BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

280 related articles for article (PubMed ID: 30638470)

  • 1. Phenotype to genotype characterization by array-comparative genomic hydridization (a-CGH) in case of fetal malformations: A systematic review.
    Tonni G; Palmisano M; Perez Zamarian AC; Rabachini Caetano AC; Santana EFM; Peixoto AB; Armbruster-Moraes E; Ruano R; Araujo Júnior E
    Taiwan J Obstet Gynecol; 2019 Jan; 58(1):15-28. PubMed ID: 30638470
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Prenatal Diagnosis by Array Comparative Genomic Hybridization in Fetuses with Cardiac Abnormalities.
    Kowalczyk K; Bartnik-Głaska M; Smyk M; Plaskota I; Bernaciak J; Kędzior M; Wiśniowiecka-Kowalnik B; Jakubów-Durska K; Braun-Walicka N; Barczyk A; Geremek M; Castañeda J; Kutkowska-Kaźmierczak A; Własienko P; Dębska M; Kucińska-Chahwan A; Roszkowski T; Kozłowski S; Mikulska B; Issat T; Obersztyn E; Nowakowska BA
    Genes (Basel); 2021 Dec; 12(12):. PubMed ID: 34946970
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Array comparative genomic hybridization and fetal congenital heart defects: a systematic review and meta-analysis.
    Jansen FA; Blumenfeld YJ; Fisher A; Cobben JM; Odibo AO; Borrell A; Haak MC
    Ultrasound Obstet Gynecol; 2015 Jan; 45(1):27-35. PubMed ID: 25319878
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prenatally diagnosed de novo segmental amplification or deletion by microarray-based comparative genomic hybridization: A retrospective study.
    Peng HH; Lee CH; Su SY; Chen KJ; Lee YC; You SH; Lee WF; Cheng PJ
    Taiwan J Obstet Gynecol; 2019 Sep; 58(5):662-666. PubMed ID: 31542089
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Applied research of combined G-banding and array-CGH in the prenatal diagnosis of ultrasonographic abnormalities in fetuses].
    Fu W; Lu J; Xu L; Zheng L; Zhang Y; Zhong Y; Wang Y; Jin Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Dec; 31(6):737-42. PubMed ID: 25449078
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Detection of submicroscopic chromosomal aberrations by array-based comparative genomic hybridization in fetuses with congenital heart disease.
    Yan Y; Wu Q; Zhang L; Wang X; Dan S; Deng D; Sun L; Yao L; Ma Y; Wang L
    Ultrasound Obstet Gynecol; 2014 Apr; 43(4):404-12. PubMed ID: 24323407
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis: a systematic review and meta-analysis.
    Hillman SC; Pretlove S; Coomarasamy A; McMullan DJ; Davison EV; Maher ER; Kilby MD
    Ultrasound Obstet Gynecol; 2011 Jan; 37(1):6-14. PubMed ID: 20658510
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical utility of array comparative genomic hybridisation for prenatal diagnosis: a cohort study of 3171 pregnancies.
    Lee CN; Lin SY; Lin CH; Shih JC; Lin TH; Su YN
    BJOG; 2012 Apr; 119(5):614-25. PubMed ID: 22313859
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Identification of De Novo and Rare Inherited Copy Number Variants in Children with Syndromic Congenital Heart Defects.
    Hussein IR; Bader RS; Chaudhary AG; Bassiouni R; Alquaiti M; Ashgan F; Schulten HJ; Al Qahtani MH
    Pediatr Cardiol; 2018 Jun; 39(5):924-940. PubMed ID: 29541814
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prenatal diagnosis of proximal partial trisomy 1q confirmed by comparative genomic hybridization array: molecular cytogenetic analysis, fetal pathology and review of the literature.
    Sifakis S; Eleftheriades M; Kappou D; Murru R; Konstantinidou A; Orru S; Ziegler M; Liehr T; Manolakos E; Papoulidis I
    Birth Defects Res A Clin Mol Teratol; 2014 Apr; 100(4):284-93. PubMed ID: 24677675
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Application of single nucleotide polymorphism array in prenatal diagnosis for fetuses with abnormal ultrasound findings].
    Guo YL; Wang L; Xue SW; Qu SZ; Yang J; Xu H; Bai ZX; Liu N; Kong XD
    Zhonghua Fu Chan Ke Za Zhi; 2018 Jul; 53(7):464-470. PubMed ID: 30078256
    [No Abstract]   [Full Text] [Related]  

  • 12. Sonogenetics in fetal neurology.
    Pooh RK
    Semin Fetal Neonatal Med; 2012 Dec; 17(6):353-9. PubMed ID: 22921277
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Diagnosis of fetal submicroscopic chromosomal abnormalities in failed array CGH samples: copy number by sequencing as an alternative to microarrays for invasive fetal testing.
    Cohen K; Tzika A; Wood H; Berri S; Roberts P; Mason G; Sheridan E
    Ultrasound Obstet Gynecol; 2015 Apr; 45(4):394-401. PubMed ID: 25510919
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Cytogenetic analysis of a complex chromosomal imbalance 14q+ in a fetus featuring multiple congenital defects].
    Li L; Zhou XY; Ji XQ; Yang YQ; Cao L; Zhou J; Liu A; Cheng J; Liu Y; Hu P; Xu ZF
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Apr; 29(2):214-7. PubMed ID: 22487837
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Extracardiac lesions and chromosomal abnormalities associated with major fetal heart defects: comparison of intrauterine, postnatal and postmortem diagnoses.
    Song MS; Hu A; Dyamenahalli U; Chitayat D; Winsor EJ; Ryan G; Smallhorn J; Barrett J; Yoo SJ; Hornberger LK
    Ultrasound Obstet Gynecol; 2009 May; 33(5):552-9. PubMed ID: 19350566
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical utility of array comparative genomic hybridisation in prenatal setting.
    Lovrecic L; Remec ZI; Volk M; Rudolf G; Writzl K; Peterlin B
    BMC Med Genet; 2016 Nov; 17(1):81. PubMed ID: 27846804
    [TBL] [Abstract][Full Text] [Related]  

  • 17. CGH Array and Karyotype as Complementary Tools in Prenatal Diagnosis: Prenatal Diagnosis of a 4q Derivative Chromosome from Maternal 4q;11q Translocation.
    Gonzalez C; Serrano MG; Barbancho Lopez C; Garcia-Riaño T; Barea Calero V; Moreno Perea R; Rodriguez Mogollón B; Queipo Rojas A; Climent AG; Cava Valenciano F
    Fetal Pediatr Pathol; 2018 Jun; 37(3):184-190. PubMed ID: 29771170
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Array comparative genomic hybridization in prenatal diagnosis: another experience.
    Vialard F; Molina Gomes D; Leroy B; Quarello E; Escalona A; Le Sciellour C; Serazin V; Roume J; Ville Y; de Mazancourt P; Selva J
    Fetal Diagn Ther; 2009; 25(2):277-84. PubMed ID: 19521095
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Detection of genomic imbalances by array based comparative genomic hybridisation in fetuses with multiple malformations.
    Le Caignec C; Boceno M; Saugier-Veber P; Jacquemont S; Joubert M; David A; Frebourg T; Rival JM
    J Med Genet; 2005 Feb; 42(2):121-8. PubMed ID: 15689449
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.