{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,13]],"date-time":"2026-08-13T20:33:14Z","timestamp":1786653194428,"version":"build-2736575974"},"reference-count":7,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"4","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Min Access Surg"],"published-print":{"date-parts":[[2015]]},"DOI":"10.4103\/0972-9941.158160","type":"journal-article","created":{"date-parts":[[2015,6,4]],"date-time":"2015-06-04T09:06:31Z","timestamp":1433408791000},"page":"273","source":"Crossref","is-referenced-by-count":4,"title":["Laparoscopic hysterectomy with bilateral orchidectomy for Persistent Mullerian duct syndrome with seminoma testes: Case report"],"prefix":"10.4103","volume":"11","author":[{"given":"Senthilnathan","family":"Palanisamy","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"NikunjD","family":"Patel","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"SandeepC","family":"Sabnis","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Nalankilli","family":"Palanisamy","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Anand","family":"Vijay","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Palanivelu","family":"Chinnusamy","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","reference":[{"key":"key-10.4103\/0972-9941.158160-1","unstructured":"Rappaport R, Forest MG. Disorders of sexual differentiation. In: Bertrand J, Rappaport R, Gizonenko PC, editors. Pediatric Endocrinology. Baltimore, Tokyo: Williams & Wilkins; 1993. p. 447-70."},{"key":"key-10.4103\/0972-9941.158160-2","first-page":"1269","volume-title":"A 27 base-pair deletion of the anti-m\u00fcllerian type II receptor gene is the most common cause of the persistent m\u00fcllerian duct syndrome","author":"Imbeaud","year":"1996","journal-title":"Hum Mol Genet"},{"key":"key-10.4103\/0972-9941.158160-3","first-page":"122","volume-title":"Persistent m\u00fcllerian duct syndrome with or without transverse testicular ectopia and testis tumours","author":"Berkmen","year":"1997","journal-title":"Br J Urol"},{"key":"key-10.4103\/0972-9941.158160-4","first-page":"1231","volume-title":"A case of clear cell adenocarcinoma of the m\u00fcllerian duct in persistent m\u00fcllerian duct syndrome : t0 he first reported case","author":"Shinmura","year":"2002","journal-title":"Am J Surg Pathol"},{"key":"key-10.4103\/0972-9941.158160-5","first-page":"e29","volume-title":"Uterine adenosarcoma in a boy with persistent m\u00fcllerian duct syndrome : f0 irst reported case","author":"Thiel","year":"2005","journal-title":"J Pediatr Surg"},{"key":"key-10.4103\/0972-9941.158160-6","first-page":"941","volume-title":"Surgical management of persistent m\u00fcllerian duct syndrome","author":"Vandersteen","year":"1997","journal-title":"Urology"},{"key":"key-10.4103\/0972-9941.158160-7","first-page":"61","volume-title":"Surgical and genetic aspects of persistent m\u00fcllerian duct syndrome","author":"Loeff","year":"1994","journal-title":"J Pediatr Surg"}],"container-title":["Journal of Minimal Access Surgery"],"original-title":[],"language":"en","deposited":{"date-parts":[[2026,8,13]],"date-time":"2026-08-13T19:33:13Z","timestamp":1786649593000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.ovid.com\/10.4103\/0972-9941.158160"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2015]]},"references-count":7,"journal-issue":{"issue":"4","published-print":{"date-parts":[[2015]]}},"alternative-id":["158160"],"URL":"https:\/\/doi.org\/10.4103\/0972-9941.158160","relation":{},"ISSN":["0972-9941"],"issn-type":[{"value":"0972-9941","type":"print"}],"subject":[],"published":{"date-parts":[[2015]]}}}