254 related articles for article (PubMed ID: 4100531)
1. 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]
2. Trisomy G-21 in adult myelomonocytic leukaemia. An abnormality common to granulocytic and monocytic cells.
Brandt L; Levan G; Mitelman F; Olsson I; Sjögren U
Scand J Haematol; 1974; 12(2):117-22. PubMed ID: 4133853
[No Abstract] [Full Text] [Related]
3. Heterogeneity of Ph1 in chronic myeloid leukaemia.
Mitelman F
Hereditas; 1974; 76(2):315-6. PubMed ID: 4135826
[No Abstract] [Full Text] [Related]
4. The Philadelphia chromosome.
Baserga A; Castoldi GL
Biomedicine; 1973 Mar; 18(2):89-94. PubMed ID: 4125985
[No Abstract] [Full Text] [Related]
5. Letter: A new consistent chromosomal abnormality in chronic myelogenous leukaemia identified by quinacrine fluorescence and Giemsa staining.
Rowley JD
Nature; 1973 Jun; 243(5405):290-3. PubMed ID: 4126434
[No Abstract] [Full Text] [Related]
6. Still more light on human chromosomes.
Nature; 1971 Mar; 230(5290):145. PubMed ID: 4100530
[No Abstract] [Full Text] [Related]
7. Trisomy 21 mosaicism in a woman with two children with trisomy 21 Down's syndrome.
Kaffe S; Hsu LY; Hirschhorn K
J Med Genet; 1974 Dec; 11(4):378-9. PubMed ID: 4140911
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. A case of 47,XX,(21q-)+ with some stigmata of Down's syndrome and an IQ of 77.
Neu RL; Voorhess ML; Gardner LI
J Med Genet; 1971 Dec; 8(4):528-9. PubMed ID: 4261059
[No Abstract] [Full Text] [Related]
11. Down's syndrome transmitted through maternal mosaicism.
Aarskog D
Acta Paediatr Scand; 1969 Nov; 58(6):609-14. PubMed ID: 4244880
[No Abstract] [Full Text] [Related]
12. Identification of the G chromosomes in Down's syndrome by quinacrine fluorescence microscopy.
Alfi OS; Donnell GN; Derencsenyi A
J Pediatr; 1971 Oct; 79(4):656-9. PubMed ID: 4255305
[No Abstract] [Full Text] [Related]
13. 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]
14. Letter: Paternal origin of the extra chromosome in Down's syndrome.
Lancet; 1973 Dec; 2(7840):1257-8. PubMed ID: 4128576
[No Abstract] [Full Text] [Related]
15. Trisomy 9p and unusual translocation mongolism in siblings due to different 3:1 segregations of maternal translocation rcp(9;21)(p11;q11).
Habedank M; Faust J
Hum Genet; 1978 Jun; 42(3):251-6. PubMed ID: 149755
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Paternal trisomy 21 mosaicism and Down's syndrome.
Hsu LY; Gertner M; Leiter E; Hirschhorn K
Am J Hum Genet; 1971 Nov; 23(6):592-601. PubMed ID: 4257130
[No Abstract] [Full Text] [Related]
18. 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]
19. 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]
20. Studies of human chromosomes by DNA-binding fluorochromes. II. Fluorescence characteristics of the supernumerary G chromosome in Down's syndrome.
van der Hagen CB; Berg K
Clin Genet; 1971; 2(1):58-60. PubMed ID: 4255786
[No Abstract] [Full Text] [Related]
[Next] [New Search]