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 *

199 related articles for article (PubMed ID: 6447457)

  • 1. C-band polymorphism: comparison between trisomy 21 cases and mentally retarded controls.
    Funderburk SJ; Klisak I; Sparkes RS; Westlake J
    Am J Med Genet; 1980; 5(3):265-9. PubMed ID: 6447457
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Polymorphism of the heterochromatic regions of chromosomes 1, 9, 16 and Y and mental retardation].
    Podugol'nikova OA; Sushanlo KhM; Bliumina MG; Prokof'eva-Bel'govskaia AA
    Genetika; 1984 Jan; 20(1):177-82. PubMed ID: 6538157
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. A case of nondisjunction of chromosome 21 (47,X,Yqs,+21) in an Indian family with Yqs.
    Reddy KS; Thomas IM; Narayanan HS
    Ann Genet; 1984; 27(3):194-6. PubMed ID: 6334487
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Intra-individual polymorphism of human Y chromosome as a result of deletion in the heterochromatin region].
    Nazarenko SA; Nazarenko LP; Baranova VA
    Genetika; 1987 May; 23(5):918-21. PubMed ID: 3623089
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Polymorphism of C-heterochromatin chromosome regions in the etiology of human aneuploidy].
    Kovaleva NV; Butomo IV; Pavlova MN; Khitrikova LE
    Genetika; 1993 Sep; 29(9):1536-43. PubMed ID: 8276221
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. [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]  

  • 9. [Heterochromatic regions and the nondisjunction of human chromosome 21. I. Polymorphism of the C-bands of chromosomes 1, 9 and 16 in children with Down's syndrome].
    Podugol'nikova OA
    Tsitologiia; 1987 Jun; 29(6):711-4. PubMed ID: 2957841
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Heterochromatic regions and chromosome 21 nondisjunction in man. II. A comparative analysis of the polymorphism of the C bands of chromosomes 1, 9 and 16 in the fathers and mothers of Down's disease children].
    Podugol'nikova OA
    Tsitologiia; 1987 Jul; 29(7):848-50. PubMed ID: 2960061
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Q- and C-band polymorphism of the chromosomes in a group of patients with the Shereshevskiĭ-Turner syndrome].
    Tsvetkova TG; Mikhaĭlets LP
    Genetika; 1983 Aug; 19(8):1372-7. PubMed ID: 6685090
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Beckwith-Wiedemann syndrome due to 11p15.5 paternal duplication associated with Klinefelter syndrome and a "de novo" pericentric inversion of chromosome Y.
    Delicado A; Lapunzina P; Palomares M; Molina MA; Galán E; López Pajares I
    Eur J Med Genet; 2005; 48(2):159-66. PubMed ID: 16053907
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Chromosome variation and anomalous karyotypes in the red-backed mouse Clethrionomys rufocanus (Rodentia, Microtinae)].
    Kartavtseva IV; Pavlenko MV; Kostenko VA; Cherniavskiĭ FB
    Genetika; 1998 Aug; 34(8):1106-13. PubMed ID: 9777356
    [TBL] [Abstract][Full Text] [Related]  

  • 14. de novo inversion-duplication of 2q35-2qter without growth retardation.
    Dahoun-Hadorn S; Bretton-Chappuis B
    Ann Genet; 1992; 35(1):55-7. PubMed ID: 1610122
    [TBL] [Abstract][Full Text] [Related]  

  • 15. C-band heterochromatin variants in individuals with neoplastic disorders: carcinoma of breast and ovary.
    Adhvaryu SG; Rawal UM
    Neoplasma; 1991; 38(4):379-84. PubMed ID: 1922570
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Interchromosomal effect leading to an increase in aneuploidy in sperm nuclei in a man heterozygous for pericentric inversion (inv 9) and C-heterochromatin.
    Amiel A; Sardos-Albertini F; Fejgin MD; Sharony R; Diukman R; Bartoov B
    J Hum Genet; 2001; 46(5):245-50. PubMed ID: 11355013
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. The role of Y chromosome C-band size polymorphism in male infertility with a reference to their effect on the total length of the chromosome.
    Yasseen AA; Al-Khafaji SM
    Saudi Med J; 2004 Apr; 25(4):452-5. PubMed ID: 15083214
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Chromosomal polymorphisms due to heterochromatin growth and pericentric inversions in white-bellied rat, Niviventer confucianus, from China.
    Wang JX; Zhao XF; Koh HS; Deng Y; Qi HY
    Hereditas; 2003; 138(1):59-64. PubMed ID: 12830986
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Chromosom al polymorphism in families at risk C-- and Q-- variants in parent and fetal cells].
    Krahulcová A
    Cas Lek Cesk; 1979 May; 118(18):549-54. PubMed ID: 156582
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 10.