Humpath.com - Human pathology

A. Molecular pathology
B. Cellular pathology
C. Tissular pathology
D. General pathology
E. Pathology by systems
F. Pathology by regions
G. Tumoral pathology
H. Case records
K. Info - Admin
Resources in pathology
Technical section

Home > A. Molecular pathology > HOXA11

HOXA11

MIM.142958 7p15-p14.2

Friday 30 November 2007

Pathology

germline mutations in autosomal dominant radioulnar synostosis with amegakaryocytic thrombocytopenia (MIM.605432)

A. Molecular pathology

CDs
Exosome
Fusion genes
IHC markers
Metabolome
miRNAs
ncRNAs
Signaling pathways
Systems medicine
Targeted therapy
tRNAs
Variants-Mutants

Search:

Also in this section

energy
Precambrian
organic chemistry
organic transformation
chemical reaction
catalysis
PI3K
BCL10
cathepsin-K
MUC5B

Keywords

Mutated in human diseases
Protein

1996 - 2022 Humpath.com - Human pathology
Site Map | Log in | Contact | RSS 2.0