Output details
2 - Public Health, Health Services and Primary Care
Newcastle University
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Output 0 of 0 in the submission
Article title
Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability
Type
D - Journal article
Title of journal
Journal of Medical Genetics
Article number
-
Volume number
48
Issue number
1
First page of article
48
ISSN of journal
1468-6244
Year of publication
2011
Number of additional authors
18
Additional information
The author made a substantial contribution to the organisation of the conduct of the study, to carrying out the study (including acquisition of study data), AND the author helped draft the output and critique the output for important intellectual content.
Interdisciplinary
-
Cross-referral requested
-
Research group
C - Lifecourse, Development and Ageing
Citation count
25
Proposed double-weighted
No
Double-weighted statement
-
Reserve for a double-weighted output
No
Non-English
No
English abstract
-
