Publikationen
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Oiglane-Shlik, E; Zordania, R; Varendi, H et al.
The neonatal phenotype of Prader-Willi syndrome.Am J Med Genet. Bd. 140. H. 11. 2006 S. 1241-4
Bartsch, O; Ergun, MA; Balci, S et al.
Two complementary recombinant chromosomes 5 in a healthy woman.Cytogenet Genome Res. Bd. 114. H. 2. 2006 S. 178-82