Prevalence of endocrine and genetic abnormalities in boys evaluated systematically for a disorder of sex development

Author:

Nixon R.1,Cerqueira V.2,Kyriakou A.1,Lucas-Herald A.1,McNeilly J.3,McMillan M.1,Purvis A.I.2,Tobias E.S.24,McGowan R.12,Ahmed S.F.1ORCID

Affiliation:

1. Developmental Endocrinology Research Group, University of Glasgow, Royal Hospital for Children, Office Block, 1345 Govan Road, Glasgow G51 4TF, UK

2. West of Scotland Clinical Genetics Service, Queen Elizabeth University Hospital, Glasgow G51 4TF, UK

3. Biochemistry Department, Queen Elizabeth University Hospital, Glasgow G51 4TF, UK

4. Academic Medical Genetics and Pathology, University of Glasgow, Queen Elizabeth University Hospital, Glasgow G51 4TF, UK

Funder

James Paterson Bursary

Glasgow Children's Hospital Charity Summer Scholarship

Scottish Executive Health Department

MRC/EPSRC Molecular Pathology Node

Wellcome Trust ISSF funding

Publisher

Oxford University Press (OUP)

Subject

Obstetrics and Gynecology,Rehabilitation,Reproductive Medicine

Reference29 articles.

1. Assessment of the gonadotrophin-gonadal axis in androgen insensitivity syndrome;Ahmed;Arch Dis Child,1999

2. Phenotypic features, androgen receptor binding, and mutational analysis in 278 clinical cases reported as androgen insensitivity syndrome;Ahmed;J Clin Endocrinol Metab,2000

3. The role of a clinical score in the assessment of ambiguous genitalia;Ahmed;BJU Int,2000

4. The testosterone:androstendione ratio in male undermasculinization;Ahmed;Clin Endocrinol,2000

5. Investigation and initial management of ambiguous genitalia;Ahmed;Best Pract Res Clin Endocrinol Metab,2010

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