Λίστα αντικειμένων
Germ-line missense mutations in PTPN11, the gene coding SHP-2, have been discovered as a major molecular event underlying Noonan syndrome, an autosomal dominant trait characterized by short stature, dysmorphic facies, and congenital heart defects, as well as in other closely related
developmental disorders. More recently, a distinct class of missense mutations in the same gene has been identified to occur as a somatic event contributing to myeloid and lymphoid malignancies.
The review was presented and discusssed.
Presenter: Prof Spyridonidis
Participants: Dr Liga, Dr Tsokanas, Dr Valera
Duration: 40 mins
developmental disorders. More recently, a distinct class of missense mutations in the same gene has been identified to occur as a somatic event contributing to myeloid and lymphoid malignancies.
The review was presented and discusssed.
Presenter: Prof Spyridonidis
Participants: Dr Liga, Dr Tsokanas, Dr Valera
Duration: 40 mins
Σχετικά Αρχεία
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Γραμματεία MMMO: 2613 603506 (ασθενείς), 2613 604062 (Γραμματεία Διευθυντή) Fax : 2613 604066,email (για ιατρούς): transplant@upatras.gr,
email (για ασθενείς): mmak@upatras.gremail (για θέματα κλινικών μελετών) : gcppatras@gmail.comΜονάδα Μεταμόσχευσης (Νοσηλεία): 2613 603 261Γραφείο Ιατρών: 2613 604064, 2613 604065, Εφημερεύων Ιατρός: 2610 999111 (τηλ. κέντρο ΠΓΝΠ)
