BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

145 related articles for article (PubMed ID: 6715867)

  • 1. Double balanced chromosomal translocation carrier (6;8), (13;14)--a case report: critique and response.
    Young RS
    J Hered; 1984; 75(2):154. PubMed ID: 6715867
    [No Abstract]   [Full Text] [Related]  

  • 2. Ring (13),t(2;6) associated with familial fragile (16).
    Ventruto V; Rinaldi A; Renda S; Stabile M; Rinaldi MM; Cavaliere ML; Conte N; Aveta V
    J Med Genet; 1984 Jun; 21(3):233. PubMed ID: 6748026
    [No Abstract]   [Full Text] [Related]  

  • 3. [A+(8,13) translocation followed for 3 generations].
    Turpin JC; Duc JP; Larget-Piet L; Couturier-Turpin MH; Tamboise A
    Pediatrie; 1981 Sep; 36(6):469-77. PubMed ID: 7312517
    [No Abstract]   [Full Text] [Related]  

  • 4. Fragile site at 12q13 associated with phenotypic abnormalities.
    Morić-Petrović S; Laca Z
    J Med Genet; 1984 Jun; 21(3):216-7. PubMed ID: 6748019
    [TBL] [Abstract][Full Text] [Related]  

  • 5. De novo complex chromosomal rearrangement (CCR) in a severely mentally retarded boy.
    Fryns JP; Kleczkowska A; Kenis H
    Ann Genet; 1984; 27(1):62-4. PubMed ID: 6609678
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Two children with partial trisomy for 7p.
    Berry AC; Honeycombe J; Macoun SJ
    J Med Genet; 1979 Aug; 16(4):320-1. PubMed ID: 490588
    [TBL] [Abstract][Full Text] [Related]  

  • 7. De novo translocation involving chromosomes 2, 8, and 20.
    Zaletajev DV; Marincheva GS; Tsvetkova TG
    J Med Genet; 1984 Jun; 21(3):231. PubMed ID: 6748024
    [No Abstract]   [Full Text] [Related]  

  • 8. Brief clinical report: dup(4p15 leads to 4pter) in a 19-year-old woman resulting from a maternal 4;14 translocation.
    Clark CE; Telfer MA; Cowell HR; Kalamchi A; Steg NL
    Am J Med Genet; 1982 Jan; 11(1):37-42. PubMed ID: 7065001
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Phenotypic disorders in balanced reciprocal translocation: karyotype 46,XY,rcp(13; 21)(q22; q22)].
    Badalian LO; Malygina NA; Gozman TV; Petrukhin AS; Mutovin GR
    Tsitol Genet; 1982; 16(2):17-21. PubMed ID: 7101445
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Monosomy 10qter due to a balanced maternal translocation: t(10;8)(q23;p23).
    Chieri P; Iölster N
    Clin Genet; 1983 Aug; 24(2):147-50. PubMed ID: 6616953
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Trisomy 6q22 leads to 6qter due to maternal 6;21 translocation. Case report review of the literature.
    Taysi K; Chao WT; Monaghan N; Monaco MP
    Ann Genet; 1983; 26(4):243-6. PubMed ID: 6364954
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Wolf-Hirschhorn syndrome and balanced (4;10) translocation in the father.
    Hedner K; Carlsson E; Mitelman F
    Clin Genet; 1977 Aug; 12(2):101-3. PubMed ID: 891010
    [No Abstract]   [Full Text] [Related]  

  • 13. A complex mosaic with tdic(13;18) (p11;p11), +13p-, +18p-, r(13) etc. in a male infant. I. Centromere inactivation and dissociation of dicentric chromosome.
    Uehara M; Kida M
    Jinrui Idengaku Zasshi; 1986 Mar; 31(1):27-35. PubMed ID: 3735756
    [No Abstract]   [Full Text] [Related]  

  • 14. A familial 10/13 translocation: partial trisomy C in an infant associated with familial 10/13 translocation.
    Mulcahy MT; Jenkyn J; Masters PL
    Clin Genet; 1974; 6(5):335-40. PubMed ID: 4434650
    [No Abstract]   [Full Text] [Related]  

  • 15. Autosomal syndromes.
    Summitt RL
    Pediatr Ann; 1978 Jun; 7(6):94-5, 97-100, 102-7 passim. PubMed ID: 149945
    [No Abstract]   [Full Text] [Related]  

  • 16. [Partial 10q trisomy (q24;q ter) caused by a balanced maternal translocation t(6;10)(q26;q24)].
    Aledo AG; Gracia R; López Pajares I; González M; Oliver A; Peralta A
    An Esp Pediatr; 1982 Aug; 17(2):125-9. PubMed ID: 7149479
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Two reciprocal translocations t(9p+;13q-) and t(13q-;21q+): a study of the families.
    Prieto F; Badia L; Asensi F; Roques V
    Hum Genet; 1980; 54(1):7-11. PubMed ID: 7390483
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Phenotype of partial trisomy 8 (p21 leads to qter) in two unrelated patients with de novo translocation.
    Sachs ES; van Waveren G
    J Med Genet; 1981 Jun; 18(3):204-8. PubMed ID: 7241543
    [TBL] [Abstract][Full Text] [Related]  

  • 19. An unbalanced (6q;13q) translocation in a male with clinical features of Ehlers-Danlos type II syndrome.
    Scarbrough PR; Daw J; Carroll AJ; Finley SC
    J Med Genet; 1984 Jun; 21(3):226-8. PubMed ID: 6748022
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Duplication of region 2q31 leads to 2qter in a family with 2/9 translocation.
    Howard-Peebles PN; Goldsmith JP
    Hum Hered; 1980; 30(2):84-8. PubMed ID: 7358400
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.