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 *

91 related articles for article (PubMed ID: 10378408)

  • 1. 18q-syndrome with coeliac disease.
    Lipschutz W; Cadranel S; Lipschutz B; Martin L; Clees N; Martin JJ; Wauters JG; Coucke P; Willems P
    Eur J Pediatr; 1999 Jun; 158(6):528. PubMed ID: 10378408
    [No Abstract]   [Full Text] [Related]  

  • 2. Mosaic isodicentric chromosome 18q: sixth report and review.
    Oudesluijs GG; Hulzebos CV; Sikkema-Raddatz B; Van Essen AJ
    Genet Couns; 2006; 17(4):395-400. PubMed ID: 17375524
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Ablepharon macrostomia syndrome with associated cutis laxa: possible localization to 18q.
    Pellegrino JE; Schnur RE; Boghosian-Sell L; Strathdee G; Overhauser J; Spinner NB; Stump T; Grace K; Zackai EH
    Hum Genet; 1996 Apr; 97(4):532-6. PubMed ID: 8834257
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Analysis of clinical variation seen in patients with 18q terminal deletions.
    Strathdee G; Zackai EH; Shapiro R; Kamholz J; Overhauser J
    Am J Med Genet; 1995 Dec; 59(4):476-83. PubMed ID: 8585568
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prenatal detection of trisomy 18 caused by isochromosome 18p and 18q formation.
    van den Berg C; Pijpers L; Halley DJ; Opstal DV; Los FJ
    Am J Med Genet; 1999 Sep; 86(2):151-5. PubMed ID: 10449651
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genome-wide linkage analysis for celiac disease in North American families.
    Neuhausen SL; Feolo M; Camp NJ; Farnham J; Book L; Zone JJ
    Am J Med Genet; 2002 Jul; 111(1):1-9. PubMed ID: 12124726
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Precocious puberty associated with partial trisomy 18q and monosomy 11q.
    Mutesa L; Hellin AC; Jamar M; Pierquin G; Bours V; Verloes A
    Genet Couns; 2007; 18(2):201-7. PubMed ID: 17710872
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Partial trisomy 18q11.2-->qter due to de novo unbalanced translocation of chromosomes 15 and 18 analyzed by fluorescence in situ hybridization.
    Semerci CN; Bahce M; Atik F; Candemir Z; Kiraz IK; Zorlu P; Gül D
    Ann Genet; 2004; 47(4):393-8. PubMed ID: 15581838
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Cytogenetic investigation of a child with a mosaic isochromosome 18q and ring 18q.
    Souraty N; Sanlaville D; Chédid R; Le Lorc'h M; Maurin ML; Ghanem L; Maalouf S; Vekemans M; Mégarbané A
    Eur J Med Genet; 2007; 50(5):379-85. PubMed ID: 17716964
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Linkage analysis of candidate regions for coeliac disease genes.
    Houlston RS; Tomlinson IP; Ford D; Seal S; Marossy AM; Ferguson A; Holmes GK; Hosie KB; Howdle PD; Jewell DP; Godkin A; Kerr GD; Kumar P; Logan RF; Love AH; Johnston S; Marsh MN; Mitton S; O'Donoghue D; Roberts A; Walker-Smith JA; Stratton MF
    Hum Mol Genet; 1997 Aug; 6(8):1335-9. PubMed ID: 9259281
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Chromosome 18 replaced by two ring chromosomes of chromosome 18 origin.
    Miller K; Pabst B; Ritter H; Nürnberg P; Siebert R; Schmidtke J; Arslan-Kirchner M
    Hum Genet; 2003 Apr; 112(4):343-7. PubMed ID: 12574939
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Isochromosome 18q in a girl with holoprosencephaly, DiGeorge anomaly, and streak ovaries.
    van Essen AJ; Schoots CJ; van Lingen RA; Mourits MJ; Tuerlings JH; Leegte B
    Am J Med Genet; 1993 Aug; 47(1):85-8. PubMed ID: 8368259
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [A case of Noonan Syndrome with coeliac disease due to SOS1 mutation].
    Carcavilla Urquí A; Santomé Collazo JL; Barrio Castellanos R; Ezquieta Zubicaray B
    Med Clin (Barc); 2011 Nov; 137(14):666-7. PubMed ID: 21524768
    [No Abstract]   [Full Text] [Related]  

  • 15. Mosaic chromosome 18q partial deletion syndrome with bilateral full-thickness corneal disease: surgical intervention and histopathology.
    Galvin JA; LeBoyer RM; Michelotti M; Monte MA; Elner VM; Mian SI
    Ophthalmic Genet; 2015 Mar; 36(1):75-8. PubMed ID: 24024746
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [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]  

  • 17. Evaluation of cytokine polymorphisms (TNFalpha, IFNgamma and IL-10) in Down patients with coeliac disease.
    Cataldo F; Scola L; Piccione M; Giuffrè M; Crivello A; Forte GI; Lio D; Corsello G
    Dig Liver Dis; 2005 Dec; 37(12):923-7. PubMed ID: 16182624
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular cloning and RARE cleavage mapping of human 2p, 6q, 8q, 12q, and 18q telomeres.
    Macina RA; Morii K; Hu XL; Negorev DG; Spais C; Ruthig LA; Riethman HC
    Genome Res; 1995 Oct; 5(3):225-32. PubMed ID: 8593610
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mapping susceptibility gene locus for IgA deficiency at del(18)(q22.3-q23); report of familial cryptic chromosome t(18q; 10p) translocations.
    Dostal A; Linnankivi T; Somer M; Kähkönen M; Litzman J; Tienari P
    Int J Immunogenet; 2007 Jun; 34(3):143-7. PubMed ID: 17504501
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Genotype and phenotype analysis of a child with partial 18q deletion syndrome].
    Shi S; Guo L; Zha Q; Shi Z; Yang Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Aug; 34(4):567-570. PubMed ID: 28777861
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.