Review
doi: 10.1136/jmg.26.8.528.
De novo terminal deletion 7p22.1--pter in a child without craniosynostosis
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- PMID: 2671374
- PMCID: PMC1015678
- DOI: 10.1136/jmg.26.8.528
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Review
De novo terminal deletion 7p22.1--pter in a child without craniosynostosis
J Med Genet.
1989 Aug.
Abstract
A patient with a de novo terminal deletion of the short arm of chromosome 7 (p22.1--pter) is described. Facial dysmorphism, a congenital heart defect, and genital hypoplasia were evident. There were no signs of craniosynostosis. Our observation confirms that deletion of 7p22 is not necessarily associated with craniosynostosis.
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