1. Complete gonadal dysgenesis in clinical practice: the 46,XY karyotype accounts for more than one third of cases 
Vanessa Brito Campoy Rocha, Gil Guerra-Júnior, M.D., Ph.D., Antonia Paula Marques-de-Faria, M.D., Ph.D., Maricilda Palandi de Mello, Ph.D., Andréa Trevas Maciel-Guerra, M.D., Ph.D. 
Fertility and Sterility 
Volume 96, Issue 6, Pages (December 2011)
DOI: /j.fertnstert
Copyright © 2011 American Society for Reproductive Medicine Terms and Conditions

2. Figure 1
Pedigrees of nine families with complete gonadal dysgenesis (CGD) and parental consanguinity. (A–G) 46,XX CGD; (H and I) 46,XY CGD (cases 7 and 8, respectively—see Table 1). Solid circles represent individuals with complete gonadal dysgenesis and female phenotype, and the square containing a solid circle represents an individual with sex ambiguity who was raised as a girl.
Fertility and Sterility  , DOI: ( /j.fertnstert )
Copyright © 2011 American Society for Reproductive Medicine Terms and Conditions