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(Reference retrieved automatically from Google Scholar through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Deletions encompassing 1q41q42. 1 and clinical features of autosomal dominant Robinow syndrome

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Author(s):
Mazzeu‚ JF ; Vianna-Morgante‚ AM ; Krepischi‚ ACV ; Oudakker‚ A. ; Rosenberg‚ C. ; Szuhai‚ K. ; McGill‚ J. ; MacCraughan‚ J. ; Van Bokhoven‚ H. ; Brunner‚ HG
Total Authors: 10
Document type: Journal article
Source: Clinical Genetics; v. 77, n. 4, p. 404-407, 2010.
FAPESP's process: 98/14254-2 - The Human Genome Research Center
Grantee:Mayana Zatz
Support type: Research Grants - Research, Innovation and Dissemination Centers - RIDC