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515520
515520
http://dx.doi.org/10.1086/515520
Chromosome 1p36 deletions: the clinical phenotype and molecular characterization of a common newly delineated syndrome
P356
Q34743172-249C0FA8-6EF0-4085-A412-87BA262E9018
P356
515520
http://dx.doi.org/10.1086/515520