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Genome-wide analysis of single-nucleotide polymorphisms in human expressed sequences

✍ Scribed by Irizarry, Kris; Kustanovich, Vlad; Li, Cheng; Brown, Nik; Nelson, Stanley; Wong, Wing; Lee, Christopher J.

Book ID: 109829102
Publisher: Nature Publishing Group
Year: 2000
Tongue: English
Weight: 362 KB
Volume: 26
Category: Article
ISSN: 1061-4036
DOI: 10.1038/79981

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## Abstract Ollier disease and Maffucci syndrome are rare, nonhereditary skeletal disorders characterized by the presence of multiple enchondromas with (Maffucci) or without (Ollier) co‐existing multiple hemangiomas of soft tissue. Enchondromas can progress toward central chondrosarcomas. __PTH1R__