Banding Pattern on Polarized Hair Microscopic Examination and Unilateral Polymicrogyria in a Patient With Steroid Sulfatase Deficiency
Author:
Publisher
American Medical Association (AMA)
Subject
Dermatology,General Medicine
Cited by 12 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Inherited Disorders of Cornification;Rook's Textbook of Dermatology;2024-03-19
2. Maternal Xp22.31 copy-number variations detected in non-invasive prenatal screening effectively guide the prenatal diagnosis of X-linked ichthyosis;Frontiers in Genetics;2022-08-31
3. Hypertrophic pyloric stenosis masked by kidney failure in a male infant with a contiguous gene deletion syndrome at Xp22.31 involving the steroid sulfatase gene: case report;Italian Journal of Pediatrics;2022-02-03
4. X‐linked ichthyosis: Molecular findings in four pedigrees with inconspicuous clinical manifestations;Journal of Clinical Laboratory Analysis;2020-01-16
5. Mendelian Disorders of Cornification (MEDOC);Harper's Textbook of Pediatric Dermatology;2019-11-20
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