Apparent mosaicism for del(17)(p11.2) ruled out by fluorescence in situ hybridization in a Smith-Magenis syndrome patient - PubMed (original) (raw)
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Apparent mosaicism for del(17)(p11.2) ruled out by fluorescence in situ hybridization in a Smith-Magenis syndrome patient
R C Juyal et al. Am J Med Genet. 1995.
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- Mosaicism for deletion 17p11.2 in a boy with the Smith-Magenis syndrome.
Finucane BM, Kurtz MB, Babu VR, Scott CI Jr. Finucane BM, et al. Am J Med Genet. 1993 Feb 15;45(4):447-9. doi: 10.1002/ajmg.1320450410. Am J Med Genet. 1993. PMID: 8465848
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