Frequent intragenic polymorphism in the 3‘ untranslated region of the lissencephaly gene 1 (LIS-1)
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1996.tb02728.x/fullpdf
Reference6 articles.
1. Microsatellite analysis of loss of heterozygosity on chromosomes 9q, 11p and 17p in medulloblastomas;Albrecht;Neuropathol Appl Neurobiol,1994
2. Analysis of VNTR locus D1S80 by PCR followed by high-resolution PAGE;Budowle;Am J Hum Genet,1991
3. Lissencephaly. A human brain malformation associated with deletion of the LIS1 gene located at chromosome 17p13;Dobyns;JAMA,1993
4. Molecular analysis of the lissencephaly gene 1 (LIS-1) in medulloblastomas;Koch;Neuropathol Appl Neurobiol,1996
5. Isolation of Miller-Dieker lissencephaly gene containing G protein β-subunit-like repeats;Reiner;Nature,1993
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Human cytomegalovirus infection is associated with increased expression of the lissencephaly gene PAFAH1B1 encoding LIS1 in neural stem cells and congenitally infected brains;The Journal of Pathology;2021-03-24
2. Deletion of 17p13 and LIS1 Gene Mutation in Isolated Lissencephaly Sequence;Pediatric Neurology;2006-07
3. Clinical and molecular basis of classical lissencephaly: Mutations in theLIS1 gene (PAFAH1B1);Human Mutation;2001-12-12
4. Analysis of the max-binding protein MNT in human medulloblastomas;International Journal of Cancer;1999-09-09
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