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Paper Details

Split hand/foot malformation associated with 20p12.1 deletion: A case report.
Eur J Med Genet
1
2020
Author NameAffiliation
Malte SpielmannCharite - Universitatsmedizin Berlin, Institut fur Medizinische Genetik
Stefan MundlosCharite - Universitatsmedizin Berlin, Institut fur Medizinische Genetik
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Datasets

Release 1.2