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August 2022 in “Dermatologic Therapy”
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4 citations
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March 2007 in “Hair transplant forum international” The document's conclusion cannot be provided as the content is not available.
July 2024 in “Reactions Weekly”
January 2025 in “Dermatology Reports” Early and accurate diagnosis is crucial for managing rare genetic disorders like this localized variant of junctional epidermolysis bullosa.
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December 2006 in “Mammalian Genome” October 2025 in “Skin Research and Technology”
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August 2025 in “BMC Pregnancy and Childbirth” A new EDA gene variant causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family.
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December 2017 in “The Journal of Dermatology” A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.
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