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 *

128 related articles for article (PubMed ID: 38896123)

  • 1. 18q Deletion Syndrome Presenting with Late-Onset Combined Immunodeficiency.
    Hashiguchi S; Tomomasa D; Nishikawa T; Ishikawa S; Akaike H; Kobae H; Shirai T; Nagao T; Noma K; Okada S; Kamuro K; Okamoto Y; Kanegane H
    J Clin Immunol; 2024 Jun; 44(7):154. PubMed ID: 38896123
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Terminal microdeletion of chromosome 18 in a Malaysian boy characterized with few features of typical 18q- deletion syndrome: a case report.
    Ismail A; Ahid F; Thong MK; Zakaria Z
    J Med Case Rep; 2023 Jun; 17(1):250. PubMed ID: 37296475
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Immune Dysregulation in Patients With Chromosome 18q Deletions-Searching for Putative Loci for Autoimmunity and Immunodeficiency.
    Hogendorf A; Zieliński M; Constantinou M; Śmigiel R; Wierzba J; Wyka K; Wędrychowicz A; Jakubiuk-Tomaszuk A; Budzynska E; Piotrowicz M; Lipska-Ziętkiewicz BS; Kaczorowska E; Cieślikowska A; Kutkowska-Kaźmierczak A; Fijak-Moskal J; Kugaudo M; Kosińska-Urbańska M; Szadkowska A; Borowiec M; Niedźwiecki M; Trzonkowski P; Młynarski W
    Front Immunol; 2021; 12():742834. PubMed ID: 34867966
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Chromosome 18q deletion syndrome with autoimmune diabetes mellitus: putative genomic loci for autoimmunity and immunodeficiency.
    Hogendorf A; Lipska-Zietkiewicz BS; Szadkowska A; Borowiec M; Koczkowska M; Trzonkowski P; Drozdz I; Wyka K; Limon J; Mlynarski W
    Pediatr Diabetes; 2016 Mar; 17(2):153-9. PubMed ID: 25403779
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Chromosome 18q-syndrome and 1p terminal duplication in a patient with bilateral vesico-ureteral reflux: case report and literature revision.
    Brandigi E; Molinaro F; Bulotta AL; Angotti R; Pavone M; Messina M
    Ital J Pediatr; 2013 Jan; 39():6. PubMed ID: 23343423
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Craniofacial and Neurological Phenotype in a Patient with De Novo 18q Microdeletion and 18p Microduplication.
    Yapijakis C; Angelopoulou A; Manolakos E; Voumvourakis C
    Adv Exp Med Biol; 2020; 1195():163-166. PubMed ID: 32468472
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Low-level complex mosaic with multiple cell lines affecting the 18q21.31q21.32 region in a patient with de novo 18q terminal deletion.
    Bonaglia MC; Fichera M; Marelli S; Romaniello R; Zuffardi O
    Eur J Med Genet; 2022 Nov; 65(11):104596. PubMed ID: 36064004
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Catathrenia in Pitt-Hopkins syndrome associated with 18q interstitial deletion.
    Motojima T; Fujii K; Ohashi H; Arakawa H
    Pediatr Int; 2018 May; 60(5):479-481. PubMed ID: 29633422
    [No Abstract]   [Full Text] [Related]  

  • 9. Combined deletion 18q22.2 and duplication/triplication 18q22.1 causes microcephaly, mental retardation and leukencephalopathy.
    Nguyen-Minh S; Drossel K; Horn D; Rost I; Spors B; Kaindl AM
    Gene; 2013 Jul; 523(1):92-8. PubMed ID: 23566840
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Terminal deletion of 11q with significant late-onset combined immune deficiency.
    Seppänen M; Koillinen H; Mustjoki S; Tomi M; Sullivan KE
    J Clin Immunol; 2014 Jan; 34(1):114-8. PubMed ID: 24233263
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Intractable epilepsy (apneic seizure) in an infant with 18q deletion syndrome].
    Kumada T; Ito M; Miyajima T; Fujii T; Okuno T; Kumakura A
    No To Hattatsu; 2003 Nov; 35(6):521-6. PubMed ID: 14631750
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Features of two cases with 18q deletion syndrome.
    Özsu E; Mutlu GY; Yüksel AB; Hatun Ş
    J Clin Res Pediatr Endocrinol; 2014; 6(1):51-4. PubMed ID: 24637311
    [TBL] [Abstract][Full Text] [Related]  

  • 13. An 18q- syndrome breakpoint resides between the duplicated serpins SCCA1 and SCCA2 and arises via a cryptic rearrangement with satellite III DNA.
    Katz SG; Schneider SS; Bartuski A; Trask BJ; Massa H; Overhauser J; Lalande M; Lansdorp PM; Silverman GA
    Hum Mol Genet; 1999 Jan; 8(1):87-92. PubMed ID: 9887335
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prenatal diagnosis and molecular cytogenetic characterization of partial dup(18q)/del(18p) due to a paternal pericentric inversion 18 in a fetus with multiple anomalies.
    Lee MJ; Park SH; Shim SH; Moon MJ; Cha DH
    Taiwan J Obstet Gynecol; 2019 May; 58(3):318-323. PubMed ID: 31122516
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Congenital aural atresia in 18q deletion or de Grouchy syndrome.
    Nuijten I; Admiraal R; Van Buggenhout G; Cremers C; Frijns JP; Smeets D; van Ravenswaaij-Arts C
    Otol Neurotol; 2003 Nov; 24(6):900-6. PubMed ID: 14600472
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Interstitial deletion of 18q: comparative genomic hybridization array analysis of 46, XX,del(18)(q21.2.q21.33).
    Kato Z; Morimoto W; Kimura T; Matsushima A; Kondo N
    Birth Defects Res A Clin Mol Teratol; 2010 Feb; 88(2):132-5. PubMed ID: 19813260
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [A girl with partial monosomy 18q21: cytogenetic and molecular genetics studies].
    Lu HY; Cui YX; Shi YC; Xia XY; Yang B; Yao B; Huang YF
    Yi Chuan; 2008 Aug; 30(8):991-5. PubMed ID: 18779147
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Monosomy 18q syndrome and atypical Rett syndrome in a girl with an interstitial deletion (18)(q21.1q22.3).
    Gustavsson P; Kimber E; Wahlström J; Annerén G
    Am J Med Genet; 1999 Feb; 82(4):348-51. PubMed ID: 10051171
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Applying T-cell receptor excision circles and immunoglobulin κ-deleting recombination excision circles to patients with primary immunodeficiency diseases.
    Lee WI; Huang JL; Lin SJ; Yeh KW; Chen LC; Ou LS; Yao TC; Jaing TH; Shih YF; Tseng TY; Lin YL
    Ann Med; 2014 Nov; 46(7):555-65. PubMed ID: 25109505
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Detection of de novo del(18)(q22.2) and a familial of 15q13.2-q13.3 microduplication in a fetus with congenital heart defects.
    Chen CP; Chen CY; Chern SR; Wu PS; Chen SW; Wu FT; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2019 Sep; 58(5):704-708. PubMed ID: 31542097
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.