The molecular genetics of androgen insensitivity syndrome
The aim of this project was to identify and characterise the AR gene defect responsible for AIS in a cohort of fourteen patients with the complete form of the syndrome. The chosen method for mutation detection was fluorescent semi-automated sequence analysis of the entire coding region of the gene....
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University of Cambridge
1997
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| Online Access: | http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.598354 |