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Ulivi, Sheila
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Preferred name
Ulivi, Sheila
Main Affiliation
Email
sheila.ulivi@burlo.trieste.it
ORCID
Scopus Author ID
24598313400
Researcher ID
H-3700-2013
Research Output
Now showing 1 - 4 of 4
- PublicationIdentification of a new mutation in RSK2, the gene for coffin¿lowry syndrome (CLS), in two related patients with mild and atypical phenotypes
; ; ; - PublicationGenetic insights into biological mechanisms governing human ovarian ageing
; ; ; ; - PublicationCase Report: Two cases of apparent discordance between non-invasive prenatal testing (NIPT) and amniocentesis resulting in feto-placental mosaicism of trisomy 21. Issues in diagnosis, investigation and counselling
; ; ; ; - PublicationGenome-wide association studies on Northern Italy isolated populations provide further support concerning genetic susceptibility for major depressive disorder
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