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.
111 related articles for article (PubMed ID: 4264351)
1. Identification of human G-group and Y chromosomes. Demonstration of constitutive heterochromatin by modified DNA-RNA hybridization technique. Cervenka J Clin Genet; 1971; 2(6):375-8. PubMed ID: 4264351 [No Abstract] [Full Text] [Related]
2. Constitutive heterochromatin patterns of G-group chromosomes in Down's syndrome. Pathak S; Sinha AK Humangenetik; 1972; 14(4):327-9. PubMed ID: 4262184 [No Abstract] [Full Text] [Related]
3. Mongolism and sex: a common problem of cell proliferation? Mittwoch U J Med Genet; 1972 Mar; 9(1):92-5. PubMed ID: 4260239 [No Abstract] [Full Text] [Related]
4. Trisomy-21 in mother and child. Report of a case. Friedman JM; Sternberg WH; Varela M; Barclay DL Obstet Gynecol; 1970 Nov; 36(5):731-4. PubMed ID: 4248734 [No Abstract] [Full Text] [Related]
5. Letter: Mongolism by tertiary trisomy. Chaganti RS; Morillo-Cucci G; Degnan M; German J Lancet; 1975 Mar; 1(7908):698-9. PubMed ID: 47133 [No Abstract] [Full Text] [Related]
6. A case of 48,XXY,21+ in an infant with Down's syndrome. Neu RL; Scheuer AQ; Gardner LI J Med Genet; 1971 Dec; 8(4):533-5. PubMed ID: 4260531 [No Abstract] [Full Text] [Related]
7. Prenatal diagnosis of double trisomy. Hsu LY; Strauss L; Alter AV; Kim HJ; Hirschhorn K Am J Dis Child; 1975 Mar; 129(3):381-2. PubMed ID: 123706 [No Abstract] [Full Text] [Related]
8. The sex chromosomes of the Chinese hamster: constitutive heterochromatin deficient in repetitive DNA sequences. Arrighi FE; Hsu TC; Pathak S; Sawada H Cytogenet Cell Genet; 1974; 13(3):268-74. PubMed ID: 4135468 [No Abstract] [Full Text] [Related]
9. Human chromosome identification by differential staining: G goup (21-22-Y). Chernay PR; Hsu LY; Streicher H; Hirschhorn K Cytogenetics; 1971; 10(3):219-24. PubMed ID: 4109910 [No Abstract] [Full Text] [Related]
10. [Identification of group G chromosomes using the heterochromatin method]. Dalecká E; Gregorová B Sb Ved Pr Lek Fak Karlovy Univerzity Hradci Kralove Suppl; 1974; 17(4 Suppl):201-6. PubMed ID: 4283535 [No Abstract] [Full Text] [Related]
11. Distinctive fluorescence of quinacrine-labelled human G group chromosomes. Breg WR; Miller OJ; Miller DA; Allderdice PW Nat New Biol; 1971 Jun; 231(26):276-7. PubMed ID: 4253605 [No Abstract] [Full Text] [Related]
12. 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]
13. Identification by fluorescence of apparently extra human F chromosomes as G chromosomes with giant satellites. Wahlström J Hereditas; 1972; 71(1):154-7. PubMed ID: 4281766 [No Abstract] [Full Text] [Related]
14. Trisomy 21 in a child due to paternal nondisjunction as determined by RFA technique. Verma RS; Dosik H Jinrui Idengaku Zasshi; 1978 Mar; 23(1):17-21. PubMed ID: 78997 [No Abstract] [Full Text] [Related]
15. Down's syndrome with XYY: 48,XYY, G+. al-Aish MS; Dodson WE; Plato CC Am J Dis Child; 1971 May; 121(5):444-6. PubMed ID: 4253705 [No Abstract] [Full Text] [Related]
16. [A case of duplicate 2lp maternal chromosomes in a case of trisomy 21]. Emberger JM; Taib J J Genet Hum; 1975 Oct; 23 SUPPL():98-101. PubMed ID: 129539 [No Abstract] [Full Text] [Related]
17. [Identification of human G chromosomes by the denaturation technique]. Dutrillaux B; Rethoré MO; Prieur M; Raoul O; Berger R; Lejeune J Exp Cell Res; 1972 Feb; 70(2):453-5. PubMed ID: 4110307 [No Abstract] [Full Text] [Related]
18. [Quantitative multienzymatic deficiency and chromosome malsegregation: patients with trisomy 21 and their parents]. Grozdea J; Colombies P; Verdier J Nouv Presse Med; 1973 May; 2(19):1289-91. PubMed ID: 4268234 [No Abstract] [Full Text] [Related]
19. [Down's syndrome with confirmation of trisomy G solely in fibroblast cultures]. Haberlandt W J Genet Hum; 1973 Sep; 21(3):215-22. PubMed ID: 4282491 [No Abstract] [Full Text] [Related]
20. Trisomy E-trisomy G mosaicism. A report of two cases. Bodensteiner JB; Zellweger H Helv Paediatr Acta; 1971 Apr; 26(1):63-70. PubMed ID: 4252807 [No Abstract] [Full Text] [Related] [Next] [New Search]