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Acromicric Dysplasia Caused by a Novel Heterozygous Mutation of FBN1 and Effects of Growth Hormone Treatment
Hyung-Suk JIN; Ho-young SONG; Sung-Yoon CHO; Chang-Seok KI; Song-Hyun YANG; Ok-Hwa KIM; Su-Jin KIM.
Annals of Laboratory Medicine ; : 92-94, 2017.
Article in En | WPRIM | ID: wpr-111447
Responsible library: WPRO
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Full text: 1 Index: WPRIM Main subject: Pelvis / Bone Diseases, Developmental / Limb Deformities, Congenital / Human Growth Hormone / Fibrillin-1 / Hand / Heterozygote Limits: Child / Humans / Male Language: En Journal: Annals of Laboratory Medicine Year: 2017 Type: Article
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Full text: 1 Index: WPRIM Main subject: Pelvis / Bone Diseases, Developmental / Limb Deformities, Congenital / Human Growth Hormone / Fibrillin-1 / Hand / Heterozygote Limits: Child / Humans / Male Language: En Journal: Annals of Laboratory Medicine Year: 2017 Type: Article