Benign anomaly to malign dysplasia: variable expression of lamin B receptor mutations in humans.
J Biosci
;
2004 Dec; 29(4): 367-8
Article
in English
| IMSEAR
| ID: sea-111062
Subject(s)
Full text:
Available
Index:
IMSEAR (South-East Asia)
Main subject:
Pelger-Huet Anomaly
/
Phenotype
/
Bone Diseases, Developmental
/
Humans
/
Receptors, Cytoplasmic and Nuclear
/
Animals
/
Mice
Language:
English
Journal:
J Biosci
Year:
2004
Type:
Article
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