Results 131 to 140 of about 1,183,898 (170)

A Clinical Genetics-Driven Dual Diagnosis of Prader-Willi Syndrome Due to Mosaic Maternal UPD(15) and <i>NOTCH3</i>-Related CADASIL. [PDF]

open access: yesGenes (Basel)
Bogliardi FM   +10 more
europepmc   +1 more source

Early neurodevelopmental brain perfusion abnormalities and functional connectivity findings in infants with Prader-Willi syndrome. [PDF]

open access: yesJ Neurodev Disord
Boisgontier J   +14 more
europepmc   +1 more source

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