| P2093 | author name string | Tharapel AT | |
| | Wilroy RS | |
| | Martens PR | |
| | Tunca Y | |
| | Gunther WM | |
| | Kadandale JS | |
| P2860 | cites work | Hypomelanosis of Ito: a manifestation of mosaicism or chimerism. | Q33682142 |
| | Chromosome mosaicism in hypomelanosis of Ito. | Q34643118 |
| | Pigmentary abnormalities and mosaicism for chromosomal aberration: association with clinical features similar to hypomelanosis of Ito. | Q34645820 |
| | The gene for incontinentia pigmenti is assigned to Xq28. | Q34677209 |
| | Mosaic loss of 15q11q13 in a patient with hypomelanosis of Ito: is there a role for the P gene? | Q34719918 |
| | Natural history of mosaic trisomy 14 syndrome | Q35561391 |
| | Pigmentary dysplasias, hypomelanosis of Ito, and genetic mosaicism | Q38140614 |
| | Incontinentia pigmenti achromians (hypomelanosis of ITO, MIM 146150): further evidence of localization at Xp11. | Q40821430 |
| | Blaschkolinear malformation syndrome in complex trisomy-7 mosaicism | Q40912476 |
| | Cloning of MITF, the human homolog of the mouse microphthalmia gene and assignment to chromosome 3p14.1-p12.3. | Q48083686 |
| | Hypomelanosis of Ito (incontinentia pigmenti achromians) and mosaicism for a microdeletion of 15q1. | Q52077603 |
| | Trisomy 14 mosaicism with t(14;15)(q11;p11) in offspring of a balanced translocation carrier mother. | Q52265329 |
| P433 | issue | 1 | |
| P304 | page(s) | 39-43 | |
| P577 | publication date | 2000-01-01 | |
| P1433 | published in | Annales de Génétique | Q26842398 |
| P1476 | title | Hypomelanosis of ito and a 'mirror image' whole chromosome duplication resulting in trisomy 14 mosaicism | |
| P478 | volume | 43 | |