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Deletion mapping: Further evidence for the location of acid phosphatase (ACP1) within 2p23
Authors:B. S. Emanuel  E. H. Zackai  D. C. Van Dyke  D. M. Swallow  F. H. Allen  W. J. Mellman
Abstract:
Keywords:Multiple congenital anomaly (MCA) syndrome  hypotonia  failure to thrive  delayed psychomotor development  microcephaly  mental retardation  deletion 2p23→  ter  erythrocyte acid phosphatase (ACP1)  ACP1 alleles B, A, deletion mapping ACP1 in 2p23
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