BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

173 related articles for article (PubMed ID: 5026841)

  • 21. An isochromosome of the short arms of the no. 18 chromosome in a mentally retarded girl.
    Baĺicek P; Zizka J; Lichý J
    Clin Genet; 1976 Feb; 9(2):192-6. PubMed ID: 1248179
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A familial X-22 translocation with an extra X chromosome.
    Jenkins MB; Davis E; Thelen TH; Boyd L
    Am J Hum Genet; 1974 Nov; 26(6):736-45. PubMed ID: 4140689
    [No Abstract]   [Full Text] [Related]  

  • 23. G-deletion syndrome II.
    Chauvel PJ; Schindeler JD; Warren RJ
    Humangenetik; 1972; 14(2):164-6. PubMed ID: 5026850
    [No Abstract]   [Full Text] [Related]  

  • 24. Induction of distinctive chromosomal bands in selected human subjects with D, G, and Y chromosome anomalies.
    Kakati S; Sinha AK
    Hum Hered; 1973 Apr; 23(4):313-30. PubMed ID: 4130026
    [No Abstract]   [Full Text] [Related]  

  • 25. Chromosome aberrations in 50 patients with idiopathic mental retardation and in 50 control subjects. Madison blind study 3.
    Daly RF
    J Pediatr; 1970 Sep; 77(3):444-53. PubMed ID: 5502094
    [No Abstract]   [Full Text] [Related]  

  • 26. An extra small metacentric chromosome in a mentally retarded boy.
    Ishmael J; Laurence KM
    J Med Genet; 1968 Dec; 5(4):335-40. PubMed ID: 5713650
    [No Abstract]   [Full Text] [Related]  

  • 27. Partial monosomy 13 and 21 due to a familial 13/21 translocation.
    Otto PG; Toledo S; Richieri-Costa A; Otto PA; Vianna-Morgante AM; Kasahara S
    Hum Genet; 1978 Apr; 41(3):243-50. PubMed ID: 649151
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Short arm deletion of chromosome 14.
    Emerit I; Noel B; Thiriet M; Loubon M; Quack B
    Humangenetik; 1972; 15(1):33-8. PubMed ID: 5046906
    [No Abstract]   [Full Text] [Related]  

  • 29. Identification of a 18-21 translocation with Klinefelter's syndrome by G-band patterns.
    Waldenmaier C; Hirsch W; König E; Shibata K
    Humangenetik; 1974 Mar; 21(4):323-9. PubMed ID: 4134628
    [No Abstract]   [Full Text] [Related]  

  • 30. Presumed trisomy for the short arm of chromosome No. 9 not due to inherited translocation.
    Hoehn H; Engel W; Reinwein H
    Humangenetik; 1971; 12(3):175-81. PubMed ID: 5563410
    [No Abstract]   [Full Text] [Related]  

  • 31. Deletion long arm 13.
    Nielsen J; Homma A; Christiansen F; Rasmussen K; Saldaña-Garcia P
    Hum Genet; 1977 Jul; 37(3):339-45. PubMed ID: 885554
    [No Abstract]   [Full Text] [Related]  

  • 32. Chromosome studies on male patients at a mental subnormality hospital.
    Aitken J; Brunton M; Jacobs PA; Price WH; MacColl K
    Clin Genet; 1971; 2(6):338-46. PubMed ID: 5155310
    [No Abstract]   [Full Text] [Related]  

  • 33. A Gq deletion in a girl with Down's syndrome.
    Hongell K; Airaksinen E
    Hum Hered; 1972; 22(1):80-5. PubMed ID: 4260912
    [No Abstract]   [Full Text] [Related]  

  • 34. Familial C-G translocation causing mitotic nondisjunction. A cause of familial mosaic Down's syndrome.
    Weiss L; Wolf CB
    Am J Dis Child; 1968 Dec; 116(6):609-14. PubMed ID: 4235163
    [No Abstract]   [Full Text] [Related]  

  • 35. Inherited t(13q14q) in two retarded sisters.
    Crandall BF; Francke U; Campbell MA; Sparkes RS
    Am J Hum Genet; 1972 Jul; 24(4):416-24. PubMed ID: 5031981
    [No Abstract]   [Full Text] [Related]  

  • 36. An inherited small extra chromosome: a mother with 46,XX,t(17;22)(pl;ql) and a son with 47,XY,+der(22)mat.
    Borgaonkar DS; McKusick VA; Farber PA
    J Med Genet; 1973 Dec; 10(4):379-84. PubMed ID: 4129973
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Case report. Familial 4-22 translocation with partial trisomy for the short arm of chromosome 4 in two sibs.
    Sartori A; Tenconi R; Baccichetti C; Pujatti G
    Acta Paediatr Scand; 1974 Jul; 63(4):631-5. PubMed ID: 4850900
    [No Abstract]   [Full Text] [Related]  

  • 38. Partial trisomies of chromosome 21 in man. Two new observations due to translocations 19;21 and 4;21.
    Pfeiffer RA; Kessel EK; Soer KH
    Clin Genet; 1977 Mar; 11(3):207-13. PubMed ID: 138497
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Human chromosome abnormalities as related to physical and mental dysfunction.
    Heller JH
    J Hered; 1969; 60(5):239-48. PubMed ID: 4244249
    [No Abstract]   [Full Text] [Related]  

  • 40. [Sequential staining for G- and C-banding of chromosomes in the analysis of the morphology of the short arms of human acrocentric chromosomes].
    Gurbanov VP; Barkhudarian AS; Malygina NA
    Biull Eksp Biol Med; 1976 Oct; 82(10):1267-9. PubMed ID: 70241
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.