Letter: Satellite staining of human chromosomes
- PMID: 4138385
- DOI: 10.1016/s0140-6736(74)91097-6
Letter: Satellite staining of human chromosomes
Similar articles
-
Staining of satellite DNA in metaphase chromosomes.Nature. 1971 Jun 25;231(5304):532-3. doi: 10.1038/231532a0. Nature. 1971. PMID: 4103793 No abstract available.
-
Observations with G bonding of human chromosomes. Reduction of dye concentration in Soerensen buffered solutions is sufficient for demonstrating G bands.Humangenetik. 1974;25(1):49-51. Humangenetik. 1974. PMID: 4140841 No abstract available.
-
Cytogenetic aspects of human male meiosis.Adv Hum Genet. 1973;4:327-87. doi: 10.1007/978-1-4615-8261-8_5. Adv Hum Genet. 1973. PMID: 4131530 Review. No abstract available.
-
[Two subterminal heterochromatin regions in a rare form of 21-21 translocation].Humangenetik. 1973;18(4):329-36. doi: 10.1007/BF00291130. Humangenetik. 1973. PMID: 4125993 German. No abstract available.
-
[Study of metaphasic chromosomes by the method of fluorescence (review of the literature)].Probl Gematol Pereliv Krovi. 1974 Mar;19(3):56-60. Probl Gematol Pereliv Krovi. 1974. PMID: 4133967 Review. Russian. No abstract available.
Cited by
-
Partial trisomy 17q. Karyotype: 46,XY,der(21),t(17;21)(q22;p13).Hum Genet. 1979 Jul 18;49(3):361-4. doi: 10.1007/BF00569357. Hum Genet. 1979. PMID: 478542
-
N-band polymorphism of human acrocentric chromosomes and its relevance to satellite association.Hum Genet. 1977 Apr 7;36(1):55-61. doi: 10.1007/BF00390436. Hum Genet. 1977. PMID: 67073
-
Are NORs easily translocated to deleted chromosomes?Hum Genet. 1978 Jun 9;42(2):137-42. doi: 10.1007/BF00283633. Hum Genet. 1978. PMID: 669699
-
Partial trisomy of 11 and 22 due to familial translocation t(11;22)(q23;q11), inherited in three generations.Hum Genet. 1979 Oct 2;51(3):349-55. doi: 10.1007/BF00283408. Hum Genet. 1979. PMID: 511169 No abstract available.
-
Cytogenetic examination of the NOR activity in a proband with 13/13 translocation and in her relatives.Hum Genet. 1978 Sep 19;43(3):275-9. doi: 10.1007/BF00278834. Hum Genet. 1978. PMID: 81168
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources