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Author/Creator Reho, Paolo

1. Clinical and Molecular Characteristics of SLC16A2 (MCT8) Mutations in Three Families with the Allan–Herndon–Dudley Syndrome. Issue 3 (5th January 2017)

Authors:
Novara, Francesca; Groeneweg, Stefan; Freri, Elena; Estienne, Margherita; Reho, Paolo; Matricardi, Sara; Castellotti, Barbara; Visser, W. Edward; Zuffardi, Orsetta; Visser, Theo J.
Journal:
Human mutation
Issue:
Volume 38:Issue 3(2017)
Page Start:
260
Record Type:
Journal Article
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6. Small supernumerary marker chromosomes: A legacy of trisomy rescue?. Issue 2 (22nd November 2018)

Authors:
Kurtas, Nehir Edibe; Xumerle, Luciano; Leonardelli, Lorena; Delledonne, Massimo; Brusco, Alfredo; Chrzanowska, Krystyna; Schinzel, Albert; Larizza, Daniela; Guerneri, Silvana; Natacci, Federica; Bonaglia, Maria Clara; Reho, Paolo; Manolakos, Emmanouil; Mattina, Teresa; Soli, Fiorenza; Provenzano,...
Journal:
Human mutation
Issue:
Volume 40:Issue 2(2019)
Page Start:
193
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗