Z Geburtshilfe Neonatol
 2005
DOI: 10.1055/s-2005-871350
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Diagnostik des congenitalen zentralen Hypoventilationssyndroms (CCHS) durch Mutationsanalyse im PHOX2b Gen

H Prießmann1,
M Hammel2,
Rakhi Mittal3
et al.
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