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567 related items for PubMed ID: 19521095

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

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  • 4. Prenatal diagnosis of a 9q34.3 microdeletion by array-CGH in a fetus with an apparently balanced translocation.
    Simovich MJ, Yatsenko SA, Kang SH, Cheung SW, Dudek ME, Pursley A, Ward PA, Patel A, Lupski JR.
    Prenat Diagn; 2007 Dec; 27(12):1112-7. PubMed ID: 17849500
    [Abstract] [Full Text] [Related]

  • 5. Prenatal diagnosis by array-CGH.
    Rickman L, Fiegler H, Carter NP, Bobrow M.
    Eur J Med Genet; 2005 Dec; 48(3):232-40. PubMed ID: 16179219
    [Abstract] [Full Text] [Related]

  • 6. Cryptic genomic imbalances in de novo and inherited apparently balanced chromosomal rearrangements: array CGH study of 47 unrelated cases.
    Schluth-Bolard C, Delobel B, Sanlaville D, Boute O, Cuisset JM, Sukno S, Labalme A, Duban-Bedu B, Plessis G, Jaillard S, Dubourg C, Henry C, Lucas J, Odent S, Pasquier L, Copin H, Latour P, Cordier MP, Nadeau G, Till M, Edery P, Andrieux J.
    Eur J Med Genet; 2009 Dec; 52(5):291-6. PubMed ID: 19505601
    [Abstract] [Full Text] [Related]

  • 7. De novo 16p13.11 microdeletion identified by high-resolution array CGH in a fetus with increased nuchal translucency.
    Law LW, Lau TK, Fung TY, Leung TY, Wang CC, Choy KW.
    BJOG; 2009 Jan; 116(2):339-43. PubMed ID: 19018765
    [Abstract] [Full Text] [Related]

  • 8. Detection of known and novel genomic rearrangements by array based comparative genomic hybridisation: deletion of ZNF533 and duplication of CHARGE syndrome genes.
    Monfort S, Roselló M, Orellana C, Oltra S, Blesa D, Kok K, Ferrer I, Cigudosa JC, Martínez F.
    J Med Genet; 2008 Jul; 45(7):432-7. PubMed ID: 18413373
    [Abstract] [Full Text] [Related]

  • 9. A retrospective study by oligonucleotide array-CGH analysis in 50 fetuses with multiple malformations.
    Valduga M, Philippe C, Bach Segura P, Thiebaugeorges O, Miton A, Beri M, Bonnet C, Nemos C, Foliguet B, Jonveaux P.
    Prenat Diagn; 2010 Apr; 30(4):333-41. PubMed ID: 20155755
    [Abstract] [Full Text] [Related]

  • 10. Copy number imbalances detected with a BAC-based array comparative genomic hybridization platform in congenital diaphragmatic hernia fetuses.
    Machado IN, Heinrich JK, Barini R, Peralta CF.
    Genet Mol Res; 2011 Feb 15; 10(1):261-7. PubMed ID: 21341218
    [Abstract] [Full Text] [Related]

  • 11. Genetic diagnosis by comparative genomic hybridization in adult de novo acute myelocytic leukemia.
    Casas S, Aventín A, Fuentes F, Vallespí T, Granada I, Carrió A, Angel Martínez-Climent J, Solé F, Teixidó M, Bernués M, Duarte J, Maria Hernández J, Brunet S, Dolors Coll M, Sierra J.
    Cancer Genet Cytogenet; 2004 Aug 15; 153(1):16-25. PubMed ID: 15325089
    [Abstract] [Full Text] [Related]

  • 12. De novo monosomy 9p24.3-pter and trisomy 17q24.3-qter characterised by microarray comparative genomic hybridisation in a fetus with an increased nuchal translucency.
    Brisset S, Kasakyan S, L'Herminé AC, Mairovitz V, Gautier E, Aubry MC, Benkhalifa M, Tachdjian G.
    Prenat Diagn; 2006 Mar 15; 26(3):206-13. PubMed ID: 16450348
    [Abstract] [Full Text] [Related]

  • 13. Comparison of comparative genomic hybridization with conventional karyotype and classical fluorescence in situ hybridization for prenatal and postnatal diagnosis of unbalanced chromosome abnormalities.
    Lapierre JM, Cacheux V, Collot N, Da Silva F, Hervy N, Rivet D, Romana S, Wiss J, Benzaken B, Aurias A, Tachdjian G.
    Ann Genet; 1998 Mar 15; 41(3):133-40. PubMed ID: 9833066
    [Abstract] [Full Text] [Related]

  • 14. 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 15; 16(12):1450-8. PubMed ID: 18628790
    [Abstract] [Full Text] [Related]

  • 15. Subtelomeric rearrangements and 22q11.2 deletion syndrome in anomalous growth-restricted fetuses with normal or balanced G-banded karyotype.
    Chen M, Hwu WL, Kuo SJ, Chen CP, Yin PL, Chang SP, Lee DJ, Chen TH, Wang BT, Lin CC.
    Ultrasound Obstet Gynecol; 2006 Dec 15; 28(7):939-43. PubMed ID: 17121426
    [Abstract] [Full Text] [Related]

  • 16. [A preliminary study to assess the value of the DNA chips SpectralChip to detect subtle constitutional chromosome imbalances].
    Lapierre JM, Sanlaville D, Kang J, Ozilou C, Le Lorc'h M, Waill MC, Prieur M, Colleaux L, Munnich A, Turleau C, Benkhalifa M, Mohammed M, Vekemans M, Romana S.
    Ann Biol Clin (Paris); 2004 Dec 15; 62(2):203-12. PubMed ID: 15047473
    [Abstract] [Full Text] [Related]

  • 17. 8p23.1 duplication syndrome; a novel genomic condition with unexpected complexity revealed by array CGH.
    Barber JC, Maloney VK, Huang S, Bunyan DJ, Cresswell L, Kinning E, Benson A, Cheetham T, Wyllie J, Lynch SA, Zwolinski S, Prescott L, Crow Y, Morgan R, Hobson E.
    Eur J Hum Genet; 2008 Jan 15; 16(1):18-27. PubMed ID: 17940555
    [Abstract] [Full Text] [Related]

  • 18. Prenatal diagnosis of de novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements.
    Chen CP, Chern SR, Lee CC, Lin CC, Li YC, Hsieh LJ, Chen WL, Wang W.
    Prenat Diagn; 2006 Feb 15; 26(2):138-46. PubMed ID: 16470734
    [Abstract] [Full Text] [Related]

  • 19. De novo subtelomeric deletion additional to an inherited apparently balanced reciprocal translocation.
    Delahaye A, Pipiras E, Kanafani S, Touboul C, Vergnaud A, Encha-Razavi F, Sinico M, Benkhalifa M, Kasakyan S, Serero S, Wolf JP, Gérard-Blanluet M, Benzacken B.
    Fetal Diagn Ther; 2007 Feb 15; 22(4):306-12. PubMed ID: 17361086
    [Abstract] [Full Text] [Related]

  • 20. High frequency of submicroscopic genomic aberrations detected by tiling path array comparative genome hybridisation in patients with isolated congenital heart disease.
    Erdogan F, Larsen LA, Zhang L, Tümer Z, Tommerup N, Chen W, Jacobsen JR, Schubert M, Jurkatis J, Tzschach A, Ropers HH, Ullmann R.
    J Med Genet; 2008 Nov 15; 45(11):704-9. PubMed ID: 18713793
    [Abstract] [Full Text] [Related]

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