反复纳差伴皮肤色素沉着2月余
Recurrent anorexia and pigmentation of skin for more than two months in an infant

DOI: 10.7499/j.issn.1008-8830.2017.08.015

Keywords: 复合型甘油激酶缺乏症,微阵列比较基因组杂交技术,Xp21邻近基因缺失综合征,婴儿,
Complex glycerol kinase deficiency,Array comparative genomic hybridization,Xp21 contiguous gene syndrome,Infant

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