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    Results: 20

    1.

    Linguistic and psychomotor development in children with chromosome 14 deletions.

    Zampini L, D'Odorico L, Zanchi P, Zollino M, Neri G.

    Clin Linguist Phon. 2012 Dec;26(11-12):962-73. doi: 10.3109/02699206.2012.728669.

    PMID:
    23057796
    [PubMed - indexed for MEDLINE]
    2.

    Segmental paternal uniparental disomy of chromosome 14 in a 4-year-old boy.

    Harrison V, Hurst J, Lloyd-Jani A, Lester T, Lever M, Man S, O'Rourke A, Robinson D, Tabiner M, Williams R, Kini U.

    Clin Dysmorphol. 2012 Oct;21(4):208-11. doi: 10.1097/MCD.0b013e328356da42. No abstract available.

    PMID:
    22797553
    [PubMed - indexed for MEDLINE]
    3.

    A new chromosome 14-based human artificial chromosome (HAC) vector system for efficient transgene expression in human primary cells.

    Kakeda M, Nagata K, Osawa K, Matsuno H, Hiratsuka M, Sano A, Okazaki A, Shitara S, Nishikawa S, Masuya A, Hata T, Wako S, Osaki M, Kazuki Y, Oshimura M, Tomizuka K.

    Biochem Biophys Res Commun. 2011 Nov 25;415(3):439-44. doi: 10.1016/j.bbrc.2011.10.088. Epub 2011 Oct 22.

    PMID:
    22051050
    [PubMed - indexed for MEDLINE]
    4.

    West syndrome associated with mosaic duplication of FOXG1 in a patient with maternal uniparental disomy of chromosome 14.

    Tohyama J, Yamamoto T, Hosoki K, Nagasaki K, Akasaka N, Ohashi T, Kobayashi Y, Saitoh S.

    Am J Med Genet A. 2011 Oct;155A(10):2584-8. doi: 10.1002/ajmg.a.34224. Epub 2011 Sep 9.

    PMID:
    21910242
    [PubMed - indexed for MEDLINE]
    5.

    Cytogenetic and molecular evaluation and 20-year follow-up of a patient with ring chromosome 14.

    Guilherme RS, de Freitas Ayres Meloni V, Sodré CP, Christofolini DM, Pellegrino R, de Mello CB, Conlin LK, Hutchinson AL, Spinner NB, Brunoni D, Kulikowski LD, Melaragno MI.

    Am J Med Genet A. 2010 Nov;152A(11):2865-9. doi: 10.1002/ajmg.a.33689.

    PMID:
    20979193
    [PubMed - indexed for MEDLINE]
    6.

    Evidence for keratoconus susceptibility locus on chromosome 14: a genome-wide linkage screen using single-nucleotide polymorphism markers.

    Liskova P, Hysi PG, Waseem N, Ebenezer ND, Bhattacharya SS, Tuft SJ.

    Arch Ophthalmol. 2010 Sep;128(9):1191-5. doi: 10.1001/archophthalmol.2010.200. Erratum in: Arch Ophthalmol. 2010 Nov;128(11):1431.

    PMID:
    20837804
    [PubMed - indexed for MEDLINE]
    7.

    Duplication of the pituitary stalk in a patient with a heterozygous deletion of chromosome 14 harboring the thyroid transcription factor-1 gene.

    Accornero S, Danesino C, Bastianello S, D'Errico I, Guala A, Chiovato L.

    J Clin Endocrinol Metab. 2010 Aug;95(8):3595-6. doi: 10.1210/jc.2010-0621.

    PMID:
    20685887
    [PubMed - indexed for MEDLINE]
    Free Article
    8.

    Coat hanger appearances of the ribs: a useful diagnostic marker of paternal uniparental disomy of chromosome 14.

    Naik S, Temple IK.

    Arch Dis Child. 2010 Nov;95(11):909. doi: 10.1136/adc.2010.185736. Epub 2010 Jul 23. No abstract available.

    PMID:
    20656731
    [PubMed - indexed for MEDLINE]
    9.

    Partial epilepsy complicated by convulsive and nonconvulsive episodes of status epilepticus in a patient with ring chromosome 14 syndrome.

    Giovannini S, Frattini D, Scarano A, Fusco C, Bertani G, Della Giustina E, Martinelli P, Orteschi D, Zollino M, Neri G, Gobbi G.

    Epileptic Disord. 2010 Sep;12(3):222-7. doi: 10.1684/epd.2010.0324. Epub 2010 Jul 19.

    PMID:
    20643614
    [PubMed - indexed for MEDLINE]
    Free Article
    10.

    Array CGH defined interstitial deletion on chromosome 14: a new case.

    Piccione M, Antona V, Scavone V, Malacarne M, Pierluigi M, Grasso M, Corsello G.

    Eur J Pediatr. 2010 Jul;169(7):845-51. doi: 10.1007/s00431-009-1128-4. Epub 2010 Jan 21.

    PMID:
    20087602
    [PubMed - indexed for MEDLINE]
    11.

    Ring chromosome 14 mosaicism: an unusual case associated with developmental delay and epilepsy, characterized by genome array-CGH.

    Nucaro AL, Falchi M, Pisano T, Rossino R, Boscarelli F, Stoico G, Milia A, Montaldo C, Cianchetti C, Pruna D.

    Am J Med Genet A. 2010 Jan;152A(1):234-6. doi: 10.1002/ajmg.a.33167. No abstract available.

    PMID:
    20034090
    [PubMed - indexed for MEDLINE]
    12.

    Long human CHGA flanking chromosome 14 sequence required for optimal BAC transgenic "rescue" of disease phenotypes in the mouse Chga knockout.

    Vaingankar SM, Li Y, Corti A, Biswas N, Gayen J, O'Connor DT, Mahata SK.

    Physiol Genomics. 2010 Mar 3;41(1):91-101. doi: 10.1152/physiolgenomics.00086.2009. Epub 2009 Dec 15.

    PMID:
    20009010
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    13.

    Chromosome 14 transfer and functional studies identify a candidate tumor suppressor gene, mirror image polydactyly 1, in nasopharyngeal carcinoma.

    Cheung AK, Lung HL, Ko JM, Cheng Y, Stanbridge EJ, Zabarovsky ER, Nicholls JM, Chua D, Tsao SW, Guan XY, Lung ML.

    Proc Natl Acad Sci U S A. 2009 Aug 25;106(34):14478-83. doi: 10.1073/pnas.0900198106. Epub 2009 Aug 10.

    PMID:
    19667180
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    14.

    High-resolution genomic profiling reveals gain of chromosome 14 as a predictor of poor outcome in ileal carcinoids.

    Andersson E, Swärd C, Stenman G, Ahlman H, Nilsson O.

    Endocr Relat Cancer. 2009 Sep;16(3):953-66. doi: 10.1677/ERC-09-0052. Epub 2009 May 20.

    PMID:
    19458023
    [PubMed - indexed for MEDLINE]
    Free Article
    15.

    Chromosome 14 copy number-dependent IGH gene rearrangement patterns in high hyperdiploid childhood B-cell precursor ALL: implications for leukemia biology and minimal residual disease analysis.

    Csinady E, van der Velden VH, Joas R, Fischer S, de Vries JF, Beverloo HB, König M, Pötschger U, van Dongen JJ, Mann G, Haas OA, Panzer-Grümayer ER.

    Leukemia. 2009 May;23(5):870-6. doi: 10.1038/leu.2008.390. Epub 2009 Jan 15.

    PMID:
    19148138
    [PubMed - indexed for MEDLINE]
    16.

    Analysis of selected oncogenes (AKT1, FOS, BCL2L2, TGFbeta) on chromosome 14 in granulosa cell tumors (GCTs): a comprehensive study on 30 GCTs combining comparative genomic hybridization (CGH) and fluorescence-in situ-hybridization (FISH).

    Mayr D, Hirschmann A, Marlow S, Horvath C, Diebold J.

    Pathol Res Pract. 2008;204(11):823-30. doi: 10.1016/j.prp.2008.07.009. Epub 2008 Sep 6.

    PMID:
    18774655
    [PubMed - indexed for MEDLINE]
    17.

    Molecular mechanisms regulating phenotypic outcome in paternal and maternal uniparental disomy for chromosome 14.

    Ogata T, Kagami M, Ferguson-Smith AC.

    Epigenetics. 2008 Jul-Aug;3(4):181-7. Epub 2008 Jul 2. Review.

    PMID:
    18698157
    [PubMed - indexed for MEDLINE]
    Free Article
    18.

    Array-based comparative genomic hybridization of mapped BAC DNA clones to screen for chromosome 14 copy number abnormalities in meningiomas.

    Espinosa AB, Mackintosh C, Maíllo A, Gutierrez L, Sousa P, Merino M, Ortiz J, de Alava E, Orfao A, Tabernero MD.

    Eur J Hum Genet. 2008 Dec;16(12):1450-8. doi: 10.1038/ejhg.2008.128. Epub 2008 Jul 16.

    PMID:
    18628790
    [PubMed - indexed for MEDLINE]
    Free Article
    19.

    Placentomegaly in paternal uniparental disomy for human chromosome 14.

    Kagami M, Yamazawa K, Matsubara K, Matsuo N, Ogata T.

    Placenta. 2008 Aug;29(8):760-1. doi: 10.1016/j.placenta.2008.06.001. Epub 2008 Jul 11. No abstract available.

    PMID:
    18619672
    [PubMed - indexed for MEDLINE]
    20.

    Position effect leading to haploinsufficiency in a mosaic ring chromosome 14 in a boy with autism.

    Castermans D, Thienpont B, Volders K, Crepel A, Vermeesch JR, Schrander-Stumpel CT, Van de Ven WJ, Steyaert JG, Creemers JW, Devriendt K.

    Eur J Hum Genet. 2008 Oct;16(10):1187-92. doi: 10.1038/ejhg.2008.71. Epub 2008 Apr 16.

    PMID:
    18414512
    [PubMed - indexed for MEDLINE]
    Free Article

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