These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

111 related articles for article (PubMed ID: 29928177)

  • 1. Interstitial Chromosome 3p13p14 Deletions: An Update and Review.
    Hajek CA; Ji J; Saitta SC
    Mol Syndromol; 2018 May; 9(3):122-133. PubMed ID: 29928177
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Interstitial Chromosome 3p14.1 Deletion due to a Maternal Insertion: Phenotype and Association with Balanced Parental Rearrangement.
    Hajek C; Wang JC; Mahon LW; Martinez A; Saitta SC
    Mol Syndromol; 2016 Apr; 7(1):43-8. PubMed ID: 27194973
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Characterization of a complex chromosomal rearrangement using chromosome, FISH, and microarray assays in a girl with multiple congenital abnormalities and developmental delay.
    Hemmat M; Yang X; Chan P; McGough RA; Ross L; Mahon LW; Anguiano AL; Boris WT; Elnaggar MM; Wang JC; Strom CM; Boyar FZ
    Mol Cytogenet; 2014; 7():50. PubMed ID: 25478007
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Identification of novel deletions of 15q11q13 in Angelman syndrome by array-CGH: molecular characterization and genotype-phenotype correlations.
    Sahoo T; Bacino CA; German JR; Shaw CA; Bird LM; Kimonis V; Anselm I; Waisbren S; Beaudet AL; Peters SU
    Eur J Hum Genet; 2007 Sep; 15(9):943-9. PubMed ID: 17522620
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genomic Investigation of Balanced Chromosomal Rearrangements in Patients with Abnormal Phenotypes.
    Simioni M; Artiguenave F; Meyer V; Sgardioli IC; Viguetti-Campos NL; Lopes Monlleó I; Maciel-Guerra AT; Steiner CE; Gil-da-Silva-Lopes VL
    Mol Syndromol; 2017 Jun; 8(4):187-194. PubMed ID: 28690484
    [TBL] [Abstract][Full Text] [Related]  

  • 6. de novo interstitial deletions at the 11q23.3-q24.2 region.
    Su J; Chen R; Luo J; Fan X; Fu C; Wang J; He S; Hu X; Zhang S; Yi S; Chen S; Shen Y
    Mol Cytogenet; 2016; 9():39. PubMed ID: 27158264
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Consistent interstitial chromosomal deletions in myeloid malignancies and their correlation with fragile sites.
    Hirst WJ; Czepulkowski B; Mufti GJ
    Cancer Genet Cytogenet; 1993 Jan; 65(1):51-7. PubMed ID: 8431916
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Characterization of a 5.8-Mb interstitial deletion of chromosome 3p in a girl with 46,XX,inv(7)dn karyotype and phenotypic abnormalities.
    Morales C; Mademont-Soler I; Armengol L; Milà M; Badenas C; Andrés S; Soler A; Sánchez A
    Cytogenet Genome Res; 2009; 125(4):334-40. PubMed ID: 19864897
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The discovery of microdeletion syndromes in the post-genomic era: review of the methodology and characterization of a new 1q41q42 microdeletion syndrome.
    Shaffer LG; Theisen A; Bejjani BA; Ballif BC; Aylsworth AS; Lim C; McDonald M; Ellison JW; Kostiner D; Saitta S; Shaikh T
    Genet Med; 2007 Sep; 9(9):607-16. PubMed ID: 17873649
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Detection of deletions in de novo "balanced" chromosome rearrangements: further evidence for their role in phenotypic abnormalities.
    Astbury C; Christ LA; Aughton DJ; Cassidy SB; Kumar A; Eichler EE; Schwartz S
    Genet Med; 2004; 6(2):81-9. PubMed ID: 15017330
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Whole Genome Low-Coverage Sequencing Concurrently Detecting Copy Number Variations and Their Underlying Complex Chromosomal Rearrangements by Systematic Breakpoint Mapping in Intellectual Deficiency/Developmental Delay Patients.
    Xiao B; Ye X; Wang L; Fan Y; Gu X; Ji X; Sun Y; Yu Y
    Front Genet; 2020; 11():616. PubMed ID: 32733533
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Interstitial deletion 4p15.32p16.1 and complex chromoplexy in a female proband with severe neurodevelopmental delay, growth failure and dysmorphism.
    Li D; Strong A; Hou C; Downes H; Pritchard AB; Mazzeo P; Zackai EH; Conlin LK; Hakonarson H
    Mol Cytogenet; 2022 Aug; 15(1):33. PubMed ID: 35932041
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A rare case of a boy with de novo microduplication at 5q35.2q35.3 from central Brazil.
    Reis FG; Pinto IP; Minasi LB; Melo AV; Cunha DM; Ribeiro CL; da Silva CC; Silva DM; da Cruz AD
    Genet Mol Res; 2017 Jan; 16(1):. PubMed ID: 28128410
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Chromosomal microarray analysis of infertile men with azoospermia factor microdeletions.
    Zhu Y; Hu L; Cao D; Ou X; Jiang M
    Gene; 2020 Apr; 735():144389. PubMed ID: 31982552
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Nonrandom cytogenetic alterations in hepatocellular carcinoma from transgenic mice overexpressing c-Myc and transforming growth factor-alpha in the liver.
    Sargent LM; Zhou X; Keck CL; Sanderson ND; Zimonjic DB; Popescu NC; Thorgeirsson SS
    Am J Pathol; 1999 Apr; 154(4):1047-55. PubMed ID: 10233843
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Investigation of selected genomic deletions and duplications in a cohort of 338 patients presenting with syndromic obesity by multiplex ligation-dependent probe amplification using synthetic probes.
    D'Angelo CS; Varela MC; de Castro CIe; Kim CA; Bertola DR; Lourenço CM; Perez AB; Koiffmann CP
    Mol Cytogenet; 2014; 7(1):75. PubMed ID: 25411582
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Cytogenetic and fluorescence in situ hybridization characterization of chromosome 1 rearrangements in head and neck carcinomas delineate a target region for deletions within 1p11-1p13.
    Jin Y; Jin C; Wennerberg J; Mertens F; Höglund M
    Cancer Res; 1998 Dec; 58(24):5859-65. PubMed ID: 9865746
    [TBL] [Abstract][Full Text] [Related]  

  • 19. SVAtools for junction detection of genome-wide chromosomal rearrangements by mate-pair sequencing (MPseq).
    Johnson SH; Smadbeck JB; Smoley SA; Gaitatzes A; Murphy SJ; Harris FR; Drucker TM; Zenka RM; Pitel BA; Rowsey RA; Hoppman NL; Aypar U; Sukov WR; Jenkins RB; Feldman AL; Kearney HM; Vasmatzis G
    Cancer Genet; 2018 Feb; 221():1-18. PubMed ID: 29405991
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Balanced chromosomal rearrangements resulting in intellectual disability. An analysis of 22 cases with application of CGH and FISH methods].
    Borg K; Bocian E; Bernaciak J; Nowakowska B; Derwińska K; Obersztyn E; Szczałuba K; Smigiel R; Kostyk E; Mazurczak T
    Med Wieku Rozwoj; 2009; 13(2):81-93. PubMed ID: 19837989
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.