SRY mutation analysis by next generation (deep) sequencing in a cohort of chromosomal Disorders of Sex Development (DSD) patients with a mosaic karyotype
Remko Hersmus, Hans Stoop, Erin Turbitt, J Wolter Oosterhuis, Stenvert LS Drop, Andrew H Sinclair, Stefan J White, Leendert HJ Looijenga
BMC Medical Genetics | BIOMED CENTRAL LTD | Published : 2012
Awarded by Australian National Health and Medical Research Council Program Fellowship
This work was financially supported by Translational Research Grant Erasmus MC 2006 (RH), the Australian National Health and Medical Research Council Program Fellowship 491293 and Grant 546478 (SW) and supported by the Victorian Government's Operational Infrastructure Support Program (www.vic.gov.au) and the EuroDSD (www.eurodsd.eu).