SNP genotyping to screen for a common deletion in CHARGE Syndrome
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* Corresponding author: John W Belmont jbelmont@bcm.tmc.edu
BMC Medical Genetics 2005, 6:8 doi:10.1186/1471-2350-6-8
Pre-publication versions of this article and reviewers' reports
| Original Submission - Version 1 | Manuscript | 16 Jul 2004 | |
| Resubmission - Version 2 | Manuscript | 29 Jul 2004 | |
| Reviewer's Report | Derek Gordon | 30 Aug 2004 | |
| Reviewer's Report | Brian Schutte | 07 Oct 2004 | |
| Resubmission - Version 3 | Manuscript | Author's comment | 24 Nov 2004 |
| Reviewer's Report | Brian Schutte | 16 Dec 2004 | |
| Published | 14 Feb 2005 |