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检索条件"主题词=familial hypotrichosis"
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Autozygosity Mapping by Genome-wide Single Nucleotide Polymorphism Array Identifies a Novel Homozygous HR Mutation in a Consanguineous Family with Universal Hereditary Hair Loss
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International Journal of Dermatology and Venereology 2021年 第2期4卷 82-85页
作者: Sirous Zeinali Leila Youssefian Hassan Vahidnezhad Amir Hossein Saeidian Soheila Sotoudeh Hamideh Bagherian Jouni Uitto Department of Molecular Medicine Biotechnology Research CenterPasteur Institute of IranTehranIran Kawsar Human Genetics Research Center TehranIran Department of Dermatology and Cutaneous Biology Sidney Kimmel Medical Collegeand Jefferson Institute of Molecular MedicineThomas Jefferson UniversityPhiladelphiaPA 19107USA Department of Medical Genetics School of MedicineTehran University of Medical SciencesTehranIran Department of Dermatology Children’s Medical CenterCenter of ExcellenceTehran University of Medical SciencesTehranIran
Objective:Isolated hereditary hypotrichosis is caused by mutations in as many as 11 different *** conventional mutation detection strategy consists of sequencing of individual candidate genes separately,a time consumi... 详细信息
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