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Australian Paediatric Journal|October 1, 1988

Diagnosis of 21-hydroxylase deficiency in newborn infants by GC-MS of urinary steroidsA B Yong, J J Pitt, J Montalto, et al.

Clinical Endocrinology|January 1, 1990

Plasma C19 steroid sulphate levels and indices of androgen bioavailability in female pattern androgenic alopeciaJ Montalto, C B Whorwood, J W Funder, et al.

Proceedings of the National Academy of Sciences of the United States of America|November 11, 1999

Direct sequencing of bacterial and P1 artificial chromosome-nested deletions for identifying position-specific single-nucleotide polymorphismsP K Chatterjee, D P Yarnall, S A Haneline, et al.

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Search research articles

Showing results (11-20 of 13) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 13 results.

Australian Paediatric Journal|October 1, 1988

Diagnosis of 21-hydroxylase deficiency in newborn infants by GC-MS of urinary steroidsA B Yong, J J Pitt, J Montalto, et al.

Clinical Endocrinology|January 1, 1990

Plasma C19 steroid sulphate levels and indices of androgen bioavailability in female pattern androgenic alopeciaJ Montalto, C B Whorwood, J W Funder, et al.

Proceedings of the National Academy of Sciences of the United States of America|November 11, 1999

Direct sequencing of bacterial and P1 artificial chromosome-nested deletions for identifying position-specific single-nucleotide polymorphismsP K Chatterjee, D P Yarnall, S A Haneline, et al.

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