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Genetic regulation of cerebellar development.
Wang VY, Zoghbi HY. Wang VY, et al. Among authors: zoghbi hy. Nat Rev Neurosci. 2001 Jul;2(7):484-91. doi: 10.1038/35081558. Nat Rev Neurosci. 2001. PMID: 11433373 Review. No abstract available.
Genetic aspects of Rett syndrome.
Zoghbi H. Zoghbi H. J Child Neurol. 1988;3 Suppl:S76-8. doi: 10.1177/0883073888003001s15. J Child Neurol. 1988. PMID: 3058791 Review.
Spinocerebellar ataxia type 1.
Zoghbi HY. Zoghbi HY. Clin Neurosci. 1995;3(1):5-11. Clin Neurosci. 1995. PMID: 7614095 Review.
A high resolution deletion map of human chromosome Xp22.
Schaefer L, Ferrero GB, Grillo A, Bassi MT, Roth EJ, Wapenaar MC, van Ommen GJ, Mohandas TK, Rocchi M, Zoghbi HY, Ballabio A. Schaefer L, et al. Among authors: zoghbi hy. Nat Genet. 1993 Jul;4(3):272-9. doi: 10.1038/ng0793-272. Nat Genet. 1993. PMID: 8358436
Purkinje cell expression of a mutant allele of SCA1 in transgenic mice leads to disparate effects on motor behaviors, followed by a progressive cerebellar dysfunction and histological alterations.
Clark HB, Burright EN, Yunis WS, Larson S, Wilcox C, Hartman B, Matilla A, Zoghbi HY, Orr HT. Clark HB, et al. Among authors: zoghbi hy. J Neurosci. 1997 Oct 1;17(19):7385-95. doi: 10.1523/JNEUROSCI.17-19-07385.1997. J Neurosci. 1997. PMID: 9295384 Free PMC article.
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