Acromicric Dysplasia Caused by a Novel Heterozygous Mutation of FBN1 and Effects of Growth Hormone Treatment
Annals of Laboratory Medicine
;
: 92-94, 2017.
Article
in English
| WPRIM
| ID: wpr-111447
ABSTRACT
No abstract available.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Pelvis
/
Bone Diseases, Developmental
/
Limb Deformities, Congenital
/
Human Growth Hormone
/
Fibrillin-1
/
Hand
/
Heterozygote
Limits:
Child
/
Humans
/
Male
Language:
English
Journal:
Annals of Laboratory Medicine
Year:
2017
Type:
Article
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