(Q34286696)

English

The CHILD syndrome. Congenital hemidysplasia with ichthyosiform erythroderma and limb defects

scientific article

In more languages

default for all languages

No label defined

No description defined

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

The CHILD syndrome. Congenital hemidysplasia with ichthyosiform erythroderma and limb defects (English)

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

congenital disorder

0 references

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

author name string

Happle R

1

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Koch H

2

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Lenz W

3

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

publication date

1 June 1980

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

European Journal of Pediatrics

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

134

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

27-33

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Knowledge of Solomon's epidermal nevus syndrome (author's transl)

1 reference

https://pubmed.ncbi.nlm.nih.gov/7408908

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Syndrome of unilateral ectromelia, psoriasis and central nervous system anomalies

1 reference

https://pubmed.ncbi.nlm.nih.gov/7408908

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

UNILATERAL ICHTHYOSIFORM ERYTHRODERMA

1 reference

https://pubmed.ncbi.nlm.nih.gov/7408908

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Unilateral limb and skin deformities with congenital heart disease in two siblings: A lethal syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/7408908

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[On the Schimmelpenning-Feuerstein-Mims-syndrome (Organoid Nevus-Phakomatosis) (author's transl)]

1 reference

https://pubmed.ncbi.nlm.nih.gov/7408908

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linear ichthyosis associated with skeletal abnormalities.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7408908

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Q--congenital hemidysplasia with ichthyosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/7408908

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

1 reference

https://pubmed.ncbi.nlm.nih.gov/7408908

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital unilateral ichthyosiform erythroderma

1 reference

https://pubmed.ncbi.nlm.nih.gov/7408908

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital unilateral ichthyosis in a newborn

1 reference

https://pubmed.ncbi.nlm.nih.gov/7408908

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The epidermal nevus syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/7408908

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inflammatory linear verrucous epidermal nevus. Association with epidermal nevus syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/7408908

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked dominant chondrodysplasia punctata. Review of literature and report of a case

1 reference

https://pubmed.ncbi.nlm.nih.gov/7408908

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inflammatory variable epidermal naevus (atypical I.L.V.E.N.? A new entity?) (author's transl)

1 reference

https://pubmed.ncbi.nlm.nih.gov/7408908

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00442399

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q34286696&oldid=2196463636"