A Dutch Fanconi Anemia FANCC Founder Mutation in Canadian Manitoba Mennonites
Fanconi anemia (FA) is a recessive DNA instability disorder associated with developmental abnormalities, bone marrow failure, and a predisposition to cancer. Based on their sensitivity to DNA cross-linking agents, FA cells have been assigned to 15 complementation groups, and the associated genes hav...
Saved in:
Main Authors: | Yne de Vries, Nikki Lwiwski, Marieke Levitus, Bertus Kuyt, Sara J. Israels, Fré Arwert, Michel Zwaan, Cheryl R. Greenberg, Blanche P. Alter, Hans Joenje, Hanne Meijers-Heijboer |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2012-01-01
|
Series: | Anemia |
Online Access: | http://dx.doi.org/10.1155/2012/865170 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Diagnosis of Fanconi Anemia: Chromosomal Breakage Analysis
by: Anneke B. Oostra, et al.
Published: (2012-01-01) -
Diagnostic Overlap between Fanconi Anemia and the Cohesinopathies: Roberts Syndrome and Warsaw Breakage Syndrome
by: Petra van der Lelij, et al.
Published: (2010-01-01) -
Diagnosis of Fanconi Anemia: Mutation Analysis by Multiplex Ligation-Dependent Probe Amplification and PCR-Based Sanger Sequencing
by: Johan J. P. Gille, et al.
Published: (2012-01-01) -
Old Colony Mennonites in Argentina and Bolivia. Nation Making, Religious Conflict and Imagination of the Future
by: Aimar Ventsel
Published: (2011-03-01) -
A Molecular, Genetic, and Diagnostic Spotlight on Fanconi Anemia
by: Laura E. Hays, et al.
Published: (2012-01-01)