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EUROPEAN JOURNAL OF MEDICAL GENETICS
Rivista
Codice:
E188690
ISSN:
1769-7212
Dati Generali
Dati Generali
Pubblicazioni (6)
ADDing a piece to the puzzle of cognition in schizophrenia
Articolo
Chiari I malformation in a child with PTEN hamartoma tumor syndrome: Association or coincidence?
Articolo
Clinical and molecular characterization of a novel INS mutation identified in patients with MODY phenotype
Articolo
Metatropic dysplasia in third trimester of pregnancy and a novel causative variant in the TRPV4 gene
Articolo
Novel TBX3 mutation data in families with Ulnar-Mammary syndrome indicate a genotype-phenotype relationship: mutations that do not disrupt the T-domain are associated with less severe limb defects
Articolo
SMARCE1-related meningiomas: A clear example of cancer predisposing syndrome
Articolo
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