Lv41
540 积分 2025-03-04 加入
Congenital monilethrix and hereditary unilateral external auditory canal atresia are co‐inherited in a Chinese pedigree with recurrent KRT86 mutation
1小时前
已完结
Mutation E402K of the hHb6 in a Chinese Han family with monilethrix
1小时前
已完结
Masquerading of trichotillomania in a family with monilethrix
1小时前
已完结
Identification of a novel missense KRT86 mutation in a Chinese family with monilethrix
1小时前
已完结
Monilethrix in monozygotic twins with very rare mutation in KRT 86 gene
2小时前
求助中
Monilethrix: A case report imaged by trichoscopy, reflectance confocal microscopy and histopathology
2小时前
求助中
Monilethrix
2小时前
已完结
Image Gallery: Unusual images of monilethrix: the eyebrows and the biopsy
2小时前
求助中
Recessive progressive symmetric erythrokeratoderma results from a homozygous loss-of-function mutation of KRT83 and is allelic with dominant monilethrix
2小时前
求助中
Novel D323G mutation of DSG4 gene in a girl with localized autosomal recessive hypotrichosis clinically overlapped with monilethrix
2小时前
已完结
Innovative resource management for strategic entrepreneurship and competitive advantage
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