Breast Carcinoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
Cloning and mutation analysis of ZFP276 as a candidate tumor suppressor in breast cancer.
|
14605947 |
2003 |
Fanconi Anemia
|
0.110 |
GeneticVariation
|
disease |
CLINVAR |
Validation of Fanconi anemia complementation Group A assignment using molecular analysis.
|
19367192 |
2009 |
Fanconi Anemia
|
0.110 |
CausalMutation
|
disease |
CLINVAR |
Sequence variation in the Fanconi anemia gene FAA.
|
9371798 |
1997 |
Fanconi Anemia
|
0.110 |
GeneticVariation
|
disease |
CLINVAR |
Clinical utility of next-generation sequencing for inherited bone marrow failure syndromes.
|
28102861 |
2017 |
Fanconi Anemia
|
0.110 |
GeneticVariation
|
disease |
CLINVAR |
Genetic subtyping of Fanconi anemia by comprehensive mutation screening.
|
17924555 |
2008 |
Fanconi Anemia
|
0.110 |
CausalMutation
|
disease |
CLINVAR |
Spectrum of sequence variations in the FANCA gene: an International Fanconi Anemia Registry (IFAR) study.
|
15643609 |
2005 |
Fanconi Anemia
|
0.110 |
GeneticVariation
|
disease |
CLINVAR |
A comprehensive approach to identification of pathogenic FANCA variants in Fanconi anemia patients and their families.
|
29098742 |
2018 |
Fanconi Anemia
|
0.110 |
GeneticVariation
|
disease |
CLINVAR |
Molecular analysis of Fanconi anemia: the experience of the Bone Marrow Failure Study Group of the Italian Association of Pediatric Onco-Hematology.
|
24584348 |
2014 |
Fanconi Anemia
|
0.110 |
GeneticVariation
|
disease |
CLINVAR |
A strategy for molecular diagnostics of Fanconi anemia in Brazilian patients.
|
28717661 |
2017 |
Fanconi Anemia
|
0.110 |
GeneticVariation
|
disease |
CLINVAR |
Origin, functional role, and clinical impact of Fanconi anemia FANCA mutations.
|
21273304 |
2011 |
Fanconi Anemia
|
0.110 |
Biomarker
|
disease |
BEFREE |
The overlapping genomic organization between Zfp276 and Fanca may have relevance to the disease phenotype of FA.
|
10936049 |
2000 |
Fanconi Anemia
|
0.110 |
GeneticVariation
|
disease |
CLINVAR |
Heterogeneous spectrum of mutations in the Fanconi anaemia group A gene.
|
10094191 |
1999 |
Fanconi Anemia
|
0.110 |
GeneticVariation
|
disease |
CLINVAR |
Spectrum of sequence variations in the FANCA gene: an International Fanconi Anemia Registry (IFAR) study.
|
15643609 |
2005 |
Fanconi Anemia
|
0.110 |
CausalMutation
|
disease |
CLINVAR |
Origin, functional role, and clinical impact of Fanconi anemia FANCA mutations.
|
21273304 |
2011 |
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
0.110 |
GeneticVariation
|
disease |
CLINVAR |
A strategy for molecular diagnostics of Fanconi anemia in Brazilian patients.
|
28717661 |
2017 |
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
0.110 |
GeneticVariation
|
disease |
CLINVAR |
Spectrum of sequence variations in the FANCA gene: an International Fanconi Anemia Registry (IFAR) study.
|
15643609 |
2005 |
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
0.110 |
GeneticVariation
|
disease |
CLINVAR |
Variant ALDH2 is associated with accelerated progression of bone marrow failure in Japanese Fanconi anemia patients.
|
24037726 |
2013 |
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
0.110 |
CausalMutation
|
disease |
CLINVAR |
A comprehensive approach to identification of pathogenic FANCA variants in Fanconi anemia patients and their families.
|
29098742 |
2018 |
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
0.110 |
CausalMutation
|
disease |
CLINVAR |
Molecular characterization of three novel Fanconi anemia mutations in Israeli Arabs.
|
15059067 |
2004 |
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
0.110 |
GeneticVariation
|
disease |
CLINVAR |
Sequence variation in the Fanconi anemia gene FAA.
|
9371798 |
1997 |
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
0.110 |
GeneticVariation
|
disease |
CLINVAR |
Origin, functional role, and clinical impact of Fanconi anemia FANCA mutations.
|
21273304 |
2011 |
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
0.110 |
CausalMutation
|
disease |
CLINVAR |
Fanconi anemia signaling network regulates the spindle assembly checkpoint.
|
23934222 |
2013 |
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
0.110 |
CausalMutation
|
disease |
CLINVAR |
Origin, functional role, and clinical impact of Fanconi anemia FANCA mutations.
|
21273304 |
2011 |
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
0.110 |
CausalMutation
|
disease |
CLINVAR |
Profiling Fanconi Anemia Gene Mutations among Iranian Patients.
|
27041517 |
2016 |
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
0.110 |
GeneticVariation
|
disease |
CLINVAR |
Heterogeneous activation of the Fanconi anemia pathway by patient-derived FANCA mutants.
|
12444097 |
2002 |