This site will help parents and patients understand intersexuality and the challenges that accompany syndromes of "abnormal" sex differentiation. From the Johns Hopkins C...
http://www.hopkinsmedicine.org/pediatricendocrinology/
Klinfelter's support site. Designed to provide support and education for families and professionals dealing with these genetic conditions, including sex chromosome variations 47XXY...
http://www.genetic.org/
About these children who comprised 2% of live births in the 1970s. They appeared to be girls at birth, but developed muscles, testes, and a penis at puberty.
http://www.usrf.org/news/010308-guevedoces.html
Includes such bitterly funny entries as "Ambiguous Genitalia: Genitalia that refuse to declare their sex to doctors--no doubt on the principle that under interrogation by the ...
http://www.sexuality.org/l/transgen/intvoca.html
Why it happens, what it is, what to do; see photos of hypospadias and contact others with it. Discusses androgen insensitivity, testicular feminization syndrome, development, and e...
http://www.the-penis.com/hypospadias.html
Information and support for intersexuals and parents of intersexuals. Articles on genital surgery, gender orientation, sexual identity, and message board.
http://www.healthyplace.com/communities/gender/intersexuals/
The biology of sex is being hotly debated, as parents, doctors and researchers reevaluate what it means to be male and female. This is an article about 'gender reinforcement' surge...
http://www.salon.com/health/feature/1999/04/05/sex_police/
UK-based organisation that aims to increase the public/government profile of genetic conditions. The AIS Support Group (UK) is affiliated to GIG.
http://www.gig.org.uk
A long article by Emily Nussbaum in the current issue of Lingua Franca details the rise of the increasingly successful intersex social justice movement, its alliances with humanis...
http://www.isna.org/pr/pr4-29-99.html
Contains support, information on hormone replacement therapy for folks with Turner's, health issues for folks with TS, and personal stories.
http://www.tss.org.uk/
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