Output details
1 - Clinical Medicine
University of Cambridge
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Output 0 of 0 in the submission
Output title
Complex inheritance of a rare microdeletion and low frequency regulatory SNP cause TAR syndrome. A model for other microdeletion disorders
Type
E - Conference contribution
DOI
-
Name of conference/published proceedings
JOURNAL OF MEDICAL GENETICS
Volume number
49
Issue number
-
First page of article
S38
ISSN of proceedings
0022-2593
Year of publication
2012
URL
-
Number of additional authors
9
Additional information
-
Interdisciplinary
-
Cross-referral requested
-
Research group
None
Citation count
44
Proposed double-weighted
No
Double-weighted statement
-
Reserve for a double-weighted output
No
Non-English
No
English abstract
-