BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

358 related articles for article (PubMed ID: 6748019)

  • 1. 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]  

  • 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. Familial balanced insertion (5;10) and monosomy and trisomy (10) (q24.2----q25.3).
    van de Vooren MJ; Planteydt HT; Hagemeijer A; Peters-Slough MF; Timmerman MJ
    Clin Genet; 1984 Jan; 25(1):52-8. PubMed ID: 6705241
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. A family with craniofrontonasal dysplasia, and fragile site 12q13 segregating independently.
    Kumar D; Clark JW; Blank CE; Patton MA
    Clin Genet; 1986 Jun; 29(6):530-7. PubMed ID: 3742859
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [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]  

  • 8. X;15 translocation in a retarded girl: X inactivation pattern and attempt to localise the hexosaminidase A and other loci.
    Bernstein R; Dawson B; Kohl R; Jenkins T
    J Med Genet; 1979 Aug; 16(4):254-62. PubMed ID: 290816
    [TBL] [Abstract][Full Text] [Related]  

  • 9. X-linked mental retardation with a fragile site in Xq and an inversion of chromosome no. 9.
    Howard-Peebles PN
    Hum Hered; 1982; 32(2):139-41. PubMed ID: 7201453
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Heritable fragility at 11q13 and 12q13.
    Smeets DF; Scheres JM; Hustinx TW
    Clin Genet; 1985 Aug; 28(2):145-50. PubMed ID: 4042396
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Complex translocation in a boy with trichorhinophalangeal syndrome.
    Sánchez LM; Labarta JD; De Negrotti TC; Migliorini AM
    J Med Genet; 1985 Aug; 22(4):314-6. PubMed ID: 4045963
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Fragile site long arm chromosome 16.
    Sørensen K; Nielsen J; Holm V; Haahr J
    Hum Genet; 1979 Apr; 48(1):131-4. PubMed ID: 457128
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A recognizable phenotype in a child with partial duplication 13q in a family with t(10q;13q).
    Hornstein L; Soukup S
    Clin Genet; 1981 Feb; 19(2):81-6. PubMed ID: 7471511
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. Fragile (X)(q27) sites in a pedigree with female carriers showing mild to severe mental retardation.
    Webb GC; Halliday JL; Pitt DB; Judge CG; Leversha M
    J Med Genet; 1982 Feb; 19(1):44-8. PubMed ID: 7069746
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mental retardation and congenital malformations associated with a ring chromosome 9.
    Nakajima S; Yanagisawa M; Kamoshita S; Nakagome Y
    Hum Genet; 1976 Jun; 32(3):289-93. PubMed ID: 939548
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Two different structural abnormalities of chromosome 13 in offspring of chromosomally normal parents with two fragile sites.
    Mules EH; Stamberg J; Jabs EW; Leonard CO
    Clin Genet; 1983 May; 23(5):380-5. PubMed ID: 6851231
    [TBL] [Abstract][Full Text] [Related]  

  • 19. De novo tandem duplication of the middle segment of the long arm of chromosome 14.
    Ito M; Mutoh K; Okuno T; Mikawa H; Edagawa J; Abe T
    Ann Genet; 1983; 26(2):116-9. PubMed ID: 6604486
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Partial trisomy 11 in a child resulting from a complex maternal rearrangement of chromosomes 11, 12 and 13.
    Sanchez O; Yunis JJ; Escobar JI
    Humangenetik; 1974 Apr; 22(1):59-65. PubMed ID: 4134840
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 18.