Loading...

Diagnosis of Fanconi Anemia: Chromosomal Breakage Analysis

Fanconi anemia (FA) is a rare inherited syndrome with diverse clinical symptoms including developmental defects, short stature, bone marrow failure, and a high risk of malignancies. Fifteen genetic subtypes have been distinguished so far. The mode of inheritance for all subtypes is autosomal recessi...

Fuld beskrivelse

Na minha lista:
Bibliografiske detaljer
Main Authors: Oostra, Anneke B., Nieuwint, Aggie W. M., Joenje, Hans, de Winter, Johan P.
Format: Artigo
Sprog:Inglês
Udgivet: Hindawi Publishing Corporation 2012
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3368163/
https://ncbi.nlm.nih.gov/pubmed/22693659
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2012/238731
Tags: Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!