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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
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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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