Related content

A 46,XX Ovotesticular Disorder of Sex Development Likely Caused by a Steroidogenic Factor-1 (NR5A1) Variant

By  

Hormone Research in Paediatrics, Vol. 87, Iss. 3, 2016-11 ,pp. : 191-195

Karger

Access to resources Recommend Favorite

Preserved Fertility in a Patient with a 46,XY Disorder of Sex Development due to a New Heterozygous Mutation in the NR5A1/SF-1 Gene: Evidence of 46,XY and 46,XX Gonadal Dysgenesis Phenotype Variability in Multiple Members of an Affected Kindred

By  

Hormone Research in Paediatrics, Vol. 78, Iss. 2, 2012-08 ,pp. : 119-126

Karger

Access to resources Recommend Favorite

Novel Heterozygous Mutations of NR5A1 and Their Functional Characteristics in Patients with 46,XY Disorders of Sex Development without Adrenal Insufficiency

By  

Hormone Research in Paediatrics, Vol. 84, Iss. 2, 2015-06 ,pp. : 116-123

Karger

Access to resources Recommend Favorite

Three New SF-1 (NR5A1) Gene Mutations in Two Unrelated Families with Multiple Affected Members: Within-Family Variability in 46,XY Subjects and Low Ovarian Reserve in Fertile 46,XX Subjects

By  

Hormone Research in Paediatrics, Vol. 75, Iss. 1, 2010-09 ,pp. : 70-77

Karger

Access to resources Recommend Favorite

NR5A1 Gene Mutations: Clinical, Endocrine and Genetic Features in Two Girls with 46,XY Disorder of Sex Development

By  

Hormone Research in Paediatrics, Vol. 81, Iss. 2, 2014-01 ,pp. : 104-108

Karger

Access to resources Recommend Favorite