbaha M; Mičule I; Grīnfelde I; Dzalbs A; Mālniece I
    Am J Case Rep; 2022 Feb; 23():e935370. PubMed ID: 35192596
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Prenatal diagnosis and molecular cytogenetic characterization of chromosome 22q11.2 deletion syndrome associated with congenital heart defects.
    Kuo YL; Chen CP; Wang LK; Ko TM; Chang TY; Chern SR; Wu PS; Chen YT; Chang SY
    Taiwan J Obstet Gynecol; 2014 Jun; 53(2):248-51. PubMed ID: 25017279
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Monosomy1p36.3 and trisomy 19p13.3 in a child with periventricular nodular heterotopia.
    Descartes M; Mikhail FM; Franklin JC; McGrath TM; Bebin M
    Pediatr Neurol; 2011 Oct; 45(4):274-8. PubMed ID: 21907895
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Complex nature of apparently balanced chromosomal rearrangements in patients with autism spectrum disorder.
    Tabet AC; Verloes A; Pilorge M; Delaby E; Delorme R; Nygren G; Devillard F; Gérard M; Passemard S; Héron D; Siffroi JP; Jacquette A; Delahaye A; Perrin L; Dupont C; Aboura A; Bitoun P; Coleman M; Leboyer M; Gillberg C; Benzacken B; Betancur C
    Mol Autism; 2015; 6():19. PubMed ID: 25844147
    [TBL] [Abstract][Full Text] [Related]  

  • 27. OEIS complex associated with chromosome 1p36 deletion: a case report and review.
    El-Hattab AW; Skorupski JC; Hsieh MH; Breman AM; Patel A; Cheung SW; Craigen WJ
    Am J Med Genet A; 2010 Feb; 152A(2):504-11. PubMed ID: 20101692
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Prenatal diagnosis of 1p36.3 microdeletion in a fetus with complex heart defect].
    Wu J; He Z; Lin S; Xie Y; Chen B; Chen J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Jun; 33(3):353-6. PubMed ID: 27264820
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 576 kb deletion in 1p36.33-p36.32 containing SKI is associated with limb malformation, congenital heart disease and epilepsy.
    Zhu X; Zhang Y; Wang J; Yang JF; Yang YF; Tan ZP
    Gene; 2013 Oct; 528(2):352-5. PubMed ID: 23892090
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Abdominal paraganglioma in a young woman with 1p36 deletion syndrome.
    Murakoshi M; Takasawa K; Nishioka M; Asakawa M; Kashimada K; Yoshimoto T; Yamamoto T; Takekoshi K; Ogawa Y; Shimohira M
    Am J Med Genet A; 2017 Feb; 173(2):495-500. PubMed ID: 27774766
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Subtelomeric rearrangements and 22q11.2 deletion syndrome in anomalous growth-restricted fetuses with normal or balanced G-banded karyotype.
    Chen M; Hwu WL; Kuo SJ; Chen CP; Yin PL; Chang SP; Lee DJ; Chen TH; Wang BT; Lin CC
    Ultrasound Obstet Gynecol; 2006 Dec; 28(7):939-43. PubMed ID: 17121426
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Microarray analysis of 50 patients reveals the critical chromosomal regions responsible for 1p36 deletion syndrome-related complications.
    Shimada S; Shimojima K; Okamoto N; Sangu N; Hirasawa K; Matsuo M; Ikeuchi M; Shimakawa S; Shimizu K; Mizuno S; Kubota M; Adachi M; Saito Y; Tomiwa K; Haginoya K; Numabe H; Kako Y; Hayashi A; Sakamoto H; Hiraki Y; Minami K; Takemoto K; Watanabe K; Miura K; Chiyonobu T; Kumada T; Imai K; Maegaki Y; Nagata S; Kosaki K; Izumi T; Nagai T; Yamamoto T
    Brain Dev; 2015 May; 37(5):515-26. PubMed ID: 25172301
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Mild craniosynostosis with 1p36.3 trisomy and 1p36.3 deletion syndrome caused by familial translocation t(Y;1).
    Hiraki Y; Fujita H; Yamamori S; Ohashi H; Eguchi M; Harada N; Mizuguchi T; Matsumoto N
    Am J Med Genet A; 2006 Aug; 140(16):1773-7. PubMed ID: 16835918
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Monosomy 1p36 - a multifaceted and still enigmatic syndrome: four clinically diverse cases with shared white matter abnormalities.
    Õiglane-Shlik E; Puusepp S; Talvik I; Vaher U; Rein R; Tammur P; Reimand T; Teek R; Žilina O; Tomberg T; Õunap K
    Eur J Paediatr Neurol; 2014 May; 18(3):338-46. PubMed ID: 24529875
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Prenatal diagnosis of Smith-Magenis syndrome in two fetuses with increased nuchal translucency, mild lateral ventriculomegaly, and congenital heart defects.
    Lei TY; Li R; Fu F; Wan JH; Zhang YL; Jing XY; Liao C
    Taiwan J Obstet Gynecol; 2016 Dec; 55(6):886-890. PubMed ID: 28040141
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Choroid plexus hyperplasia and monosomy 1p36: report of new findings.
    Puvabanditsin S; Garrow E; Patel N; D'Elia A; Zaafran A; Phattraprayoon N; Davis SE
    J Child Neurol; 2008 Aug; 23(8):922-5. PubMed ID: 18660475
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Electroclinical features of epilepsy associated with 1p36 deletion syndrome: A review.
    Greco M; Ferrara P; Farello G; Striano P; Verrotti A
    Epilepsy Res; 2018 Jan; 139():92-101. PubMed ID: 29212048
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Further delineation of novel 1p36 rearrangements by array-CGH analysis: narrowing the breakpoints and clarifying the "extended" phenotype.
    Giannikou K; Fryssira H; Oikonomakis V; Syrmou A; Kosma K; Tzetis M; Kitsiou-Tzeli S; Kanavakis E
    Gene; 2012 Sep; 506(2):360-8. PubMed ID: 22766398
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Maternal balanced translocation leading to partial duplication of 4q and partial deletion of 1p in a son: cytogenetic and FISH studies using band-specific painting probes generated by chromosome microdissection.
    Chen Z; Grebe TA; Guan XY; Notohamiprodjo M; Nutting PJ; Stone JF; Trent JM; Sandberg AA
    Am J Med Genet; 1997 Aug; 71(2):160-6. PubMed ID: 9217215
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Molecular characterization of a monosomy 1p36 presenting as an Aicardi syndrome phenocopy.
    Bursztejn AC; Bronner M; Peudenier S; Grégoire MJ; Jonveaux P; Nemos C
    Am J Med Genet A; 2009 Nov; 149A(11):2493-500. PubMed ID: 19842196
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.