熊慧

工作机构：厦门基源医学检验实验室

专业：基础医学

ATP7A-Related Copper Transport Disorders	ATP7A-Related Copper Transport Disorders	NBKID:
Atelosteogenesis Type 2	Atelosteogenesis Type 2	NBKID:
Autosomal Recessive Congenital Ichthyosis	Autosomal Recessive Congenital Ichthyosis	NBKID:
Citrin Deficiency	Citrin Deficiency	NBKID:
Congenital Stromal Corneal Dystrophy	Congenital Stromal Corneal Dystrophy	NBKID:
DEPDC5-Related Epilepsy	DEPDC5 相关癫痫	NBKID:
FRMD7-Related Infantile Nystagmus	FRMD7-Related Infantile Nystagmus	NBKID:
Familial Exudative Vitreoretinopathy, Autosomal Dominant	Familial Exudative Vitreoretinopathy, Autosomal Dominant	NBKID:
Floating-Harbor Syndrome	Floating-Harbor综合征	NBKID:
Krabbe Disease	Krabbe Disease	NBKID:
Leber Hereditary Optic Neuropathy	Leber Hereditary Optic Neuropathy	NBKID:
MECP2-Related Disorders	MECP2 -相关疾病	NBKID:
Myotonic Dystrophy Type 1	Myotonic Dystrophy Type 1	NBKID:
Myotonic Dystrophy Type 2	Myotonic Dystrophy Type 2	NBKID:
Retinoblastoma	Retinoblastoma	NBKID:
VCAN-Related Vitreoretinopathy	VCAN-Related Vitreoretinopathy	NBKID:
Wilson Disease	Wilson Disease	NBKID:
X-Linked Congenital Stationary Night Blindness	X-Linked Congenital Stationary Night BlindnessX连锁先天性静止性夜盲	NBKID:

中文版GeneReviews