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Smith–Lemli–Opitz syndrome with a classical phenotype, oesophageal achalasia and borderline plasma sterol concentrations

✍ Scribed by D. Haas; S. Armbrust; J.-P. Haas; J. Zschocke; K. Mühlmann; C. Fusch; L. M. Neumann


Book ID
106373895
Publisher
Springer
Year
2005
Tongue
English
Weight
188 KB
Volume
28
Category
Article
ISSN
0141-8955

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