(Q34645820)

3 August 2017

title

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

1 reference

3 August 2017

Sybert VP

1

1 reference

3 August 2017

Pagon RA

series ordinal

2

1 reference

3 August 2017

Donlan M

series ordinal

3

1 reference

3 August 2017

Bradley CM

series ordinal

4

1 reference

3 August 2017

language of work or name

English

0 references

publication date

1 April 1990

1 reference

The Journal of Pediatrics

3 August 2017

published in

1 reference

3 August 2017

volume

116

1 reference

3 August 2017

issue

4

1 reference

3 August 2017

page(s)

581-586

1 reference

Incontinentia pigmenti achromians. Multiple cases within a family

3 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2981606-3

Proceedings: Unilateral systematized hypochromic nevus

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2981606-3

Hypomelanosis of Ito: a neurocutaneous syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2981606-3

Incontinentia pigmenti achromians

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2981606-3

Interstitial deletion of the long arm of chromosome 2 with normal levels of isocitrate dehydrogenase.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2981606-3

Diploid/triploid mixoploidy and hypomelanosis of Ito

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2981606-3

Hypomelanosis of Ito: a manifestation of mosaicism or chimerism.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2981606-3

A true hermaphrodite dispermic chimera with 46,XX and 46,XY karyotypes

7 January 2021

2 references

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2981606-3

7 January 2021

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2981606-3

7 January 2021

inferred from DOI database lookup

Hypomelanosis of Ito (incontinentia pigmenti achromians) and mosaicism for a microdeletion of 15q1.

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2981606-3

Trisomy 18/trisomy 13 mosaicism in an adult with profound mental retardation and multiple malformations.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2981606-3

Trisomy 22 mosaicism syndrome and Ullrich-Turner stigmata

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2981606-3

The characteristic physiognomy and tissue specific karyotype distribution in the Pallister-Killian syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2981606-3

Hypomelanosis of Ito: association with a chromosomal abnormality

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2981606-3

A boy with ring chromosome 15 derived from a t(15q;15q) robertsonian translocation in the mother: Cytogenetic and biochemical findings

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2981606-3

Trisomy 14 mosaicism with t(14;15)(q11;p11) in offspring of a balanced translocation carrier mother.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2981606-3

Hypomelanosis of Ito: spectrum of the disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2981606-3

The lines of Blaschko: a review and reconsideration: Observations of the cause of certain unusual linear conditions of the skin

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2981606-3

Aberrant melanoblast migration associated with trisomy 18 mosaicism

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2981606-3

7 January 2021

inferred from DOI database lookup

Hypomelanosis of Ito associated with benign tumors and chromosomal abnormalities: a neurocutaneous syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2981606-3

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1016/S0022-3476(05)81606-3

1 reference

release_nqbu65nj3fgmjouhx25ou5s6gm

3 August 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/nqbu65nj3fgmjouhx25ou5s6gm

24 November 2022

mapped directly with Wikidata item

1 reference