A Molecular, Genetic, and Diagnostic Spotlight on Fanconi Anemia
Saved in:
Main Authors: | Laura E. Hays, Stefan Meyer, Henri J. van de Vrugt |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2012-01-01
|
Series: | Anemia |
Online Access: | http://dx.doi.org/10.1155/2012/650730 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Towards a Molecular Understanding of the Fanconi Anemia Core Complex
by: Charlotte Hodson, 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: Chromosomal Breakage Analysis
by: Anneke B. Oostra, et al.
Published: (2012-01-01) -
Targeting the Fanconi Anemia Pathway to Identify Tailored Anticancer Therapeutics
by: Chelsea Jenkins, et al.
Published: (2012-01-01) -
Oral Squamous Cell Carcinoma in a Patient with Fanconi Anemia
by: Milla Huuhka, et al.
Published: (2021-01-01)