SINDROMUL LEOPARD. CAZURI FAMILIALE

SINDROMUL LEOPARD. CAZURI FAMILIALE

Sindromul LEOPARD este o afecţiune ce include multiple anomalii dismorfogenetice. Sindromul LEOPARD, ca şi sindromul Noonan, este determinat de mutaţii ale genei PTPN11. Autorii menţionează particularităţile diagnostice la 2 cazuri înrudite cu dismorfi sm facial. Cazul index este reprezentat...

Full description

Saved in:
Bibliographic Details
Main Authors: Sorin Ioan Iurian (Author), Han Brunner (Author), Helger Yntema (Author), Bogdan Mehedinţu (Author)
Format: Book
Published: Amaltea Medical Publishing House, 2014-03-01T00:00:00Z.
Subjects:
article
Online Access:Connect to this object online.
Tags: Add Tag
No Tags, Be the first to tag this record!

Internet

Connect to this object online.

3rd Floor Main Library

Holdings details from 3rd Floor Main Library
Call Number: A1234.567
Copy 1 Available

Similar Items