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The gene for X-linked Kallmann syndrome: a human neuronal migration defect

✍ Scribed by Andrea Ballabio; Giovanna Camerino


Book ID
113404815
Publisher
Elsevier Science
Year
1992
Tongue
English
Weight
149 KB
Volume
2
Category
Article
ISSN
0960-9822

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Deletions of the steroid sulphatase gene
✍ A. Ballabio; G. Sebastio; R. Carrozzo; G. Parenti; A. Piccirillo; M. G. Persico; πŸ“‚ Article πŸ“… 1987 πŸ› Springer 🌐 English βš– 626 KB

We have studied 16 men, from 10 unrelated Italian families, affected by steroid suphatase (STS) deficiency, which is the basic defect of X-linked ichthyosis (XLI). The patients' clinical diagnoses were of either isolated ichthyosis or ichthyosis associated with Kallmann syndrome (KS) (hypogonadotrop