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Molecular Syndromology
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Latest
Most Read
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Erratum - Investigation of Genetic Changes in Three Families with Bipolar Disease
Kabuki Syndrome and Charcot-Marie-Tooth Disease Co-Occurrence: Unique Case with Novel Variant
A Novel Loss-of-Function Variant in COL4A3 in a Consanguineous Moroccan Family Displaying the Alport Syndrome with Variable Clinical Expression
Homozygous Intragenic Deletion in
WDR62
in Siblings with Primary Microcephaly
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