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Genetic diagnosis of 21-hydroxylase deficiency: DGGE-based mutation scanning of CYP21.
Ohlsson, G; Müller, J; Schwartz, M.
Affiliation
  • Ohlsson G; Department of Clinical Genetics, Juliane Marie Center, University Hospital, Rigshospitalet, Copenhagen, Denmark. olsson@biobase.dk
Hum Mutat ; 13(5): 385-9, 1999.
Article in En | MEDLINE | ID: mdl-10338093
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Collection: 01-internacional Database: MEDLINE Main subject: DNA Mutational Analysis / Adrenal Hyperplasia, Congenital / Cytochrome P-450 CYP2B1 / Electrophoresis, Polyacrylamide Gel Type of study: Diagnostic_studies Limits: Humans Language: En Journal: Hum Mutat Journal subject: GENETICA MEDICA Year: 1999 Document type: Article Affiliation country: Denmark Country of publication: United States
Search on Google
Add to My VHL
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XML
PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: DNA Mutational Analysis / Adrenal Hyperplasia, Congenital / Cytochrome P-450 CYP2B1 / Electrophoresis, Polyacrylamide Gel Type of study: Diagnostic_studies Limits: Humans Language: En Journal: Hum Mutat Journal subject: GENETICA MEDICA Year: 1999 Document type: Article Affiliation country: Denmark Country of publication: United States