Wikidata

(Q50456949)

English

Contiguous gene syndrome due to an interstitial deletion in Xp22.3 in a boy with ichthyosis, chondrodysplasia punctata, mental retardation and ADHD.

scientific article published on 21 May 2007

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Statements

title
Contiguous gene syndrome due to an interstitial deletion in Xp22.3 in a boy with ichthyosis, chondrodysplasia punctata, mental retardation and ADHD (English)
1 reference
stated in
Europe PubMed Central
PubMed ID
17591464
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17591464%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
author name string

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