Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader–Willi syndrome
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J. Rosenfeld | L. Shaffer | B. Ballif | B. Bejjani | R. Person | T. Sahoo | S. Alliman | A. Lamb | R. Thompson | A. Duker | E. Bawle | S. Mahadevan | R. Traylor | Angela L. Duker | Sarah Alliman | Ryan N. Traylor