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doi: 10.1007/bf02799196
pmid: 5726877
Two typical cases of anhidrotic ectodermal dysplasia occurring in heterosexual siblings of a family are reported. The role of consanguinity in the parents regarding the severity of the defect in these two siblings is stressed.
Male, Ectodermal Dysplasia, Child, Preschool, Humans, India, Infant, Female
Male, Ectodermal Dysplasia, Child, Preschool, Humans, India, Infant, Female
citations This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 17 | |
popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Average | |
influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 10% | |
impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Average |