DOI:
10.1055/s-00000034
Klinische Pädiatrie
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References
Prasad C, Prasad AN, Chodirker BN, Lee C, Dawson AK, Jocelyn LJ, Chudley AE.
Genetic evaluation of pervasive developmental disorders: the terminal 22q13 deletion syndrome may represent a recognizable phenotype.
Clin Genet 2000; 57: 103-109
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