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MO059COLEC10 AND 3MC SYNDROME: EXPANDING THE GENOTYPIC AND PHENOTYPIC SPECTRUM OF A VERY RARE DISEASE
MO059COLEC10 AND 3MC SYNDROME: EXPANDING THE GENOTYPIC AND PHENOTYPIC SPECTRUM OF A VERY RARE DISEASE
2021
Martina Migliorero
Silvia Kalantari
Valeria Bracciamà
Monica Sorbini
Francesca Arruga
Licia Peruzzi
Elisa Biamino
Antonio Amoroso
Tiziana Vaisitti
Silvia Deaglio
Keywords:
Rare disease
3MC syndrome
Medicine
Genotype
Genetics
umbilicus
Phenotype
Correction
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