Greig cephalopolysyndactyly syndrome: altered phenotype of a microdeletion syndrome due to the presence of a cytogenetic abnormality
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1997.tb02565.x/fullpdf
Reference27 articles.
1. Chromosome 7p-syndrome: craniosynostosis with preservation of region 7p2;Aughton;Am J Med Genet,1991
2. Greig cephalopolysyndactyly: report of 13 affected individuals in three families;Baraitser;Clin Genet,1983
3. Interstitial deletion of the short arm of chromosome 7 without craniosynostosis;Bianci;Clin Genet,1981
4. Six cases of 7p deletion: clinical, cytogenetic and molecular studies;Chotai;Am J Med Genet,1994
5. Partial monosomy with interstitial deletions in two infants with differing congenital abnormalities;Crawford;J Med Genet,1979
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