The Smith-Magenis syndrome [del(17)p11.2]: Clinical review and molecular advances

This publication has 75 references indexed in Scilit:

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• Case reports of autism with interstitial deletion of chromosome 17 (p11.2 p11.2) and monosomy of chromosome 5 (5pter → 5p 15.3)
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• In humans all U3 genes map to chromosome 17p12→p11, but in mouse the U3A and U3B genes are located on different chromosomes
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