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 *

255 related articles for article (PubMed ID: 8055322)

  • 41. Prenatal diagnosis of trisomy 21 without the Down syndrome phenotype.
    Aguinaga M; Razo G; Castro J; Mayén-Molina DG
    Prenat Diagn; 2006 Dec; 26(12):1168-71. PubMed ID: 17042031
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Functional analysis of genes implicated in Down syndrome: 1. Cognitive abilities in mice transpolygenic for Down Syndrome Chromosomal Region-1 (DCR-1).
    Chabert C; Jamon M; Cherfouh A; Duquenne V; Smith DJ; Rubin E; Roubertoux PL
    Behav Genet; 2004 Nov; 34(6):559-69. PubMed ID: 15520513
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Cytogenetic analysis of 1572 cases of Down syndrome: a report of double aneuploidy and novel findings 47,XY, t(14;21)(q13;q22.3)mat,+21 and 45,XX,t(14;21) in an Indian population.
    Mandava S; Koppaka N; Bhatia V; Das BR
    Genet Test Mol Biomarkers; 2010 Aug; 14(4):499-504. PubMed ID: 20642367
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Down syndrome with duplication of a region of chromosome 21 containing the CuZn superoxide dismutase gene without detectable karyotypic abnormality.
    Huret JL; Delabar JM; Marlhens F; Aurias A; Nicole A; Berthier M; Tanzer J; Sinet PM
    Hum Genet; 1987 Mar; 75(3):251-7. PubMed ID: 2951317
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Submicroscopic duplication of chromosome 21 and trisomy 21 phenotype (Down syndrome).
    Delabar JM; Sinet PM; Chadefaux B; Nicole A; Gegonne A; Stehelin D; Fridlansky F; Créau-Goldberg N; Turleau C; de Grouchy J
    Hum Genet; 1987 Jul; 76(3):225-9. PubMed ID: 3036686
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Phenotypic and cytogenetic spectrum of 9p trisomy.
    Temtamy SA; Kamel AK; Ismail S; Helmy NA; Aglan MS; El Gammal M; El Ruby M; Mohamed AM
    Genet Couns; 2007; 18(1):29-48. PubMed ID: 17515299
    [TBL] [Abstract][Full Text] [Related]  

  • 47. [Multiple chromosome aberrations in 3 generations of a family and Down's syndrome resulting from partial trisomy of chromosome 21 (q21--q22)].
    Butomo IV; Prozorova MV; Khitrikova LE
    Tsitol Genet; 1984; 18(3):223-8. PubMed ID: 6235655
    [TBL] [Abstract][Full Text] [Related]  

  • 48. The consequences of chromosome imbalance.
    Epstein CJ
    Am J Med Genet Suppl; 1990; 7():31-7. PubMed ID: 2149968
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Complex chromosomal rearrangements of human chromosome 21 in a patient manifesting clinical features partially overlapped with that of Down syndrome.
    Imaizumi T; Yamamoto-Shimojima K; Yanagishita T; Ondo Y; Nishi E; Okamoto N; Yamamoto T
    Hum Genet; 2020 Dec; 139(12):1555-1563. PubMed ID: 32535809
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Highly polymorphic sequence at D21S1448 mapping close to D21S55, within the Down syndrome critical region.
    Hernandez D; Pannett AA; Tybulewicz V; Fisher EM
    Hum Genet; 1995 Jun; 95(6):721-2. PubMed ID: 7789964
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Down's syndrome phenotype and autosomal gene inactivation in a child with presumed (X;21) de novo translocation.
    Taysi K; Sparkes RS; O'Brien TJ; Dengler DR
    J Med Genet; 1982 Apr; 19(2):144-8. PubMed ID: 6210775
    [TBL] [Abstract][Full Text] [Related]  

  • 52. A high resolution physical map of 2.5 Mbp of the Down syndrome region on chromosome 21.
    Patil N; Peterson A; Rothman A; de Jong PJ; Myers RM; Cox DR
    Hum Mol Genet; 1994 Oct; 3(10):1811-7. PubMed ID: 7849705
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Normal phenotype and partial trisomy for the G positive region of chromosome 21.
    Daniel A
    J Med Genet; 1979 Jun; 16(3):227-9. PubMed ID: 157396
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Abnormal chromosome 22 and recurrence of trisomy-22 syndrome.
    Emanuel BS; Zackai EH; Aronson MM; Mellman WJ; Moorhead PS
    J Med Genet; 1976 Dec; 13(6):501-6. PubMed ID: 138742
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Interchange trisomy 21 by t(1;21)(p22;q22)mat.
    Dominguez MG; Rivera H; Vasquez AI; Hernández-Zaragoza G; Rivas F
    Genet Couns; 2001; 12(4):363-7. PubMed ID: 11837606
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Comparative mapping of DNA markers from the familial Alzheimer disease and Down syndrome regions of human chromosome 21 to mouse chromosomes 16 and 17.
    Cheng SV; Nadeau JH; Tanzi RE; Watkins PC; Jagadesh J; Taylor BA; Haines JL; Sacchi N; Gusella JF
    Proc Natl Acad Sci U S A; 1988 Aug; 85(16):6032-6. PubMed ID: 2901095
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Refining chromosomal region critical for Down syndrome-related heart defects with a case of cryptic 21q22.2 duplication.
    Kosaki R; Kosaki K; Matsushima K; Mitsui N; Matsumoto N; Ohashi H
    Congenit Anom (Kyoto); 2005 Jun; 45(2):62-4. PubMed ID: 15904434
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Molecular mapping of 21 features associated with partial monosomy 21: involvement of the APP-SOD1 region.
    Chettouh Z; Croquette MF; Delobel B; Gilgenkrants S; Leonard C; Maunoury C; Prieur M; Rethoré MO; Sinet PM; Chery M
    Am J Hum Genet; 1995 Jul; 57(1):62-71. PubMed ID: 7611297
    [TBL] [Abstract][Full Text] [Related]  

  • 59. A chromosome 21 critical region does not cause specific Down syndrome phenotypes.
    Olson LE; Richtsmeier JT; Leszl J; Reeves RH
    Science; 2004 Oct; 306(5696):687-90. PubMed ID: 15499018
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Partial trisomy 20 (20q13) and partial trisomy 21 (21pter leads to 21q21.3).
    Sanchéz O; Mamunes P; Yunis JJ
    J Med Genet; 1977 Dec; 14(6):459-62. PubMed ID: 146741
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.