scholarly article | Q13442814 |
P356 | DOI | 10.1016/S0022-3476(05)81606-3 |
P8608 | Fatcat ID | release_nqbu65nj3fgmjouhx25ou5s6gm |
P698 | PubMed publication ID | 2319405 |
P2093 | author name string | Bradley CM | |
Donlan M | |||
Pagon RA | |||
Sybert VP | |||
P2860 | cites work | The characteristic physiognomy and tissue specific karyotype distribution in the Pallister-Killian syndrome | Q28235658 |
Interstitial deletion of the long arm of chromosome 2 with normal levels of isocitrate dehydrogenase. | Q33592816 | ||
Hypomelanosis of Ito: a manifestation of mosaicism or chimerism. | Q33682142 | ||
A true hermaphrodite dispermic chimera with 46,XX and 46,XY karyotypes | Q34298019 | ||
Hypomelanosis of Ito: a neurocutaneous syndrome | Q35115290 | ||
The lines of Blaschko: a review and reconsideration: Observations of the cause of certain unusual linear conditions of the skin | Q40611138 | ||
Aberrant melanoblast migration associated with trisomy 18 mosaicism | Q41885083 | ||
Hypomelanosis of Ito associated with benign tumors and chromosomal abnormalities: a neurocutaneous syndrome | Q48551659 | ||
Hypomelanosis of Ito (incontinentia pigmenti achromians) and mosaicism for a microdeletion of 15q1. | Q52077603 | ||
Trisomy 18/trisomy 13 mosaicism in an adult with profound mental retardation and multiple malformations. | Q52094711 | ||
Trisomy 14 mosaicism with t(14;15)(q11;p11) in offspring of a balanced translocation carrier mother. | Q52265329 | ||
A boy with ring chromosome 15 derived from a t(15q;15q) robertsonian translocation in the mother: Cytogenetic and biochemical findings | Q53842347 | ||
Incontinentia pigmenti achromians | Q66940354 | ||
Incontinentia pigmenti achromians. Multiple cases within a family | Q67291160 | ||
Hypomelanosis of Ito: spectrum of the disease | Q69640837 | ||
Proceedings: Unilateral systematized hypochromic nevus | Q69739720 | ||
Diploid/triploid mixoploidy and hypomelanosis of Ito | Q69882445 | ||
Trisomy 22 mosaicism syndrome and Ullrich-Turner stigmata | Q70024579 | ||
Hypomelanosis of Ito: association with a chromosomal abnormality | Q70077535 | ||
P433 | issue | 4 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 581-586 | |
P577 | publication date | 1990-04-01 | |
P1433 | published in | The Journal of Pediatrics | Q7743611 |
P1476 | title | Pigmentary abnormalities and mosaicism for chromosomal aberration: association with clinical features similar to hypomelanosis of Ito. | |
P478 | volume | 116 |