(Q52087713)

English

[Patterns on the skin. New aspects of their embryologic and genetic causes].

scientific article published in October 2004

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Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/15351866

1 reference

Europe PubMed Central

[Patterns on the skin. New aspects of their embryologic and genetic causes]. (English)

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/15351866

author name string

R Happle

1

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/15351866

language of work or name

0 references

publication date

1 October 2004

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/15351866

Die Dermatologie

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/15351866

55

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/15351866

10

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/15351866

960-1, 964-8

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/15351866

https://scigraph.springernature.com/pub.10.1007/s00105-004-0796-2

0 references

Dohi Memorial Lecture. New aspects of cutaneous mosaicism

1 reference

https://api.crossref.org/works/10.1007%2FS00105-004-0796-2

21 January 2018

Controlling elements and the gene

1 reference

https://api.crossref.org/works/10.1007%2FS00105-004-0796-2

21 January 2018

LINE-1 elements and X chromosome inactivation: a function for "junk" DNA?

1 reference

https://pubmed.ncbi.nlm.nih.gov/15351866

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phacomatosis pigmentokeratotica: a patient with the rare melanocytic-epidermal twin nevus syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/15351866

12 December 2020

based on heuristic

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[Segmental type 2 manifestation of autosome dominant skin diseases. Development of a new formal genetic concept]

1 reference

https://pubmed.ncbi.nlm.nih.gov/15351866

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular evidence for a relationship between LINE-1 elements and X chromosome inactivation: the Lyon repeat hypothesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/15351866

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The marks, mechanisms and memory of epigenetic states in mammals

1 reference

https://pubmed.ncbi.nlm.nih.gov/15351866

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Speckled lentiginous nevus syndrome: delineation of a new distinct neurocutaneous phenotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/15351866

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-chromosome inactivation: a repeat hypothesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/15351866

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recombinagenic activity of four compounds in the standard and high bioactivation crosses of Drosophila melanogaster in the wing spot test

1 reference

https://pubmed.ncbi.nlm.nih.gov/15351866

12 December 2020

based on heuristic

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Metastable epialleles in mammals

1 reference

https://pubmed.ncbi.nlm.nih.gov/15351866

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High concentrations of long interspersed nuclear element sequence distinguish monoallelically expressed genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/15351866

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The impact of L1 retrotransposons on the human genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/15351866

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transposable genetic elements as agents of gene instability and chromosomal rearrangements

1 reference

https://pubmed.ncbi.nlm.nih.gov/15351866

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Revertant mosaicism in epidermolysis bullosa caused by mitotic gene conversion

1 reference

https://pubmed.ncbi.nlm.nih.gov/15351866

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Phylloid hypomelanosis and mosaic trisomy 13: a new etiologically defined neurocutaneous syndrome]

1 reference

https://pubmed.ncbi.nlm.nih.gov/15351866

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the NSDHL gene, encoding a 3beta-hydroxysteroid dehydrogenase, cause CHILD syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/15351866

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pigmentary mosaicism of the hyperpigmented type in two half-brothers.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15351866

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00105-004-0796-2

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/15351866

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/15351866

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