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 *

143 related articles for article (PubMed ID: 2325093)

  • 1. Multiple abnormalities in a child with partial duplications of 10p and 13q from a 3:1 segregation of a maternal t(10;13) translocation.
    Yip MY; Williams J; Goddard A; Campbell P; Lambert I; Smithells RW
    J Med Genet; 1990 Mar; 27(3):188-91. PubMed ID: 2325093
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Characterization of familial partial 10p trisomy by chromosomal microdissection, FISH, and microsatellite dosage analysis.
    Stone D; Ning Y; Guan XY; Kaiser-Kupfer M; Wynshaw-Boris A; Biesecker L
    Hum Genet; 1996 Oct; 98(4):396-402. PubMed ID: 8792811
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Family with partial monosomy 10p and trisomy 10p.
    Hon E; Chapman C; Gunn TR
    Am J Med Genet; 1995 Mar; 56(2):136-40. PubMed ID: 7625434
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Deletion 9p, duplication 18q in two sisters resulting from a maternal (9;18) (p22;q21.3) translocation.
    Tayel SM; Kurczynski TW; Casperson S; McCorquodale MM
    Am J Med Genet; 1988 Dec; 31(4):853-61. PubMed ID: 3239578
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Duplication of distal 22q.
    Abeliovich D; Maor E; Bashan N; Carmi R
    Am J Med Genet; 1989 Mar; 32(3):346-9. PubMed ID: 2729354
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Submicroscopic unbalanced translocation resulting in del10p/dup13q detected by subtelomere FISH.
    Roos A; Rudnik-Schöneborn S; Eggermann K; Eggermann T; Senderek J; Schwanitz G; Zerres K; Schüler HM
    Eur J Med Genet; 2006; 49(6):505-10. PubMed ID: 16905374
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Partial duplication 8q12----q21.2 in two sibs with maternally derived insertional and reciprocal translocations: case reports and review of partial duplications of chromosome 8.
    Walker AP; Bocian M
    Am J Med Genet; 1987 May; 27(1):3-22. PubMed ID: 3300332
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A case of de novo translocation 7; 10 and the duplication 7p, deletion 10p phenotype.
    Park JP; McDermet MK; Moeschler JB; Wurster-Hill DH
    Ann Genet; 1993; 36(4):217-20. PubMed ID: 8166428
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Partial monosomy of 10p and duplication of another chromosome in two patients.
    Ohta S; Isojima T; Mizuno Y; Kato M; Mimaki M; Seki M; Sato Y; Ogawa S; Takita J; Kitanaka S; Oka A
    Pediatr Int; 2017 Jan; 59(1):99-102. PubMed ID: 28102624
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Two cases of partial trisomy 10q syndrome due to a familial 10;20 translocation.
    Tüysüz B; Hacihanefioglu S; Silahtaroglu A; Yilmaz S; Deviren A; Cenani A
    Genet Couns; 2000; 11(4):355-61. PubMed ID: 11140413
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Partial duplication 16p resulting from a 3:1 segregation of a maternal reciprocal translocation.
    Mori MA; Gomar JL; Diaz de Bustamante A; Ananias A; Pinel I; Martinez-Frias ML
    Am J Med Genet; 1987 Jan; 26(1):203-6. PubMed ID: 3812563
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Three cases of dup(10p)/del(10q) syndrome resulting from maternal pericentric inversion.
    Kulharya AS; Schneider NR; Wilson GN
    Am J Med Genet; 1993 Nov; 47(6):817-9. PubMed ID: 8279477
    [TBL] [Abstract][Full Text] [Related]  

  • 13. New chromosome aberration: duplication of a large part of chromosome 4q and partial deletion of chromosome 1q.
    Merlob P; Kohn G; Litwin A; Nissenkorn I; Katznelson MB; Reisner SH
    Am J Med Genet; 1989 Jan; 32(1):22-6. PubMed ID: 2705479
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 10p duplication characterized by fluorescence in situ hybridization.
    Wiktor A; Feldman GL; Kratkoczki P; Ditmars DM; Van Dyke DL
    Am J Med Genet; 1994 Sep; 52(3):315-8. PubMed ID: 7528972
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Simultaneous partial monosomy 10p and trisomy 5q in a case of hypoparathyroidism.
    Lai MM; Scriven PN; Ball C; Berry AC
    J Med Genet; 1992 Aug; 29(8):586-8. PubMed ID: 1518027
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Familial translocation t(6;20)(p21;p13) resulting in partial trisomy 6p and partial monosomy 20p: report of a new case and review of the literature.
    Berner AL; Bağci S; Wohlleber E; Engels E; Müller A; Bartmann P; Weber RG; Reutter H
    Cytogenet Genome Res; 2012; 136(4):308-13. PubMed ID: 22433391
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Duplication 16q12----qter arising from 3:1 segregation in a 46,XX,t(13;16) (q12;q12) mother.
    Pérez-Castillo A; Martin-Lucas MA; Abrisqueta JA
    Ann Genet; 1990; 33(2):121-3. PubMed ID: 2241087
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Jumping translocation with partial duplications and triplications of chromosomes 7 and 15.
    Jewett T; Marnane D; Stewart W; Hayworth-Hodge R; Finklea L; Klinepeter K; Rao PN; Pettenati MJ
    Clin Genet; 1998 May; 53(5):415-20. PubMed ID: 9660064
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Inherited chromosomal translocation in two families (t(4q-;13q+) and t(5q-; 13q+)).
    Watanabe G; Kiyoi Y; Takeyama I; Kawana S; Yamamoto M
    Tohoku J Exp Med; 1977 Feb; 121(2):179-84. PubMed ID: 847744
    [TBL] [Abstract][Full Text] [Related]  

  • 20. De novo 13q partial duplication identified by cytogenetic, biochemical and molecular approaches.
    Schwartz S; Harris M; Ehrenpreis R; Zaslav A; Raffel LJ; Schwartz MF; Lieber E; Cohen MM
    Clin Genet; 1991 Dec; 40(6):417-22. PubMed ID: 1778004
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.