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 *

156 related articles for article (PubMed ID: 8370577)

  • 1. Cytogenetic, FISH and DNA studies in 11 individuals from a family with two siblings with dup(21q) Down syndrome.
    Bartsch O; König U; Petersen MB; Poulsen H; Mikkelsen M; Palau F; Prieto F; Schwinger E
    Hum Genet; 1993 Sep; 92(2):127-32. PubMed ID: 8370577
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular evidence for true isochromosome 21q.
    Priest JH; Blackston RD; Pearse LA; Warren ST
    Hum Genet; 1988 Dec; 81(1):1-3. PubMed ID: 2974012
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Recombinant Down syndrome: a case report and literature review.
    Lazzaro SJ; Speevak MD; Farrell SA
    Clin Genet; 2001 Feb; 59(2):128-30. PubMed ID: 11260215
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Tertiary trisomy due to a reciprocal translocation of chromosomes 5 and 21 in a four-generation family.
    Braddock SR; Henley KM; Potter KL; Nguyen HG; Huang TH
    Am J Med Genet; 2000 Jun; 92(5):311-7. PubMed ID: 10861659
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A Down syndrome case with a karyotype of 46,XY,rec(21)dup(21q)inv(21)(p11q22) derived from paternal pericentric inversion of chromosome 21.
    Ilgin Ruhi H; Tükün A; Karabulut H; Bayazit P; Bökesoy I
    Clin Genet; 2001 May; 59(5):368-70. PubMed ID: 11359472
    [No Abstract]   [Full Text] [Related]  

  • 6. Analysis of DNA polymorphisms suggests that most de novo dup(21q) chromosomes in patients with Down syndrome are isochromosomes and not translocations.
    Antonarakis SE; Adelsberger PA; Petersen MB; Binkert F; Schinzel AA
    Am J Hum Genet; 1990 Dec; 47(6):968-72. PubMed ID: 1978562
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Analysis of pericentromeric chromosome 21 specific YAC clones by FISH: identification of new markers for molecular-cytogenetic application.
    Yurov YB; Laurent AM; Marcais B; Vorsanova SG; Roizes G
    Hum Genet; 1995 Mar; 95(3):287-92. PubMed ID: 7868120
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mirror-symmetric duplicated chromosome 21q with minor proximal deletion, and with neocentromere in a child without the classical Down syndrome phenotype.
    Barbi G; Kennerknecht I; Wöhr G; Avramopoulos D; Karadima G; Petersen MB
    Am J Med Genet; 2000 Mar; 91(2):116-22. PubMed ID: 10748409
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prenatal exclusion of segmental trisomy in familial chromosome 21 pericentric inversion by fluorescence in situ hybridization.
    Tardy EP; Tóth A; Kosztolányi G
    Prenat Diagn; 1997 Sep; 17(9):871-3. PubMed ID: 9316133
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Translocation trisomy dup(21q) and free trisomy 21 can be distinguished by interphase-FISH.
    Liehr T; Starke H; Beensen V; Kähler C; Harbich M; Brude E; Ziegler M; Claussen U
    Int J Mol Med; 1999 Jan; 3(1):11-4. PubMed ID: 9864379
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Application of fluorescence in situ hybridization techniques in clinical genetics: use of two alphoid repeat probes detecting the centromeres of chromosomes 13 and 21 or chromosomes 14 and 22, respectively.
    Kølvraa S; Koch J; Gregersen N; Jensen PK; Jørgensen AL; Petersen KB; Rasmussen K; Bolund L
    Clin Genet; 1991 Apr; 39(4):278-86. PubMed ID: 1829987
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A jumping Robertsonian translocation: a molecular and cytogenetic study.
    Gross SJ; Tharapel AT; Phillips OP; Shulman LP; Pivnick EK; Park VM
    Hum Genet; 1996 Sep; 98(3):291-6. PubMed ID: 8707296
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Study of alpha-satellite DNA in cosmid libraries, specific for chromosomes 13, 21, and 22, using fluorescence in situ hybridization].
    Solov'ev IV; Iurov IuB; Vorsanova SG; Marcais B; Rogaev EI; Kapanadze BI; Brodianskiĭ VM; Iankovskiĭ NK; Roizes G
    Genetika; 1998 Nov; 34(11):1470-9. PubMed ID: 10096024
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Postzygotic isochromosome formation as a cause for false-negative results from chorionic villus chromosome examinations.
    Riegel M; Wisser J; Baumer A; Schinzel A
    Prenat Diagn; 2006 Mar; 26(3):221-5. PubMed ID: 16475225
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Familial transmission of a deletion of chromosome 21 derived from a translocation between chromosome 21 and an inverted chromosome 22.
    Aviv H; Lieber C; Yenamandra A; Desposito F
    Am J Med Genet; 1997 Jun; 70(4):399-403. PubMed ID: 9182781
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Acute myelogenous leukaemia with t(8;21) translocation of normal cell origin in mosaic Down's syndrome with isochromosome 21q.
    Sato A; Imaizumi M; Koizumi Y; Obara Y; Nakai H; Noro T; Saito T; Saisho T; Yoshinari M; Cui Y; Suzuki H; Funato T; Iinuma K
    Br J Haematol; 1997 Mar; 96(3):614-6. PubMed ID: 9054671
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Recurrent abortions and down syndrome resulting from Robertsonian translocation 21q; 21q.
    Kolgeci S; Azemi M; Ahmeti H; Dervishi Z; Sopjani M; Kolgeci J
    Med Arch; 2012; 66(5):350-2. PubMed ID: 23097978
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prenatal diagnosis of isochromosome 21p and isochromosome 21q in a fetus with Down syndrome.
    Yakut S; Sanhal C; Manguoglu E; Cetin Z
    Genet Couns; 2014; 25(3):257-64. PubMed ID: 25365847
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Maternal balanced translocation (4;21) leading to an offspring with partial duplication of 4q and 21q without phenotypic manifestations of Down syndrome.
    El-Ruby M; Hemly NA; Zaki MS
    Genet Couns; 2007; 18(2):217-26. PubMed ID: 17710874
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Clinical, cytogenetic, and molecular evaluation of a patient with partial trisomy 21 (21q11-q22) lacking the classical Down syndrome phenotype.
    Williams CA; Frias JL; McCormick MK; Antonarakis SE; Cantu ES
    Am J Med Genet Suppl; 1990; 7():110-4. PubMed ID: 2149936
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.