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  Joubert syndrome: genotyping a Northern European patient cohort

Kroes, H. Y., Monroe, G. R., van der Zwaag, B., Duran, K. J., De Kovel, C. G. F., van Roosmalen, M. J., et al. (2016). Joubert syndrome: genotyping a Northern European patient cohort. European Journal of Human Genetics, 24(2), 214-20. doi:10.1038/ejhg.2015.84.

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 Creators:
Kroes, H. Y., Author
Monroe, G. R., Author
van der Zwaag, B., Author
Duran, K. J., Author
De Kovel, Carolien G. F.1, Author           
van Roosmalen, M. J., Author
Harakalova, M., Author
Nijman, I. J., Author
Kloosterman, W. P., Author
Giles, R. H., Author
Knoers, N. V., Author
van Haaften, G., Author
Affiliations:
1University Medical Center Utrecht, ou_persistent22              

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Language(s): eng - English
 Dates: 2016
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1038/ejhg.2015.84
 Degree: -

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Title: European Journal of Human Genetics
Source Genre: Journal
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Affiliations:
Publ. Info: Basel : Karger
Pages: - Volume / Issue: 24 (2) Sequence Number: - Start / End Page: 214 - 20 Identifier: ISSN: 1018-4813
CoNE: https://pure.mpg.de/cone/journals/resource/954925585277_2