| P2093 | author name string | I Hansmann | |
| | T Grimm | |
| | M Geisler | |
| P2860 | cites work | Family studies on the chromosomal location of the retinoblastoma gene (Rb-1). | Q33669440 |
| | Familial retinoblastoma: segregation of chromosome 13 in four families. | Q35203655 |
| | Polymporphism of human C-band heterochromatin. II. Family studies with suggestive evidence for somatic crossing over | Q35570512 |
| | Twins and Q-banded chromosome polymorphisms | Q43583639 |
| | Origin of the extra chromosome in trisomy 16 | Q44398682 |
| | The status of the gene map of the human chromosomes | Q51051769 |
| | Polymorphism in chromosome 4 | Q52101421 |
| | A rapid banding technique for routine use in human and comparative cytogenetics. | Q53719766 |
| | Human Q and C chromosomal variations: distribution and incidence | Q66956192 |
| | Trisomy 21 in man due to maternal non-disjunction during the first meiotic division | Q68543861 |
| | A new genetic concept: uniparental disomy and its potential effect, isodisomy | Q70656134 |
| | Quinacrine mustard and nucleolar organizer region heteromorphisms in twins | Q70674549 |
| | Transmission of a balanced homologous t(22q;22q) translocation from mother to normal daughter | Q71263512 |
| | Habitual abortion and translocation (22q;22q): unexpected transmission from a mother to her phenotypically normal daughter | Q71433516 |
| | A simple technique for demonstrating centromeric heterochromatin | Q93730570 |
| P433 | issue | 4 | |
| P304 | page(s) | 375-377 | |
| P577 | publication date | 1982-01-01 | |
| P1433 | published in | Human Genetics | Q5937167 |
| P1476 | title | Crossing-over during human spermatogenesis visualized cytologically | |
| P478 | volume | 62 | |