About: First reported case of interstitial 15 q15.3-q21.3 deletion diagnosed prenatally and characterized with array CGH in a fetus with an isolated short femur

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About: First reported case of interstitial 15 q15.3-q21.3 deletion diagnosed prenatally and characterized with array CGH in a fetus with an isolated short femur Goto Sponge NotDistinct Permalink

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scientific article published on 02 February 2012

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в березні 2012 (uk) im Februar 2012 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en febreru de 2012 (ast) scientific article published on 02 February 2012 (en)
publication date	wds:Q56321921-2BEFEF97-1E2F-4A14-91BB-36AE71BC721D
publication date	2012-02-02 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q56321921-B8C879B6-76C0-424F-9780-F47A018BA53E
language of work or name	English
cites work	wds:Q56321921-000A06A2-E9B3-4425-B980-658A7C3FBA89 wds:Q56321921-1AC756EC-5FF8-4C3C-AB24-5E47FE6CB657 wds:Q56321921-BFE4F959-F4A9-4035-97ED-0361400E0DE5 wds:Q56321921-F09FDECE-7CF8-4C44-8506-D5469505740F
cites work	Craniosynostosis in a patient with a de novo 15q15-q22 deletion Coarctation of the aorta and mild to moderate developmental delay in a child with a de novo deletion of chromosome 15(q21.1q22.2) Craniosynostosis and congenital heart anomalies associated with a maternal deletion of 15q15-22.1 Craniosynostosis in an infant with an interstitial deletion of 15q [46,XY,del(15)(q15q22.1)]
author name string	wds:Q56321921-4959EA8B-8997-47E1-9CF5-575306ADB5A0 wds:Q56321921-55D199F0-A02A-42E7-B76B-C75FA28087BA wds:Q56321921-6F2475A5-A127-4174-B610-B8C214E96405 wds:Q56321921-D0CD518C-59EC-4CCF-B991-1DE62D19BD4B wds:Q56321921-DC8D9201-6DDF-40D9-9F51-6A1612263ED3 wds:Q56321921-E51E6970-F0F3-4C9A-9D99-C3981B138925 wds:Q56321921-FAB3CF39-ED7B-49EA-B580-1507C42CA607
author name string	Vassilis Tsatsaris Laurence Cuisset Johanna Corcos Fatma Abdelhedi Julia Tantau Aziza Lebbar Dominique Le Tessier
rdfs:label	First reported case of interstitial 15 q15.3-q21.3 deletion diagnosed prenatally and characterized with array CGH in a fetus with an isolated short femur (en) First reported case of interstitial 15 q15.3-q21.3 deletion diagnosed prenatally and characterized with array CGH in a fetus with an isolated short femur (nl)
skos:prefLabel	First reported case of interstitial 15 q15.3-q21.3 deletion diagnosed prenatally and characterized with array CGH in a fetus with an isolated short femur (en) First reported case of interstitial 15 q15.3-q21.3 deletion diagnosed prenatally and characterized with array CGH in a fetus with an isolated short femur (nl)
name	First reported case of interstitial 15 q15.3-q21.3 deletion diagnosed prenatally and characterized with array CGH in a fetus with an isolated short femur (en) First reported case of interstitial 15 q15.3-q21.3 deletion diagnosed prenatally and characterized with array CGH in a fetus with an isolated short femur (nl)
author	wds:Q56321921-52D5A28E-C6FF-4FF1-BF34-F9C5E5F2A5BB
author	Jean-Michel Dupont
title	wds:Q56321921-A61C34B5-B8A7-483D-8CF5-8513D8E8BE17
title	First reported case of interstitial 15 q15.3-q21.3 deletion diagnosed prenatally and characterized with array CGH in a fetus with an isolated short femur (en)
page(s)	wds:Q56321921-42FF9BCB-2F57-4A5F-BF0E-20ADB7EFE673
page(s)	617-621
instance of	wds:Q56321921-0FF04627-C260-45E3-B982-A2A73C365204
instance of	scholarly article
PubMed ID	wds:Q56321921-C699AED1-B92C-41C0-AC61-A61B9B45E9B9
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/22302515
PubMed ID	22302515
published in	wds:Q56321921-D65A04E9-ED67-48DA-AACF-1867CBBCF922
published in	American Journal of Medical Genetics
issue	wds:Q56321921-D67C8A8B-6918-4C97-A167-C188454CCA5C
volume	wds:Q56321921-AC59DB60-7038-44A1-8C6A-6937404152FC
issue	3
volume	158A
DOI	wds:Q56321921-8894855B-A484-48AF-B243-4F2AAAB06FF5
DOI	http://dx.doi.org/10.1002/AJMG.A.34416
DOI	10.1002/AJMG.A.34416
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q56321921

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