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Title: The turner phenotype and the different types of human X isochromosome
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Human Genetics [0340-6717] Larizza, Daniela yr:1982


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1. Larizza, D. "Adrenocorticotrophin stimulation and HLA polymorphisms suggest a high frequency of heterozygosity for steroid 21-hydroxylase deficiency in patients with Turner's syndrome and their families." Clinical endocrinology 40.1 (1994): 39-45. Link to SFX for this item
2. Maciel Guerra, A P T. "Female pseudohermaphroditism due to classical 21-hydroxylase deficiency in a girl with Turner syndrome." Clinical genetics 51.5 (1997): 351-353. Link to Full Text for this item Link to SFX for this item
3. Keskin, M. "Female pseudohermaphroditism due to classical 21-hydroxylase deficiency and insulin resistance in a girl with Turner syndrome." The Turkish journal of pediatrics 47.2 (2005): 176-9. Link to SFX for this item
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