Albinism: modern molecular diagnosis.
作者信息
Carden S M, Boissy R E, Schoettker P J, Good W V
机构信息
Royal Children's Hospital, Melbourne, Australia.
出版信息
Br J Ophthalmol. 1998 Feb;82(2):189-95. doi: 10.1136/bjo.82.2.189.
Abstract
摘要
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本文引用的文献
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Tyrosinase activity in melanocytes of human albinos.人类白化病患者黑素细胞中的酪氨酸酶活性。
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Molecular basis of congenital hypopigmentary disorders in humans: a review.人类先天性色素减退症的分子基础：综述
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Positional cloning of a gene for Hermansky-Pudlak syndrome, a disorder of cytoplasmic organelles.一种细胞质细胞器疾病——赫尔曼斯基-普德拉克综合征相关基因的定位克隆
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Genetic and physical mapping of the Chediak-Higashi syndrome on chromosome 1q42-43.切-东综合征在1号染色体1q42-43区域的遗传与物理图谱分析
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Ocular findings in the Hermansky-Pudlak syndrome.Hermansky-Pudlak综合征的眼部表现
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Identification of the homologous beige and Chediak-Higashi syndrome genes.同源米色基因和切迪阿克-东综合征基因的鉴定。
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