| scholarly article | Q13442814 |
| P356 | DOI | 10.1007/BF00295805 |
| P698 | PubMed publication ID | 903153 |
| P2093 | author name string | S. R. Patil | |
| H. A. Lubs | |||
| P2860 | cites work | Giemsa banding pattern of a heritable 1q+ variant chromosome: a possible partial duplication | Q34634863 |
| Polymorphism of human C-band heterochromatin. I. Frequency of variants | Q35569920 | ||
| Polymporphism of human C-band heterochromatin. II. Family studies with suggestive evidence for somatic crossing over | Q35570512 | ||
| Letter: A1 and C9 marker chromosomes in children with combined minor and major malformations | Q39315271 | ||
| Chromosome 16 heterology. Nonspecific variation in karyotype? | Q53995591 | ||
| Localization of heterochromatin in human chromosomes. | Q54215761 | ||
| Human Q and C chromosomal variations: distribution and incidence | Q66956192 | ||
| Chromosome polymorphism in a human newborn population. II. Potentials of polymorphic chromosome variants for characterizing the idiogram of an individual | Q67377583 | ||
| C- and Q-band polymorphisms in the chromosomes of three human populations | Q67806019 | ||
| The nature and inheritance of an elongated secondary constriction on chromosome 9 of man | Q70017296 | ||
| 1q plus variants in a normal adult population (one with a pericentric inversion) | Q70028945 | ||
| An analysis of the technical variables in the production of C bands | Q93735261 | ||
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 35-38 | |
| P577 | publication date | 1977-08-01 | |
| 1977-08-31 | |||
| P1433 | published in | Human Genetics | Q5937167 |
| P1476 | title | Classification of qh regions in human chromosomes 1, 9, and 16 by C-banding | |
| P478 | volume | 38 |
| Q66864533 | A comment on the paper: Reciprocal translocation and the Philadelphia chromosome By Jessie L. Watt and Brenda M. Page, Hum. Genet. 42, 163?170 (1978) |
| Q71827048 | A deletion of heterochromatin only of the Y chromosome in an azoospermic male |
| Q45684495 | A new approach in the evaluation of C-positive variants in man |
| Q70683881 | A new approach in the evaluation of chromosome variants in man, III. Pairs with established Q or C variable sites |
| Q71438256 | A new approach in the evaluation of chromosome variants in man. II. Pairs without Q or C (qh) variants |
| Q70338513 | An attempt to define 1qh+, 9qh+, and 16qh+ |
| Q69217808 | C-band polymorphisms of chromosome 9: quantification by Ce-bands |
| Q90244644 | C-banding and AgNOR-staining were still effective complementary methods to indentify chromosomal heteromorphisms and some structural abnormalities in prenatal diagnosis |
| Q41675239 | Cancer family syndrome: cytogenetic investigations, in vitro tetraploidy, and biomarker studies in a large family. |
| Q52106744 | Chromosomal variants in mentally retarded and normal men |
| Q41471249 | Constitutive heterochromatin studies in patients with solid tumors |
| Q70683892 | Cytogenetic study of a large black kindred: inversions, heteromorphisms, and segregation analysis |
| Q70646313 | Heterochromatin and nucleolus organizer regions in cells of patients with malignant and premalignant lymphatic diseases |
| Q40097678 | Human Chromosomal Heteromorphisms: Nature and Clinical Significance |
| Q44033805 | Human chromosomal polymorphism. II. Chromsomal C polymorphism in Mongoloid populations of central Asia |
| Q41489793 | Mitomycin C-induced mosaicism in C-band regions of human chromosomes 1, 9, 16, and Y. |
| Q70587561 | Polymorphism of human chromosomes 1, 9, 16, Y: variations, segregation and mosaicism |
| Q70683912 | Q- and C-band polymorphisms in patients with ovarian or breast carcinoma |
| Q71065662 | Quantification of C-band polymorphisms by centromeric elevations (Ce-bands) |
| Q72830364 | Relationship of the variability of the heterochromatic regions of chromosomes 1, 9, 16, and Y to some anthropometric characteristics in children with embryopathies of unknown etiology and in children with Down syndrome |
| Q40468551 | Size and pericentric inversion heteromorphisms of secondary constriction regions (h) of chromosomes 1, 9, and 16 as detected by CBG technique in Caucasians: Classification, frequencies, and incidence |
| Q47269936 | The quantitative analysis of constitutive heterochromatic regions of human chromosomes 1, 9, and 16 in relation to size and inversion heteromorphisms in East Indians |
| Q70649756 | The quantitative analysis of polymorphism on human chromosomes 1,9,16, and Y. IV. Heterogeneity of a normal population |
| Q67404262 | Types and frequencies of Q-variant chromosomes in a Japanese population |
| Q40910498 | Variability and familial transmission of constitutive heterochromatin of human chromosomes evaluated by the method of linear measurement |
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