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A clinical and molecular genetic study of 112 Iranian families with primary microcephaly

โœ Scribed by Darvish, H. (author);Esmaeeli-Nieh, S. (author);Monajemi, G. B. (author);Mohseni, M. (author);Ghasemi-Firouzabadi, S. (author);Abedini, S. S. (author);Bahman, I. (author);Jamali, P. (author);Azimi, S. (author);Mojahedi, F. (author);Dehghan, A. (author);Shafeghati, Y. (author);Jankhah, A. (author);Falah, M. (author);Soltani Banavandi, M. J. (author);Ghani-Kakhi, M. (author);Garshasbi, M. (author);Rakhshani, F. (author);Naghavi, A. (author);Tzschach, A. (author);Neitzel, H. (author);Ropers, H. H. (author);Kuss, A. W. (author);Behjati, F. (author);Kahrizi, K. (author);Najmabadi, Hossein (author)

Book ID
121365587
Publisher
BMJ Publishing Group
Year
2010
Tongue
English
Weight
172 KB
Volume
47
Category
Article
ISSN
0022-2593

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โœ T. T. Warner; L. D. Williams; R. W. H. Walker; F. Flinter; S. A. Robb; S. E. Bun ๐Ÿ“‚ Article ๐Ÿ“… 1995 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 748 KB

Dentatorubropallidoluysian atrophy is a neurodegenerative disorder with characteristic pathology, chiefly described in reports from Japan, and is associated with an unstable CAG trinucleotide repeat in a gene on chromosome 12. We describe four European families, three British and one Maltese, with t