About: Trisomy of the short stature homeobox-containing gene (SHOX) due to duplication/deletion of the X chomosome: clinical implications on the stature

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About: Trisomy of the short stature homeobox-containing gene (SHOX) due to duplication/deletion of the X chomosome: clinical implications on the stature Goto Sponge NotDistinct Permalink

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scientific article published on 05 August 2010

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в серпні 2010 (uk) im August 2010 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu n'agostu de 2010 (ast) scientific article published on 05 August 2010 (en)
publication date	wds:Q84679285-C5FCD24F-1352-4E68-AFF0-2EC848FF906B
publication date	2010-08-05 00:00:00Z (xsd:dateTime)
author name string	wds:Q84679285-02D66AAE-A6AF-4B78-A657-4F682BB41B1A wds:Q84679285-308F98E5-6871-40E6-9673-D17445603BD1 wds:Q84679285-3A6E90E8-59F1-4046-99D5-47D4146617F8 wds:Q84679285-BF199392-2AA8-4A63-88BC-3C00E3C9B67C wds:Q84679285-D7872BFC-58B6-43CA-A33F-455D07B94BB5
author name string	Juan Jorge Heinrich Adriana Boywitt Graciela del Rey Rodolfo De Bellis Sonia Viviana Bengolea
rdfs:label	Trisomy of the short stature homeobox-containing gene (SHOX) due to duplication/deletion of the X chomosome: clinical implications on the stature (en) Trisomy of the short stature homeobox-containing gene (SHOX) due to duplication/deletion of the X chomosome: clinical implications on the stature (nl)
skos:prefLabel	Trisomy of the short stature homeobox-containing gene (SHOX) due to duplication/deletion of the X chomosome: clinical implications on the stature (en) Trisomy of the short stature homeobox-containing gene (SHOX) due to duplication/deletion of the X chomosome: clinical implications on the stature (nl)
name	Trisomy of the short stature homeobox-containing gene (SHOX) due to duplication/deletion of the X chomosome: clinical implications on the stature (en) Trisomy of the short stature homeobox-containing gene (SHOX) due to duplication/deletion of the X chomosome: clinical implications on the stature (nl)
author	wds:Q84679285-F2F6F325-D580-4ED8-B3F8-735C2EC12BAE
author	Héctor G. Jasper
title	wds:Q84679285-2F358C8A-D7BB-4467-9294-4B23D92FEE83
title	Trisomy of the short stature homeobox-containing gene (SHOX) due to duplication/deletion of the X chomosome: clinical implications on the stature (en)
page(s)	wds:Q84679285-545FA8A6-E75F-4B6F-A1FD-55458EF65239
page(s)	297-304
instance of	wds:Q84679285-4C3FF387-A551-4346-B5B1-68BDB3B2A44B
instance of	scholarly article
PubMed ID	wds:Q84679285-3142A8F0-550C-4EF2-8D9F-2E0EB2179BEB
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/20689243
PubMed ID	20689243
published in	wds:Q84679285-F762C545-3DE4-4B69-B301-4F4625CF352B
published in	Hormone Research in Paediatrics
issue	wds:Q84679285-A0986802-0610-49A9-AE95-788FC2638A3D
volume	wds:Q84679285-2AA85D72-452F-4C88-B00E-F490F1860208
issue	4
volume	74
DOI	wds:Q84679285-7EB4F474-6840-4A6E-86E2-81CF914E3DCB
DOI	http://dx.doi.org/10.1159/000309418
DOI	10.1159/000309418
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q84679285
is cites work of	Rare pseudoautosomal copy-number variations involving SHOX and/or its flanking regions in individuals with and without short stature. A 105 kb interstitial insertion in the Xq27.1 palindrome from pseudoautosomal region PAR1 causes a novel X-linked recessive compound phenotype. Turner syndrome caused by rare complex structural abnormalities involving chromosome X. SHOX Duplication and Tall Stature in a Patient with Xq Deletion and Vascular Disease A case of premature ovarian failure in a 33-year-old woman
is cites work of	wds:Q64958709-6B593D7C-AC4B-4A40-9A58-56AAF792D958 wds:Q41672469-DD96F981-2CE9-45C3-89D3-D12D82634B4F wds:Q64066222-BA70C8E2-BEC0-491D-8FB4-4DF1744C7069 wds:Q52660637-7E7F5E65-A2A2-4957-8B93-99FE34CECF13 wds:Q36602817-2F41A929-B543-4A07-98D8-EB2D0F479126

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