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 *

92 related articles for article (PubMed ID: 6226304)

  • 1. Frequency of qh+ chromosomal variants in a) radioexposed, b) Down syndrome and c) control subjects.
    Saccucci F; Catena Q; Dolcini F; Donati D; Magistrelli R; Valentini B; Milani-Comparetti M
    Boll Soc Ital Biol Sper; 1983 Aug; 59(8):1070-5. PubMed ID: 6226304
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Incidence of the qh+ varients in the karyotype of subjects occupationally exposed to ionizing radiations].
    Milani-Comparetti M; Catena Q; Donati D; Magistrelli R; Nataloni P; Saccucci F
    Boll Soc Ital Biol Sper; 1980 Mar; 56(6):549-55. PubMed ID: 7378188
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Frequency of chromosome variants in human populations].
    Kuleshov NP; Kulieva LM
    Genetika; 1979; 15(3):745-51. PubMed ID: 160358
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Incidence of the 9qh+ variant in subjects with occupational exposure to radiation and in cases of reproductive pathology].
    Milani-Comparetti M; Catena Q; Donati D; Magistrelli R; Saccucci F
    Boll Soc Ital Biol Sper; 1981 Feb; 57(4):351-4. PubMed ID: 7195264
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Multiple chromosome aberrations in 3 generations of a family and Down's syndrome resulting from partial trisomy of chromosome 21 (q21--q22)].
    Butomo IV; Prozorova MV; Khitrikova LE
    Tsitol Genet; 1984; 18(3):223-8. PubMed ID: 6235655
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Human chromosomal polymorphism and reproductive function disorder. III. Extreme autosomal C-variants: an analysis of their distribution and combination in the karyotype].
    Tsetkova TG
    Genetika; 1980; 16(12):2210-6. PubMed ID: 7194831
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [C band polymorphisms of chromosomes 1, 9 and 16 in families with children with Down's syndrome (author's transl)].
    Blanco B; Castillo J; Frías S; Carnevale A
    Rev Invest Clin; 1982; 34(1):49-52. PubMed ID: 6211754
    [No Abstract]   [Full Text] [Related]  

  • 8. [Heterochromatic regions of human chromosomes 1, 9, 16 and Y and the phenotype].
    Podgol'nikova OA; Grigor'eva NM; Bliumina MG
    Genetika; 1984 Mar; 20(3):496-500. PubMed ID: 6232170
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Chromosomal polymorphisms of 1, 9, 16, and Y in 4 major ethnic groups: a large prenatal study.
    Hsu LY; Benn PA; Tannenbaum HL; Perlis TE; Carlson AD
    Am J Med Genet; 1987 Jan; 26(1):95-101. PubMed ID: 3812584
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Screening for cytogenetic polymorphisms in a random sample of liveborn infants from Italian population.
    Belloni G; Benincasa A; Bosi A; de Capoa A; Di Castro M; Ferraro M; Lombardi D; Mostacci C; Pelliccia F; Prantera G
    Acta Anthropogenet; 1983; 7(3):205-17. PubMed ID: 6680659
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Polymorphism of the C band of chromosomes in clinical patients].
    Kosztolányi G
    Orv Hetil; 1982 Sep; 123(36):2231-4. PubMed ID: 6890197
    [No Abstract]   [Full Text] [Related]  

  • 12. [Inv(9)(qh): a risk factor in Down's syndrome].
    Serra A; Tedeschi B; Neri G; Sanfilippo S; Bellanova G; Campana M
    Pathologica; 1983; 75 Suppl():243-5. PubMed ID: 6240015
    [No Abstract]   [Full Text] [Related]  

  • 13. Inheritance of a translocation between chromosomes 12 and 16 in a family with recurrent miscarriages and a newborn with Down syndrome carrying the same translocation.
    Pazarbaşi A; Demirhan O; Turgut M; Güzel I; Taştemir D
    Genet Couns; 2008; 19(3):301-8. PubMed ID: 18990986
    [TBL] [Abstract][Full Text] [Related]  

  • 14. C-band heterochromatin polymorphism of human chromosomes 1, 9, 16, Y.
    Simi S; Tursi F
    Boll Soc Ital Biol Sper; 1982 Jul; 58(13):800-6. PubMed ID: 7126351
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Quantitative analysis of the polymorphism of the C-bands of chromosomes 1, 9, 16 and Y in Latvians].
    Krumin' AR; Kroshkina VG
    Tsitol Genet; 1982; 16(4):56-9, 76. PubMed ID: 7135478
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Chromosomal damage in lymphocytes of controls and patients with autosomal and sex-chromosomal disorders.
    Ganguly BB; Talukder G; Sharma A
    Cytobios; 1993; 73(293):95-103. PubMed ID: 8319501
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Human chromosome analysis: methodology and applications.
    Larson L
    Am J Med Technol; 1983 Oct; 49(10):687-98. PubMed ID: 6228140
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Minor chromosomal variants and major chromosomal anomalies in couples with recurrent abortion.
    Blumberg BD; Shulkin JD; Rotter JI; Mohandas T; Kaback MM
    Am J Hum Genet; 1982 Nov; 34(6):948-60. PubMed ID: 7180849
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Chromosomal break points in irradiated and ethyl methane sulphonate treated leucocytes of patients with Down syndrome.
    Reeja TC; Chandra N; Marimuthu KM
    Indian J Exp Biol; 1993 Mar; 31(3):201-5. PubMed ID: 8500834
    [TBL] [Abstract][Full Text] [Related]  

  • 20. High-resolution cytogenetics.
    Yunis JJ; Lewandowski RC
    Birth Defects Orig Artic Ser; 1983; 19(5):11-37. PubMed ID: 6309269
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 5.