Search

Author/Creator Leto, F.

2. Coheredity of a new silent mutation: c.‐29G>T, with a severe β‐thal mutation in a patient with β‐thalassemia intermediate. (5th February 2018)

Authors:
Vinciguerra, M.; Passarello, C.; Cassarà, F.; Leto, F.; Cannata, M.; Calvaruso, G.; Renda, D.; Maggio, A.; Giambona, A.
Journal:
International journal of laboratory hematology
Issue:
Volume 40:Number 2(2018:Apr.)
Page Start:
e17
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. Co‐heredity of silent CAP + 1570 T>C (HBB:c*96T>C) defect and severe β‐thal mutation: a cause of mild β‐thalassemia intermedia. (29th September 2015)

Authors:
Vinciguerra, M.; Passarello, C.; Cassarà, F.; Leto, F.; Cannata, M.; Calvaruso, G.; Di Maggio, R.; Renda, D.; Maggio, A.; Giambona, A.
Journal:
International journal of laboratory hematology
Issue:
Volume 38:Number 1(2016:Feb.)
Page Start:
17
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

4. Incidence of haemoglobinopathies in Sicily: the impact of screening and prenatal diagnosis. Issue 10 (27th February 2015)

Authors:
Giambona, A.; Damiani, G.; Vinciguerra, M.; Jakil, C.; Cannata, M.; Cassarà, F.; Picciotto, F.; Schillaci, G.; Cigna, V.; Renda, D.; Leto, F.; Passarello, C.; Maggio, A.
Journal:
International journal of clinical practice
Issue:
Volume 69:Issue 10(2015)
Page Start:
1129
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗