Segregation analysis in X-linked ichthyosis: paternal transmission of the affected X-chromosome
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2133.2007.08405.x/fullpdf
Reference13 articles.
1. Molecular heterogeneity of steroid sulfatase deficiency: A multicenter study on 57 unrelated patients, at DNA and protein levels
2. Molecular studies of deletions at the human steroid sulfatase locus.
3. Deletion pattern of the steroid sulphatase gene in Japanese patients with X-linked ichthyosis
4. Deletion patterns of the STS gene and flanking sequences in Israeli X-linked ichthyosis patients and carriers: analysis by polymerase chain reaction and fluorescence in situ hybridization techniques
5. Deletion Pattern of the STS Gene in X-linked Ichthyosis in a Mexican Population
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3. Genetic Study of X-Linked Recessive Ichthyosis in Eastern Ukraine;Cytology and Genetics;2021-01
4. A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients;BMC Medical Genetics;2020-01-31
5. X‐linked ichthyosis: Clinical and molecular findings in 35 Italian patients;Experimental Dermatology;2018-07-02
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