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.
143 related articles for article (PubMed ID: 2963417)
1. [Analysis of the inheritance of heterochromatic regions in human chromosomes 1, 9, 16 and Y]. Podugol'nikova OA Tsitol Genet; 1987; 21(5):339-43. PubMed ID: 2963417 [TBL] [Abstract][Full Text] [Related]
2. [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]
3. [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]
4. Analysis of chromosomes in paternity cases. Bujdosó G; Somogyi E Acta Med Leg Soc (Liege); 1989; 39(2):485-98. PubMed ID: 2535401 [TBL] [Abstract][Full Text] [Related]
5. [The C heterochromatin of chromosomes 1, 9, 16 and Y in patients with Noonan's syndrome]. Podugol'nikova OA; Solonichenko VG Tsitol Genet; 1994; 28(3):85-8. PubMed ID: 7974791 [TBL] [Abstract][Full Text] [Related]
6. [Comparative study of methods for the quantitative assessment of the C-segment size of human chromosomes]. Akopian GR Biull Eksp Biol Med; 1987 Mar; 103(3):348-9. PubMed ID: 3828516 [TBL] [Abstract][Full Text] [Related]
7. [A cytogenetic study of the functions of the variable regions in human C heterochromatin. II. C heterochromatin in families with hereditary short stature]. Podugol'nikov OA; Buraia TI; Solonichenko VG Tsitologiia; 1994; 36(11):1041-8. PubMed ID: 7709465 [TBL] [Abstract][Full Text] [Related]
8. [A cytogenetic study of the functions of the variable regions in human C heterochromatin. I. The effect of C heterochromatin on gene expression]. Podugol'nikov OA; Solonichenko VG Tsitologiia; 1994; 36(11):1035-40. PubMed ID: 7709464 [TBL] [Abstract][Full Text] [Related]
9. Heterochromatin is not an adequate explanation for close proximity of interphase chromosomes 1--Y, 9--Y, and 16--Y in human spermatozoa. Tilgen N; Guttenbach M; Schmid M Exp Cell Res; 2001 May; 265(2):283-7. PubMed ID: 11302693 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. [A cytogenetic study of the functions of the variable regions in human C heterochromatin. III. The relationship between the amount of C heterochromatin and the occurrence of the fetal alcohol syndrome]. Podugol'nikov OA; Solonichenko VG Tsitologiia; 1994; 36(11):1049-53. PubMed ID: 7709466 [TBL] [Abstract][Full Text] [Related]
12. [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]
13. [Differential condensation of human chromosomes 9 and Y]. Kovaleva NV; Iakovlev AF Tsitologiia; 1986 Jul; 28(7):720-6. PubMed ID: 3765108 [TBL] [Abstract][Full Text] [Related]
14. [Relation between the size of C-segments and corresponding euchromatic regions of human chromosomes 1, 9 and 16 during their mitotic condensation]. Akopian GR; Sozanskiĭ OA; Guleiuk NL Biull Eksp Biol Med; 1987 Apr; 103(4):454-6. PubMed ID: 3567341 [TBL] [Abstract][Full Text] [Related]
15. [Quantitative analysis of C-segments of chromosomes 1, 9, 16 and Y in couples with reproductive disorders]. Kruminia AR; Kroshkina VG; Voskoboĭnik NI; Reshetnikov AN Genetika; 1987 Mar; 23(3):540-3. PubMed ID: 3569898 [TBL] [Abstract][Full Text] [Related]
16. Immunodeficiency, centromeric heterochromatin instability of chromosomes 1, 9, and 16, and facial anomalies: the ICF syndrome. Maraschio P; Zuffardi O; Dalla Fior T; Tiepolo L J Med Genet; 1988 Mar; 25(3):173-80. PubMed ID: 3351904 [TBL] [Abstract][Full Text] [Related]
17. [Quantitative characteristics of heterochromatin regions in human metaphase chromosomes at different stages of ontogenesis]. Akopian GR; Sozans'kyĭ OO; Gavryliuk Iuĭ Tsitol Genet; 1992; 26(4):50-5. PubMed ID: 1440918 [TBL] [Abstract][Full Text] [Related]
18. [Variability of the heterochromatic regions of human chromosomes 1, 9, 16, and Y]. Podugol'nikova OA; Sushanlo KhM; Parfenova IV; Prokof'eva-Bel'govskaia AA Genetika; 1980 Apr; 16(4):720-6. PubMed ID: 7192240 [TBL] [Abstract][Full Text] [Related]
19. [Heteromorphism of chromosome 1, 9 and 16 homologs in persons living in regions differing in the level of longevity]. Kuznetsova SM; Zaritskaia MIu; Berdyshev GD Tsitol Genet; 1988; 22(4):27-32. PubMed ID: 2973673 [TBL] [Abstract][Full Text] [Related]