Fini, Sergio
91  Ergebnisse:
Personensuche X
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1

Koolen‐de Vries syndrome in a 63‐year‐old woman: Report of ..:

Farnè, Marianna ; Bernardini, Laura ; Capalbo, Anna...
American Journal of Medical Genetics Part A.  188 (2021)  2 - p. 692-707 , 2021
 
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3

New patients with Temple syndrome caused by 14q32 deletion:..:

Severi, Giulia ; Bernardini, Laura ; Briuglia, Silvana...
American Journal of Medical Genetics Part A.  170 (2015)  1 - p. 162-169 , 2015
 
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5

A three-generation family with terminal microdeletion invol..:

Elmakky, Amira ; Carli, Diana ; Lugli, Licia...
European Journal of Medical Genetics.  57 (2014)  4 - p. 145-150 , 2014
 
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6

Downregulation of A1 and A2B adenosine receptors in human t..:

Gessi, Stefania ; Merighi, Stefania ; Stefanelli, Angela...
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease.  1822 (2012)  11 - p. 1660-1670 , 2012
 
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12

A novel custom high density-comparative genomic hybridizati..:

BOVOLENTA, Matteo ; NERI, Marcella ; FINI, Sergio...
info:eu-repo/semantics/altIdentifier/wos/WOS:000262194800003.  , 2008
 
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