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Assignment by Deletion Mapping of the Steroid Sulfatase X-linked Ichthyosis Locus to Xp223

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Journal Hum Genet
Specialty Genetics
Date 1980 Jan 1
PMID 6930361
Citations 69
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Abstract

A male child and his mother who are nullisomic and monosomic, respectively, for the distal portion of Xp because of an unbalanced X-Y translocation were tested for steroid sulfatase activity after clinical examination had yielded evidence for ichthyosis in the boy. Deficiency of steroid sulfatase was found in the male patient, while in his mother enzyme levels were in the heterozygous range. These results, based on cytogenetic evidence obtained with an elongation technique, indicate that the STS locus is at Xp 223.

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References
1.
Hameister H, Wolff G, Lauritzen C, Lehmann W, Hauser A, Ropers H . Clinical and biochemical investigations on patients with partial deficiency of placental steroid sulfatase. Hum Genet. 1979; 46(2):199-207. DOI: 10.1007/BF00291922. View

2.
Muller C, Migl B, Traupe H, Ropers H . X-linked steroid sulfatase: evidence for different gene-dosage in males and females. Hum Genet. 1980; 54(2):197-9. DOI: 10.1007/BF00278971. View

3.
Muller C, Westerveld A, Migl B, Franke W, Ropers H . Regional assignment of the gene locus for steroid sulfatase. Hum Genet. 1980; 54(2):201-4. DOI: 10.1007/BF00278972. View

4.
TIEPOLO L, Zuffardi O, Rodewald A . Nullisomy for the distal portion of Xp in a male child with a X/Y translocation. Hum Genet. 1977; 39(3):277-81. DOI: 10.1007/BF00295420. View

5.
Summitt R, Tipton R, Wilroy Jr R, Martens P, Phelan J . X-autosome translocations: a review. Birth Defects Orig Artic Ser. 1978; 14(6C):219-47. View