Author:
Ballabio A.,Sebastio G.,Carrozzo R.,Parenti G.,Piccirillo A.,Persico M. G.,Andria G.
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference35 articles.
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2. Andria G, Ballabio A, Parenti G, Di Maio S, Piccirillo A (1984b) Steroid sulphatase deficiency is present in patients with X-linked ?ichthyosis and male hypogonadism? and with ?Rud syndrome?. J Inherited Metab Dis [Suppl 2] 7:158?160
3. Ballabio A, Parenti G, Napolitano E, Di Natale P, Andria G (1985) Genetic complementation of steroid sulphatase after somatic cell hybridization of X-linked ichthyosis and multiple sulphatase deficiency. Hum Genet 70:315?317
4. Ballabio A, Parenti G, Tippett P, Mondello C, Di Maio S, Tenore A, Andria G (1986) X-linked ichthyosis, due to steroid sulphatase deficiency, associated with Kallmann syndrome (hypogonadotropic hypogonadism and anosmia): linkage relationships with Xg and cloned DNA sequences from the distal short arm of the X chromosome. Hum Genet 72:237?240
5. Ballabio A, Parenti G, Carrozzo R, Sebastio G, Andria G, Buckle V, Fraser N, Boyd Y, Craig I, Rocchi M, Romeo G, Jobsis AC, Persico MG (1987) Isolation and characterisation of a steroid sulphatase cDNA clone; genomic deletions in patients with X-linked ichthyosis. Proc Natl Acad Sci USA 84:4519?4523
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