(Q41864756)

English

"Cutis tricolor": congenital hyper- and hypopigmented macules associated with a sporadic multisystem birth defect: an unusual example of twin spotting?

scientific article published on August 1997

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

"Cutis tricolor": congenital hyper- and hypopigmented macules associated with a sporadic multisystem birth defect: an unusual example of twin spotting? (English)

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

congenital disorder

0 references

author name string

Happle R

1

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

Barbi G

2

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

Eckert D

3

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

Kennerknecht I

4

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

language of work or name

0 references

publication date

1 August 1997

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

Journal of Medical Genetics

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

34

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

8

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

676-678

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

Mosaicism in human skin. Understanding the patterns and mechanisms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051032

5 June 2018

Bloom syndrome: a mendelian prototype of somatic mutational disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051032

5 June 2018

Asymmetry and skin pigmentary anomalies in chromosome mosaicism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051032

5 June 2018

Hypomelanosis of Ito: a manifestation of mosaicism or chimerism.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051032

5 June 2018

Association of pigmentary anomalies with chromosomal and genetic mosaicism and chimerism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051032

5 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051032

5 June 2018

Hypothesis: vascular twin naevi and somatic recombination in man.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051032

5 June 2018

Phacomatosis pigmentokeratotica: a melanocytic-epidermal twin nevus syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051032

16 June 2018

Somatic mutation and recombination test in Drosophila melanogaster.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051032

18 August 2018

Incontinentia pigmenti achromians (Ito)

1 reference

https://pubmed.ncbi.nlm.nih.gov/9279762

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pigmentary dysplasias and chromosomal mosaicism: report of 9 cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/9279762

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JMG.34.8.676

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

ResearchGate publication ID

0 references

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