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Hypochondroplasia due to FGFR3 gene mutation (N540K) and mosaic form of Down syndrome in the same patient

✍ Scribed by Katja Dumic; Ingeborg Barisic; Kristina Potocki; Ivona Sansovic


Book ID
107700445
Publisher
Springer-Verlag
Year
2011
Tongue
English
Weight
146 KB
Volume
52
Category
Article
ISSN
1234-1983

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