BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

147 related articles for article (PubMed ID: 29205322)

  • 21. 'Turkish turban' sign: rare phenotype of acrania-exencephaly-anencephaly sequence.
    Tonni G; Grisolia G; Rizzo G; Ruano R; Sepulveda W
    Ultrasound Obstet Gynecol; 2023 Mar; 61(3):417-418. PubMed ID: 36178772
    [No Abstract]   [Full Text] [Related]  

  • 22. Lethal Neural Tube Defects: Reports of Anencephaly and Craniorachischisis Cases and Literature Review.
    Lema AS; Suleyman JS
    Case Rep Obstet Gynecol; 2023; 2023():4017625. PubMed ID: 38148996
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Re: 'Turkish turban' sign: a rare phenotype of acrania-exencephaly-anencephaly sequence.
    Demir N; Yazıcıoglu HF; Mendilcioglu I
    Ultrasound Obstet Gynecol; 2023 Jul; 62(1):158. PubMed ID: 37391929
    [No Abstract]   [Full Text] [Related]  

  • 24. Acalvaria: a case report of a rare congenital malformation and a review of the literature.
    Elveren M; Inci DB; Genco M
    Childs Nerv Syst; 2024 Apr; 40(4):1315-1318. PubMed ID: 38151547
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Neural tube defects: Sex ratio changes after fortification with folic acid.
    Poletta FA; Rittler M; Saleme C; Campaña H; Gili JA; Pawluk MS; Gimenez LG; Cosentino VR; Castilla EE; López-Camelo JS
    PLoS One; 2018; 13(3):e0193127. PubMed ID: 29538416
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Somatic Activating KRAS Mutations in Arteriovenous Malformations of the Brain.
    Nikolaev SI; Vetiska S; Bonilla X; Boudreau E; Jauhiainen S; Rezai Jahromi B; Khyzha N; DiStefano PV; Suutarinen S; Kiehl TR; Mendes Pereira V; Herman AM; Krings T; Andrade-Barazarte H; Tung T; Valiante T; Zadeh G; Tymianski M; Rauramaa T; Ylä-Herttuala S; Wythe JD; Antonarakis SE; Frösen J; Fish JE; Radovanovic I
    N Engl J Med; 2018 Jan; 378(3):250-261. PubMed ID: 29298116
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Digenic variants of planar cell polarity genes in human neural tube defect patients.
    Wang L; Xiao Y; Tian T; Jin L; Lei Y; Finnell RH; Ren A
    Mol Genet Metab; 2018 May; 124(1):94-100. PubMed ID: 29573971
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Vangl2 disruption alters the biomechanics of late spinal neurulation leading to spina bifida in mouse embryos.
    Galea GL; Nychyk O; Mole MA; Moulding D; Savery D; Nikolopoulou E; Henderson DJ; Greene NDE; Copp AJ
    Dis Model Mech; 2018 Mar; 11(3):. PubMed ID: 29590636
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Paternal lineage early onset hereditary ovarian cancers: A Familial Ovarian Cancer Registry study.
    Eng KH; Szender JB; Etter JL; Kaur J; Poblete S; Huang RY; Zhu Q; Grzesik KA; Battaglia S; Cannioto R; Krolewski JJ; Zsiros E; Frederick PJ; Lele SB; Moysich KB; Odunsi KO
    PLoS Genet; 2018 Feb; 14(2):e1007194. PubMed ID: 29447163
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Dysregulation of cotranscriptional alternative splicing underlies CHARGE syndrome.
    Bélanger C; Bérubé-Simard FA; Leduc E; Bernas G; Campeau PM; Lalani SR; Martin DM; Bielas S; Moccia A; Srivastava A; Silversides DW; Pilon N
    Proc Natl Acad Sci U S A; 2018 Jan; 115(4):E620-E629. PubMed ID: 29311329
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Overview on neural tube defects: From development to physical characteristics.
    Avagliano L; Massa V; George TM; Qureshy S; Bulfamante GP; Finnell RH
    Birth Defects Res; 2019 Nov; 111(19):1455-1467. PubMed ID: 30421543
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Genome-wide investigation identifies a rare copy-number variant burden associated with human spina bifida.
    Wolujewicz P; Aguiar-Pulido V; AbdelAleem A; Nair V; Thareja G; Suhre K; Shaw GM; Finnell RH; Elemento O; Ross ME
    Genet Med; 2021 Jul; 23(7):1211-1218. PubMed ID: 33686259
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial model.
    Guo H; Wang T; Wu H; Long M; Coe BP; Li H; Xun G; Ou J; Chen B; Duan G; Bai T; Zhao N; Shen Y; Li Y; Wang Y; Zhang Y; Baker C; Liu Y; Pang N; Huang L; Han L; Jia X; Liu C; Ni H; Yang X; Xia L; Chen J; Shen L; Li Y; Zhao R; Zhao W; Peng J; Pan Q; Long Z; Su W; Tan J; Du X; Ke X; Yao M; Hu Z; Zou X; Zhao J; Bernier RA; Eichler EE; Xia K
    Mol Autism; 2018; 9():64. PubMed ID: 30564305
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Genetic analysis of Wnt/PCP genes in neural tube defects.
    Chen Z; Lei Y; Cao X; Zheng Y; Wang F; Bao Y; Peng R; Finnell RH; Zhang T; Wang H
    BMC Med Genomics; 2018 Apr; 11(1):38. PubMed ID: 29618362
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Identification and functional analysis of rare HECTD1 missense variants in human neural tube defects.
    Oxman E; Li H; Wang HY; Zohn IE
    Hum Genet; 2024 Mar; 143(3):263-277. PubMed ID: 38451291
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Identification and Functional Analysis of Rare HECTD1 Missense Variants in Human Neural Tube Defects.
    Oxman E; Li H; Wang HY; Zohn I
    Res Sq; 2024 Jan; ():. PubMed ID: 38260607
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A quest for genetic causes underlying signaling pathways associated with neural tube defects.
    Rai S; Leydier L; Sharma S; Katwala J; Sahu A
    Front Pediatr; 2023; 11():1126209. PubMed ID: 37284286
    [TBL] [Abstract][Full Text] [Related]  

  • 38.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 39.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 40.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.