about
The Giemsa C-Banded Karyotype of RyeFertile mule in China and her unusual foalIdentification of human RNA transcripts among heterogeneous nuclear RNA from man-mouse somatic cell hybridsSatellite DNA.Differences in human X isochromosomes.Two pericentric inversions of human chromosome 11Length heteromorphisms of fluorescent (f) and non-fluorescent (nf) segments of human Y chromosome: classification, frequencies, and incidence in normal Caucasians.X-Y translocation in a retarded phenotypic male. Clinical, cytogenetic, biochemical, and serogenetic studies.High resolution of a small pericentric inversion of chromosome 11.45,X/46,XY/47,XY, +21 mosaicism in a hypogonadal phenotypic male.New C band markers of human chromosomes: C band position variants.Homodicentric chromosomes: a distinctive type of dicentric chromosome.A 13-year-old girl with karyotype 47, XX, +i (22) (qll).Human chromosomal heteromorphisms in American blacks. VI. Higher incidence of longer Y owing to non-fluorescent (nf) segment.Report of a new case and clinical delineation of mosaic trisomy 9 syndrome.Spatial relationship of human X and Y chromosomes at somatic metaphase.The X chromosomes of mammals: karylogical homology as revealed by banding techniques.Heterochromatin and satellite DNA in man: properties and prospects.Development and application of camelid molecular cytogenetic tools.Hidden heterochromatin: Characterization in the Rodentia species Cricetus cricetus, Peromyscus eremicus (Cricetidae) and Praomys tullbergi (Muridae).48,XYYY: a new syndrome?Giemsa banding pattern of a heritable 1q+ variant chromosome: a possible partial duplication.The use of new staining techniques for human chromosome identificationUses of banding techniques for the identification of human diseases of cytogenetic origin.Assignment of three human genes to chromosomes (LDH-A to 11, TK to 17, and IDH to 20) and evidence for translocation between human and mouse chromosomes in somatic cell hybrids (thymidine kinase-lactate dehydrogenase A-isocitrate dehydrogenase-C-11,Compositional heterogeneity of human heterochromatin.DNA profiling of B chromosomes from the yellow-necked mouse Apodemus flavicollis (Rodentia, Mammalia).Lymphocyte chromosomal aberration assay in radiation biodosimetry.Differenial chromosome staining.Chromosome 15 abnormalities and the Prader-Willi syndrome: a follow-up report of 40 cases.Patterns of DNA replication of human chromosomes. II. Replication map and replication model.Lateral asymmetry in human constitutive heterochromatin: frequency and inheritancePolymorphism of human C-band heterochromatin. I. Frequency of variantsCytogenetic and linkage studies of a familial 15pplus variant.Pericentric inversions of human chromosomes 9 and 10.Recent advances in cytogenetics and their relevance to medicineIdentity of tumorigenic human urothelial cell lines and 'spontaneously' transformed sublines.The chromosomes of man--clinical and biologic significance. A review.Relationship of chromosome changes to neoplastic cell transformation.Chromosome studies in man: past achievements and recent advances
P2860
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P2860
description
1971 nî lūn-bûn
@nan
1971年の論文
@ja
1971年学术文章
@wuu
1971年学术文章
@zh-cn
1971年学术文章
@zh-hans
1971年学术文章
@zh-my
1971年学术文章
@zh-sg
1971年學術文章
@yue
1971年學術文章
@zh
1971年學術文章
@zh-hant
name
Localization of heterochromatin in human chromosomes.
@en
Localization of heterochromatin in human chromosomes.
@nl
type
label
Localization of heterochromatin in human chromosomes.
@en
Localization of heterochromatin in human chromosomes.
@nl
prefLabel
Localization of heterochromatin in human chromosomes.
@en
Localization of heterochromatin in human chromosomes.
@nl
P1433
P1476
Localization of heterochromatin in human chromosomes.
@en
P2093
P577
1971-01-01T00:00:00Z