Frequent deletions of the human X chromosome distal short arm result from recombination between low copy repetitive elements

Author:

Yen Pauline H.,Li Xiao-Miao,Tsai Siao-Ping,Johnson Carey,Mohandas T.,Shapiro Larry J.

Publisher

Elsevier BV

Subject

General Biochemistry, Genetics and Molecular Biology

Reference21 articles.

1. Molecular heterogeneity of steroid sulfatase deficiency: a multicenter study on 57 unrelated patients, at DNA and protein levels;Ballabio;Genomics,1989

2. Contiguous gene syndrome due to deletions in the distal short arm of the human X chromosome;Ballabio,1989

3. Cloning of a cDNA for steroid sulfatase: frequent occurrence of gene deletions in patients with recessive X chromosome-linked ichthyosis;Bonifas,1987

4. A rapid procedure for colony screening using nylon filters;Buluwela;Nucl. Acids Res.,1989

5. Genetic heterogeneity of steroid sulfatase deficiency revealed with cDNA for human steroid sulfatase;Conary;Biochem. Biophys. Res. Commun.,1987

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