[1]
AIS (Androgen Insensitivity Syndrome) Support Group: http://www.aissg.org/.
[2]
Bhartiya, D. et al. 2013. Ovarian stem cells: absence of evidence is not evidence of absence. Journal of Ovarian Research. 6, 1 (2013). DOI:https://doi.org/10.1186/1757-2215-6-65.
[3]
Blackless, M. et al. 2000. How sexually dimorphic are we? Review and synthesis. American Journal of Human Biology. 12, 2 (2000), 151–166. DOI:https://doi.org/10.1002/(SICI)1520-6300(200003/04)12:2<151::AID-AJHB1>3.0.CO;2-F.
[4]
Brain, C.E. et al. 2010. Holistic management of DSD. Best Practice & Research Clinical Endocrinology & Metabolism. 24, 2 (Apr. 2010), 335–354. DOI:https://doi.org/10.1016/j.beem.2010.01.006.
[5]
Bukovsky, A. 2005. Can ovarian infertility be treated with bone marrow- or ovary-derived germ cells? Reproductive Biology and Endocrinology. 3, 1 (2005). DOI:https://doi.org/10.1186/1477-7827-3-36.
[6]
Bukovsky, A. 2011. Ovarian Stem Cell Niche and Follicular Renewal in Mammals. The Anatomical Record: Advances in Integrative Anatomy and Evolutionary Biology. 294, 8 (Aug. 2011), 1284–1306. DOI:https://doi.org/10.1002/ar.21422.
[7]
Creighton, S.M. et al. 2001. Objective cosmetic and anatomical outcomes at adolescence of feminising surgery for ambiguous genitalia done in childhood. The Lancet. 358, 9276 (Jul. 2001), 124–125. DOI:https://doi.org/10.1016/S0140-6736(01)05343-0.
[8]
Dean, C. and Pegington, J. 1996. Core anatomy for students: Volume 2: The thorax, abdomen, pelvis and perineum. W.B. Saunders.
[9]
Deans, R. et al. 2010. Management of Vaginal Hypoplasia in Disorders of Sexual Development: Surgical and Non-Surgical Options. Sexual Development. 4, 4–5 (2010), 292–299. DOI:https://doi.org/10.1159/000316231.
[10]
dsd families: http://www.dsdfamilies.org/.
[11]
Eggan, K. et al. 2006. Ovulated oocytes in adult mice derive from non-circulating germ cells. Nature. 441, 7097 (Jun. 2006), 1109–1114. DOI:https://doi.org/10.1038/nature04929.
[12]
Eppig, J. 2001. Oocyte control of ovarian follicular development and function in mammals. Reproduction. 122, 6 (Dec. 2001), 829–838. DOI:https://doi.org/10.1530/rep.0.1220829.
[13]
Fakih, M.H. 2015. The AUGMENTSM Treatment: Physician Reported Outcomes of the Initial Global Patient Experience. Journal of Fertilization: In Vitro - IVF-Worldwide, Reproductive Medicine, Genetics & Stem Cell Biology. 03, 03 (2015). DOI:https://doi.org/10.4172/2375-4508.1000154.
[14]
Hughes, I.A. 2005. Consensus statement on management of intersex disorders. Archives of Disease in Childhood. 91, 7 (Jun. 2005), 554–563. DOI:https://doi.org/10.1136/adc.2006.098319.
[15]
Johnson, J. et al. 2004. Germline stem cells and follicular renewal in the postnatal mammalian ovary. Nature. 428, 6979 (Mar. 2004), 145–150.
[16]
Johnson, J. et al. 2004. Germline stem cells and follicular renewal in the postnatal mammalian ovary. Nature. 428, 6979 (Mar. 2004), 145–150. DOI:https://doi.org/10.1038/nature02316.
[17]
Johnson, J. et al. 29AD. Oocyte Generation in Adult Mammalian Ovaries by Putative Germ Cells in Bone Marrow and Peripheral Blood. Oocyte Generation in Adult Mammalian Ovaries by Putative Germ Cells in Bone Marrow and Peripheral Blood. 122, 2 (29AD), 303–315.
[18]
Johnson, M.H. and Johnson, M.H. 2013. Essential reproduction. Wiley-Blackwell.
[19]
Kidder, G. and Mhawi, A. 2002. Gap junctions and ovarian folliculogenesis. Reproduction. 123, 5 (May 2002), 613–620. DOI:https://doi.org/10.1530/rep.0.1230613.
[20]
Liao, L.-M. et al. 2010. Service users’ experiences of obtaining and giving information about disorders of sex development. BJOG: An International Journal of Obstetrics & Gynaecology. 117, 2 (Jan. 2010), 193–199. DOI:https://doi.org/10.1111/j.1471-0528.2009.02385.x.
[21]
Matzuk, M.M. 2002. Intercellular Communication in the Mammalian Ovary: Oocytes Carry the Conversation. Science. 296, 5576 (Jun. 2002), 2178–2180. DOI:https://doi.org/10.1126/science.1071965.
[22]
Silvestris, E. et al. 2015. Perspective in infertility: the ovarian stem cells. Journal of Ovarian Research. 8, 1 (Dec. 2015). DOI:https://doi.org/10.1186/s13048-015-0184-9.
[23]
Sriraman, K. et al. 2015. Mouse Ovarian Very Small Embryonic-Like Stem Cells Resist Chemotherapy and Retain Ability to Initiate Oocyte-Specific Differentiation. Reproductive Sciences. 22, 7 (Jul. 2015), 884–903. DOI:https://doi.org/10.1177/1933719115576727.
[24]
Tilly, J.L. and Johnson, J. 2007. Recent Arguments Against Germ Cell Renewal in the Adult Human Ovary: Is an Absence of Marker Gene Expression Really Acceptable Evidence of an Absence of Oogenesis? Cell Cycle. 6, 8 (Apr. 2007), 879–883. DOI:https://doi.org/10.4161/cc.6.8.4185.
[25]
Tilly, J.L. and Johnson, J. 2007. Recent Arguments Against Germ Cell Renewal in the Adult Human Ovary: Is an Absence of Marker Gene Expression Really Acceptable Evidence of an Absence of Oogenesis? Cell Cycle. 6, 8 (Apr. 2007), 879–883. DOI:https://doi.org/10.4161/cc.6.8.4185.
[26]
Truman, A.M. et al. 2016. Ovarian regeneration: The potential for stem cell contribution in the postnatal ovary to sustained endocrine function. Molecular and Cellular Endocrinology. (Oct. 2016). DOI:https://doi.org/10.1016/j.mce.2016.10.012.
[27]
Veitia, R.A. et al. 2007. Recovery of Female Fertility After Chemotherapy, Irradiation, and Bone Marrow Allograft: Further Evidence Against Massive Oocyte Regeneration by Bone Marrow-Derived Germline Stem Cells. Stem Cells. 25, 5 (May 2007), 1334–1335. DOI:https://doi.org/10.1634/stemcells.2006-0770.
[28]
White, Y.A.R. et al. 2012. Oocyte formation by mitotically active germ cells purified from ovaries of reproductive-age women. Nature Medicine. 18, 3 (Feb. 2012), 413–421. DOI:https://doi.org/10.1038/nm.2669.
[29]
White, Y.A.R. et al. 2012. Oocyte formation by mitotically active germ cells purified from ovaries of reproductive-age women. Nature Medicine. 18, 3 (Feb. 2012), 413–421. DOI:https://doi.org/10.1038/nm.2669.
[30]
Zou, K. et al. 2009. Production of offspring from a germline stem cell line derived from neonatal ovaries. Nature Cell Biology. 11, 5 (May 2009), 631–636. DOI:https://doi.org/10.1038/ncb1869.
[31]
Menopause.
[32]
Sexual development: genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation.