Comparison of TFII-I gene family members deleted in Williams-Beuren syndrome
Author:
Publisher
Wiley
Subject
Molecular Biology,Biochemistry
Reference69 articles.
1. Basic local alignment search tool;Altschul;J. Mol. Biol.,1990
2. High level of unequal meiotic crossovers at the origin of the 22q11.2 and 7q11.23 deletions;Baumer;Hum. Mol. Genet.,1998
3. Genomic organization of the genes Gtf2ird1, Gtf2i and Ncf1 at the mouse chromosome 5 region syntenic to the human chromosome 7q11.23 Williams syndrome critical region;Bayarsaihan;Genomics,2002
4. The neurocognitive profile of Williams syndrome: A complex pattern of strengths and weaknesses;Bellugi;J. Cogn. Neurosci.,2000
5. The protein Id: A negative regulator of helix-loop-helix DNA binding proteins;Benezra;Cell,1990
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