| P2093 | author name string | I K Temple | |
| | A M Fisher | |
| | C J Law | |
| P2860 | cites work | Autosomal dominant iridogoniodysgenesis anomaly maps to 6p25 | Q24675534 |
| | Autosomal dominant Axenfeld-Rieger anomaly maps to 6p25 | Q24678473 |
| | Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4. | Q33680461 |
| | Partial deletion of chromosome 6p: delineation of the syndrome | Q37773731 |
| | A patient with an interstitial deletion of the short arm of chromosome 6 | Q39710096 |
| | Terminal deletion of 6p: report of a new case. | Q40502744 |
| | Two rare cases of 6p partial deletion. | Q41931827 |
| | A detailed investigation of two cases exhibiting characteristics of the 6p deletion syndrome. | Q52007413 |
| | Terminal deletion 6p23: a case report | Q68635194 |
| | Distal deletion of the short arm of chromosome 6 | Q68721251 |
| | Tandem Y/6 translocation with partial deletion 6 (p23----pter) | Q69747946 |
| | A complete set of human telomeric probes and their clinical application. National Institutes of Health and Institute of Molecular Medicine collaboration | Q71473129 |
| | Evidence of a locus for orofacial clefting on human chromosome 6p24 and STS content map of the region | Q72144569 |
| | Clinical evidence for localisation of HLA proximal of chromosome 6p22 | Q72547077 |
| P433 | issue | 8 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 685-689 | |
| P577 | publication date | 1998-08-01 | |
| P1433 | published in | Journal of Medical Genetics | Q14640281 |
| P1476 | title | Distal 6p deletion syndrome: a report of a case with anterior chamber eye anomaly and review of published reports | |
| P478 | volume | 35 | |