DOI:
10.1055/s-00000034
Klinische Pädiatrie
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References
Cassidy SB, Forsythe M, Heeger S, Nicholls RD, Schork N, Benn P, Schwarzt S.
Comparison of phenotype between patients with Prader-Willi syndrome due to deletion 15q and uniparental disomy 15.
Am J Med Genet 1997a;; 68: 433-440
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