Pigmentary abnormalities and mosaicism for chromosomal aberration: association with clinical features similar to hypomelanosis of Ito.

scientific article

Pigmentary abnormalities and mosaicism for chromosomal aberration: association with clinical features similar to hypomelanosis of Ito. is …
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scholarly articleQ13442814

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P356DOI10.1016/S0022-3476(05)81606-3
P8608Fatcat IDrelease_nqbu65nj3fgmjouhx25ou5s6gm
P698PubMed publication ID2319405

P2093author name stringBradley CM
Donlan M
Pagon RA
Sybert VP
P2860cites workThe characteristic physiognomy and tissue specific karyotype distribution in the Pallister-Killian syndromeQ28235658
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 karyotypesQ34298019
Hypomelanosis of Ito: a neurocutaneous syndromeQ35115290
The lines of Blaschko: a review and reconsideration: Observations of the cause of certain unusual linear conditions of the skinQ40611138
Aberrant melanoblast migration associated with trisomy 18 mosaicismQ41885083
Hypomelanosis of Ito associated with benign tumors and chromosomal abnormalities: a neurocutaneous syndromeQ48551659
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 findingsQ53842347
Incontinentia pigmenti achromiansQ66940354
Incontinentia pigmenti achromians. Multiple cases within a familyQ67291160
Hypomelanosis of Ito: spectrum of the diseaseQ69640837
Proceedings: Unilateral systematized hypochromic nevusQ69739720
Diploid/triploid mixoploidy and hypomelanosis of ItoQ69882445
Trisomy 22 mosaicism syndrome and Ullrich-Turner stigmataQ70024579
Hypomelanosis of Ito: association with a chromosomal abnormalityQ70077535
P433issue4
P407language of work or nameEnglishQ1860
P304page(s)581-586
P577publication date1990-04-01
P1433published inThe Journal of PediatricsQ7743611
P1476titlePigmentary abnormalities and mosaicism for chromosomal aberration: association with clinical features similar to hypomelanosis of Ito.
P478volume116