132 related articles for article (PubMed ID: 5055129)
1. Quinacrine fluorescent chromosome analysis of the Snell translocation in the mouse.
Miller DA; Allderdice PW; Kouri RE; Dev VG; Grewal MS; Miller OJ; Hutton JJ
Genetics; 1972 Aug; 71(4):633-7. PubMed ID: 5055129
[TBL] [Abstract][Full Text] [Related]
2. Cattanach's translocation: cytological characterization by quinacrine mustard staining.
Francke U; Nesbitt M
Proc Natl Acad Sci U S A; 1971 Dec; 68(12):2918-20. PubMed ID: 5289234
[TBL] [Abstract][Full Text] [Related]
3. Analysis of the T(3;?)6 Ca and T(14;17)264Ca translocations in the mouse by quinacrine mustard staining.
Nesbitt M; Francke U
Genetics; 1971 Dec; 69(4):517-22. PubMed ID: 4110444
[No Abstract] [Full Text] [Related]
4. Assignment of linkage groups 8 and X to chromosomes in Mus musculus and identification of the centromeric end of linkage group I.
Miller OJ; Miller DA; Kouri RE; Dev VG; Grewal MS; Hutton JJ
Cytogenetics; 1971; 10(6):452-64. PubMed ID: 5146420
[No Abstract] [Full Text] [Related]
5. Quinacrine mustard fluorescence of a second Y chromosome in a Y-autosomal translocation.
Fründ S; Koske-Westphal T; Fuchs-Mecke S; Passarge E
Humangenetik; 1972; 14(2):133-6. PubMed ID: 4112732
[No Abstract] [Full Text] [Related]
6. Linkage groups II and XII of the mouse: cytological localization by fluorochrome staining.
Nesbitt M; Francke U
Science; 1971 Oct; 174(4004):60-2. PubMed ID: 4107692
[TBL] [Abstract][Full Text] [Related]
7. Cytological identification of the chromosomes involved in Searle's translocation and the location of the centromere in the X chromosome of the mouse.
Eicher EM; Nesbitt MN; Francke U
Genetics; 1972 Aug; 71(4):643-8. PubMed ID: 5055131
[TBL] [Abstract][Full Text] [Related]
8. Chromosome markers in Mus musculus: strain differences in C-banding.
Dev VG; Miller DA; Miller OJ
Genetics; 1973 Dec; 75(4):663-70. PubMed ID: 4778788
[TBL] [Abstract][Full Text] [Related]
9. The biarmed chromosomes of mouse cell line LMTK-.
Rushton AR
Can J Genet Cytol; 1973 Dec; 15(4):791-9. PubMed ID: 4798643
[No Abstract] [Full Text] [Related]
10. Studies of human chromosomes by DNA-binding fluorochromes. 3. Detailed analyses of a D-D translocation chromosome--implications for genetic counselling.
van der Hagen CB; Lie T; Berg K
Clin Genet; 1971; 2(3):177-81. PubMed ID: 5111761
[No Abstract] [Full Text] [Related]
11. Quinacrine mustard fluorescence of human chromosomes: characterization of unusual translocations.
Francke U
Am J Hum Genet; 1972 Mar; 24(2):189-213. PubMed ID: 5016511
[No Abstract] [Full Text] [Related]
12. The quinacrine fluorescence karyotype of Mus musculus and demonstration of strain differences in secondary constrictions.
Dev VG; Grewal MS; Miller DA; Kouri RE; Hutton JJ; Miller OJ
Cytogenetics; 1971; 10(6):436-51. PubMed ID: 4111959
[No Abstract] [Full Text] [Related]
13. Identification of the mouse chromosomes by quinacrine mustard staining.
Francke U; Nesbitt M
Cytogenetics; 1971; 10(5):356-66. PubMed ID: 4109887
[No Abstract] [Full Text] [Related]
14. Identification of a C6-G21 translocation chromosome by the Q-M and Giemsa banding techniques in a patient with Down's syndrome, with possible assignment of Gm locus.
Borgaonkar DS; Bias WB; Chase GA; Sadasivan G; Herr HM; Golomb HM; Bahr GF; Kunkel LM
Clin Genet; 1973; 4(1):53-7. PubMed ID: 4120631
[No Abstract] [Full Text] [Related]
15. Banding patterns in mitotic chromosomes of tobacco mouse.
Zech L; Evans EP; Ford CE; Gropp A
Exp Cell Res; 1972 Jan; 70(1):263-8. PubMed ID: 5008404
[No Abstract] [Full Text] [Related]
16. [New technics for chromosome study].
Berger R
Pathol Biol (Paris); 1972 Apr; 20(7):413-24. PubMed ID: 4114329
[No Abstract] [Full Text] [Related]
17. [Identification of several chromosome aberrations in man by the fluorescent method using quinacrine yprite].
Kulikov RI; Mashkova MV; Verlinskaia DK; Bondarev GN
Tsitologiia; 1976 Feb; 18(2):213-8. PubMed ID: 59989
[TBL] [Abstract][Full Text] [Related]
18. Polymorphism of the human Y chromosomes: fluorescence microscopic studies on the sites of morphologic variation.
Tishler PV; Lamborot-Manzur M; Atkins L
Clin Genet; 1972; 3(2):116-22. PubMed ID: 4115479
[No Abstract] [Full Text] [Related]
19. The nature of structural X chromosome aberrations in Turner's syndrome as revealed by quinacrine mustard fluorescence analysis.
Caspersson T; Lindsten J; Zech L
Hereditas; 1970; 66(2):287-92. PubMed ID: 5525826
[No Abstract] [Full Text] [Related]
20. Partial trisomy of chromosome 11: a case report.
Falk RE; Carrel RE; Valente M; Crandall BF; Sparkes RS
Am J Ment Defic; 1973 Jan; 77(4):383-8. PubMed ID: 4706396
[No Abstract] [Full Text] [Related]
[Next] [New Search]