Studying at the University of Verona

Here you can find information on the organisational aspects of the Programme, lecture timetables, learning activities and useful contact details for your time at the University, from enrolment to graduation.

The Study Plan includes all modules, teaching and learning activities that each student will need to undertake during their time at the University.
Please select your Study Plan based on your enrollment year.

2° Year  activated in the A.Y. 2020/2021

ModulesCreditsTAFSSD
7
B
INF/01 ,MED/40 ,MED/47
6
A/B/C
MED/20 ,MED/38 ,MED/47
5
B
BIO/14 ,MED/05 ,MED/09 ,MED/40 ,MED/49
8
A/B
MED/13 ,MED/17 ,MED/18 ,MED/24 ,MED/25 ,MED/47

3° Year  activated in the A.Y. 2021/2022

ModulesCreditsTAFSSD
4
B
MED/08 ,MED/15 ,MED/40 ,MED/47
6
A/B
MED/01 ,MED/40 ,MED/47
Final exam
7
E
-
activated in the A.Y. 2020/2021
ModulesCreditsTAFSSD
7
B
INF/01 ,MED/40 ,MED/47
6
A/B/C
MED/20 ,MED/38 ,MED/47
5
B
BIO/14 ,MED/05 ,MED/09 ,MED/40 ,MED/49
8
A/B
MED/13 ,MED/17 ,MED/18 ,MED/24 ,MED/25 ,MED/47

Legend | Type of training activity (TTA)

TAF (Type of Educational Activity) All courses and activities are classified into different types of educational activities, indicated by a letter.




S Placements in companies, public or private institutions and professional associations

Teaching code

4S000031

Credits

1

Language

Italian

Scientific Disciplinary Sector (SSD)

MED/03 - MEDICAL GENETICS

Period

1° ANNO 1° Semestre dal Oct 1, 2019 al Dec 8, 2019.

To show the organization of the course that includes this module, follow this link:  Course organization

Learning outcomes

Basic knowledge of human genetics. Understanding of the principles of hereditary transmission of normal and abnormal traits, as well as the origin of biological hereditary variation.

Program

Genomics, Genetics, Epigenetics
The human genome. Pedigrees. Mendelian inheritance. Non traditional inheritance.

Cytogenetics
Standard human karyotype. Anatomy of human chromosomes. Molecular cytogenetics (FISH, aCGH). Numerical and structural chromosome anomalies.

Clinical genetics and bioethics
Genetic counseling. Prenatal diagnosis. Preimplantation genetic diagnosis (PGD). Genetic testing. Stem cells and regenerative medicine. Bioethic and social issues.

Goals
Basic knowledge of human genetics. Understanding of the principles of hereditary transmission of normal and abnormal traits, as well as the origin of biological hereditary variation.

Reference texts
Author Title Publishing house Year ISBN Notes
Strachan T. and Read A. Human Molecular Genetics (Edizione 5) Garland Science (CRC press) 2018

Examination Methods

In order to pass the exam, students should demonstrate to have learned the necessary knowledges listed in the programme, to demonstrate skills in exposing their arguments in a critical and precise way, using an appropriate scientific language.
The Medical Genetics exam consists of a mutiple choice written test questions, open questions and exercises: 13 multiple choice questions, 5 answers (two points each), and two short open questions. The exam is passed if the score is equal to or greater than 18/30. The positive score is considered valid throughout the academic year. Six exams are planned yearly: two in Winter, 2 in Summer and 2 in Autumn.

Students with disabilities or specific learning disorders (SLD), who intend to request the adaptation of the exam, must follow the instructions given HERE