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AJMG.1320360312
AJMG.1320360312
http://dx.doi.org/10.1002/AJMG.1320360312
Holoprosencephaly in an infant with a minute deletion of chromosome 21(q22.3).
P356
Q48939764-DA1B70FD-AE8A-449D-BE61-C4A28EC78729
P356
AJMG.1320360312
http://dx.doi.org/10.1002/AJMG.1320360312