203 related articles for article (PubMed ID: 4119313)
1. Identification of partial 12 trisomy by quinacrine fluorescence.
Uchida IA; Lin CC
J Pediatr; 1973 Feb; 82(2):269-72. PubMed ID: 4119313
[No Abstract] [Full Text] [Related]
2. Updating advances in cytogenetics. Applications of the new chromosome banding methods.
Breg WR
Birth Defects Orig Artic Ser; 1974; 10(8):7-18. PubMed ID: 4142402
[No Abstract] [Full Text] [Related]
3. 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]
4. 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]
5. Familial translocation involving chromosomes 6, 14 and 20, identified by quinacrine fluorescence.
Allderdice PW; Miller OJ; Miller DA; Breg WR; Gendel E; Zelson C
Humangenetik; 1971; 13(3):205-9. PubMed ID: 5114675
[No Abstract] [Full Text] [Related]
6. Identification of different Robertsonian translocations in man by quinacrine mustard fluorescence analysis.
Caspersson T; Hultén M; Lindsten J; Therkelsen AJ; Zech L
Hereditas; 1971; 67(2):213-20. PubMed ID: 4142007
[No Abstract] [Full Text] [Related]
7. Possible complex translocation t(9;14;13) (q12;pl?;Q31) in mother of a child with 9-p trisomy syndrome.
Fujita H; Abe T; Yamamoto K; Furuyama J
Humangenetik; 1974; 25(2):83-92. PubMed ID: 4140843
[No Abstract] [Full Text] [Related]
8. Quinacrine fluorescence patterns of human D group chromosomes.
Miller DA; Allderdice PW; Miller OJ; Breg WR
Nature; 1971 Jul; 232(5305):24-7. PubMed ID: 4253680
[No Abstract] [Full Text] [Related]
9. Partial Trisomy 1, Karyotype 46,XY,12-,t(1q,12p)+.
Van den Berghe H; Van Eygen M; Fryns JP; Tanghe W; Verresen H
Humangenetik; 1973 May; 18(3):225-30. PubMed ID: 4719634
[No Abstract] [Full Text] [Related]
10. [t(7q-; 21q-plus) and familial and trisomy 21].
Giraud F; Hartung M; Mattei JF; Mattie MG
Ann Genet; 1974 Mar; 17(1):49-53. PubMed ID: 4276449
[No Abstract] [Full Text] [Related]
11. New techniques in the study of human chromosomes: methods and applications.
Dutrillaux B; Lejeune J
Adv Hum Genet; 1975; 5():119-56. PubMed ID: 48327
[No Abstract] [Full Text] [Related]
12. A ring chromosome, diagnosed by quinacrine fluorescence as No. 9, in a mentally retarded girl.
Jacobsen P; Mikkelsen M; Rosleff F
Clin Genet; 1973; 4(5):434-41. PubMed ID: 4127395
[No Abstract] [Full Text] [Related]
13. Banding identification of partial trisomy 15 and of 8/21 translocation.
Wurster-Hill DH; Hoefnagel D
J Ment Defic Res; 1974 Jun; 18(2):139-44. PubMed ID: 4141377
[No Abstract] [Full Text] [Related]
14. A case of partial 14 trisomy 47,XY,(14q-)+ and translocation t(9p+;14q-) in mother and brother.
Short EM; Solitare GB; Breg WR
J Med Genet; 1972 Sep; 9(3):367-73. PubMed ID: 5079109
[No Abstract] [Full Text] [Related]
15. Distinguishing between the chromosomes involved in Down's syndrome (trisomy 21) and cronic myeloid leukaemia (Ph1) by fluorescence.
O'Riordan ML; Robinson JA; Buckton KE; Evans HJ
Nature; 1971 Mar; 230(5290):167-8. PubMed ID: 4100531
[No Abstract] [Full Text] [Related]
16. C8 trisomy mosaicism syndrome.
Bijlsma JB; Wijffels JC; Tegelaers WH
Helv Paediatr Acta; 1972 Jul; 27(3):281-98. PubMed ID: 4645654
[No Abstract] [Full Text] [Related]
17. Partial trisomy in a child with features suggesting mongolism.
Kumbnani HK; Pfeiffer RA
J Med Genet; 1969 Jun; 6(2):201-5. PubMed ID: 4240723
[No Abstract] [Full Text] [Related]
18. Identification of chromosomal abnormalities by quinacrine-staining technique in patients with normal karyotypes by conventional analysis.
del Solar C; Uchida IA
J Pediatr; 1974 Apr; 84(4):534-8. PubMed ID: 4134885
[No Abstract] [Full Text] [Related]
19. Identification of G group anomalies in Down's syndrome by quinacrine dihydrochloride fluorescence staining.
Mikkelsen M
Humangenetik; 1971; 12(1):67-73. PubMed ID: 4104181
[No Abstract] [Full Text] [Related]
20. 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]
[Next] [New Search]