Delineation of a less than 200 kb minimal deleted region for cardiac malformations on chromosome 7p22
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.34041/fullpdf
Reference31 articles.
1. Clinical, chromosomal and enzymatic studies in four cases of rearrangements of chromosome 7;Baeteman;Clin Genet,1985
2. Deletions of the short arm of chromosome 7 without craniosynostosis;Carlo;Clin Genet,1982
3. Identification and characterization of FTSJ2, a novel human nucleolar protein homologous to bacterial ribosomal RNA methyltransferase;Ching;Genomics,2002
4. Six cases of 7p deletion: clinical, cytogenetic, and molecular studies;Chotai;Am J Med Genet,1994
5. Terminal 7p deletion and 1;7 translocation associated with craniosynostosis;Dhadial;Hum Genet,1979
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