X-Linked Ichthyosis

Author:

Chen Harold

Publisher

Springer New York

Reference30 articles.

1. Ahmed, M. N., Killam, A., Thompson, K. H., et al. (1998). Unconjugated estriol as an indication for prenatal diagnosis of steroid sulfatase deficiency by in situ hybridization. Obstetrics and Gynecology, 92, 687–689.

2. Aviram-Goldring, A., Goldman, B., Netanelov-Shapira, I., et al. (2000). 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. International Journal of Dermatology, 39, 182–187.

3. Basler, E., Grompe, M., Parenti, G., et al. (1992). Identification of point mutations in the steroid sulfatase gene of three patients with X-linked ichthyosis. American Journal of Human Genetics, 50, 483–491.

4. Bonifas, J. M., & Epstein, E. H., Jr. (1990). Detection of carriers for X-linked ichthyosis by Southern blot analysis and identification of one family with a de novo mutation. The Journal of Investigative Dermatology, 95, 16–19.

5. Bradshaw, K. D., & Carr, B. R. (1986). Placental sulfatase deficiency: Maternal and fetal expression of steroid sulfatase deficiency and X-linked ichthyosis. Obstetrical and Gynecological Survey, 41, 401–413.

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