About: Children with 4q-syndrome: the parents' perspective

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

scientific article published on 01 January 2007

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в січні 2007 (uk) im Jahr 2007 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en xineru de 2007 (ast) artikull shkencor i botuar më 01 janar 2007 (sq) scientific article published on 01 January 2007 (en)
publication date	wds:Q80822520-68513B7B-B6A6-49B0-8EDF-B03213798C6C
publication date	2007-01-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q80822520-7848765B-C853-4C3C-BC13-E6E0DECEBD20 wds:Q80822520-9D09F7CE-DA1E-4500-A05A-51223B0815DA
author name string	Strehle EM Middlemiss PM
rdfs:label	Children with 4q-syndrome: the parents' perspective (en) Children with 4q-syndrome: the parents' perspective (nl) Children with 4q-syndrome: the parents' perspective (sq)
skos:prefLabel	Children with 4q-syndrome: the parents' perspective (en) Children with 4q-syndrome: the parents' perspective (nl) Children with 4q-syndrome: the parents' perspective (sq)
name	Children with 4q-syndrome: the parents' perspective (en) Children with 4q-syndrome: the parents' perspective (nl) Children with 4q-syndrome: the parents' perspective (sq)
title	wds:Q80822520-8BCE851D-9093-4CBF-ACD4-234F292C7F85
title	Children with 4q-syndrome: the parents' perspective (en)
page(s)	wds:Q80822520-F9225B78-C15B-4866-B3AA-BE6F5C6804AD
page(s)	189-199
instance of	wds:Q80822520-CCC78DF4-A533-4CA5-9802-93509279B9EB
instance of	scholarly article
PubMed ID	wds:Q80822520-A57DF36E-AB9F-44B7-9BBA-5AECBDC01A7F
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/17710871
PubMed ID	17710871
published in	wds:Q80822520-25DF828A-4B29-4A8D-855D-C7A647383BF8
published in	Genetic Counseling
issue	wds:Q80822520-49C58E34-BDCB-45F9-94CA-77E9B96F8B31
volume	wds:Q80822520-ED6B2974-D23E-4A2C-B9DE-4ABD179BC9F5
issue	2
volume	18
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q80822520
is cites work of	4q34.1–q35.2 deletion in a boy with phenotype resembling 22q11.2 deletion syndrome Mutations in C4orf26, encoding a peptide with in vitro hydroxyapatite crystal nucleation and growth activity, cause amelogenesis imperfecta Hand2 function in second heart field progenitors is essential for cardiogenesis. "You have to sit and explain it all, and explain yourself." Mothers' experiences of support services for their offspring with a rare genetic intellectual disability syndrome Parental experiences with behavioural problems in Smith-Magenis syndrome: The need for syndrome-specific competence 4q27 deletion and 7q36.1 microduplication in a patient with multiple malformations and hearing loss: a case report To determine the frequency of subtelomeric abnormalities in children with idiopathic mental retardation
is cites work of	wds:Q91697785-883969C7-F5C1-49C4-81AE-9284288F9256 wds:Q43768715-0C9BEFF6-F741-4A98-8BCC-F305379788B1 wds:Q57207019-449546AC-9D16-4061-996F-F3363E138962 wds:Q90003464-8AF4DDC1-6307-4A15-B2A1-FEDCF8FF5785 wds:Q37037173-1440E417-6BC4-4C2B-85BF-AD2E16339A95 wds:Q34294655-901705A7-5EB0-46A0-BA4E-70BDEC9742A0 wds:Q34574679-EAB0791E-9118-4A18-9A66-22DCEC713227

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