| P2093 | author name string | C Stoll | |
| | A Pennerath | |
| | C Lausecker | |
| P2860 | cites work | Translocation 4p-- syndrome: a general review | Q34162821 |
| | Deficiency on the short arms of a chromosome No. 4 | Q34241073 |
| | Deletion of short arms of chromosome 4?5 in a child with defects of midline fusion | Q34241369 |
| | Polymporphism of human C-band heterochromatin. II. Family studies with suggestive evidence for somatic crossing over | Q35570512 |
| | Ophthalmic Features of Chromosome Deletion 4p-(Wolf-Hirschhorn Syndrome) | Q39643339 |
| | 4p- Phenotype in an Infant With t(4p-;19p or q + )mat Translocation | Q66918107 |
| | Human Q and C chromosomal variations: distribution and incidence | Q66956192 |
| P433 | issue | 3 | |
| P304 | page(s) | 413-415 | |
| P577 | publication date | 1981-01-01 | |
| P1433 | published in | Human Genetics | Q5937167 |
| P1476 | title | 4p- syndrome in a girl with translocation t(1;4)(q11;p16)mat | |
| P478 | volume | 56 | |