Clinical report: inherited deletion of chromosome 12q21.31q21.32 associated with a distinct phenotype and intellectual disability. Issue 4 (October 2015)

Record Type:
Journal Article
Title:
Clinical report: inherited deletion of chromosome 12q21.31q21.32 associated with a distinct phenotype and intellectual disability. Issue 4 (October 2015)
Main Title:
Clinical report
Authors:
Akilapa, Rhoda S.
Smith, Kath
Balasubramanian, Meena
Abstract:
Is Part Of:
Clinical dysmorphology. Volume 24:Issue 4(2015:Oct.)
Journal:
Clinical dysmorphology
Issue:
Volume 24:Issue 4(2015:Oct.)
Issue Display:
Volume 24, Issue 4 (2015)
Year:
2015
Volume:
24
Issue:
4
Issue Sort Value:
2015-0024-0004-0000
Page Start:
Page End:
Publication Date:
2015-10
Subjects:
Abnormalities, Human -- Periodicals
Genetic disorders -- Periodicals
Abnormalities -- periodicals
Abnormalities, Human
Periodicals
616.042
Journal URLs:
http://gateway.ovid.com/ovidweb.cgi?T=JS&MODE=ovid&NEWS=n&PAGE=toc&D=ovft&AN=00019605-000000000-00000 ↗
http://journals.lww.com/clindysmorphol/pages/default.aspx ↗
http://journals.lww.com/pages/default.aspx ↗
http://firstsearch.oclc.org ↗
DOI:
10.1097/MCD.0000000000000096 ↗
Languages:
English
ISSNs:
0962-8827
Deposit Type:
Legaldeposit
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:
British Library DSC - 3286.273700
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store
Ingest File:
5174.xml