Joubert syndrome: a patient with a de novo t(2;22)(q13;q11.1)

Hatchwell, E., Tommerup, N., Kristoffersson, U., Stanyon, R., Kantarci, S. (November 2003) Joubert syndrome: a patient with a de novo t(2;22)(q13;q11.1). American Journal of Human Genetics, 73 (5). p. 566. ISSN 0002-9297

URL: http://www.ashg.org/genetics/abstracts/abs03/f2334...
Item Type: Paper
Additional Information: Meeting Abstract
Subjects: bioinformatics > genomics and proteomics > genetics & nucleic acid processing
bioinformatics > genomics and proteomics
bioinformatics > genomics and proteomics > genetics & nucleic acid processing > genomes
CSHL Authors:
Communities: CSHL labs > Hatchwell lab
Depositing User: Matt Covey
Date: November 2003
Date Deposited: 01 Jul 2013 20:33
Last Modified: 01 Jul 2013 20:33
URI: http://repository.cshl.edu/id/eprint/27854

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