{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,4]],"date-time":"2026-04-04T08:57:04Z","timestamp":1775293024548,"version":"3.50.1"},"reference-count":17,"publisher":"Wiley","issue":"2","license":[{"start":{"date-parts":[[2005,6,3]],"date-time":"2005-06-03T00:00:00Z","timestamp":1117756800000},"content-version":"vor","delay-in-days":5846,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Am. J. Med. Genet."],"published-print":{"date-parts":[[1989,6]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>We report an Arab Bedouin family including four males with uterine hernia syndrome. All had a male chromosome constitution and phenotype, inguinal herniae, cryptochidism, and persistence of M\u00fcllerian derivatives. Histopathological studies confirmed the presence of both testicular tissue and M\u00fcllerian derivatives. The presence of two affected brothers and two affected maternal uncles suggests X\u2010linked inheritance. Autosomal recessive determination with male sex limitation is also a possibility based on parental consanguinity in one sibship.<\/jats:p>","DOI":"10.1002\/ajmg.1320330208","type":"journal-article","created":{"date-parts":[[2005,6,12]],"date-time":"2005-06-12T03:02:45Z","timestamp":1118545365000},"page":"180-181","source":"Crossref","is-referenced-by-count":20,"title":["Familial uterine hernia syndrome: Report of an Arab family with four affected males"],"prefix":"10.1002","volume":"33","author":[{"given":"Kamal K.","family":"Naguib","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ahmad S.","family":"Teebi","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Talaat I.","family":"Farag","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Sadika A.","family":"Al\u2010Awadi","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Mohammed Y.","family":"El\u2010Khalifa","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"El\u2010Sayed","family":"Mahfouz","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2005,6,3]]},"reference":[{"key":"e_1_2_1_2_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1399-0004.1985.tb00236.x"},{"key":"e_1_2_1_3_1","doi-asserted-by":"publisher","DOI":"10.1136\/bmj.1.5856.771"},{"key":"e_1_2_1_4_1","doi-asserted-by":"publisher","DOI":"10.1159\/000132332"},{"key":"e_1_2_1_5_1","first-page":"249","article-title":"Male pseudohermaphroditism in two brothers","volume":"61","author":"David L","year":"1972","journal-title":"Acta Paediatr Scand"},{"key":"e_1_2_1_6_1","first-page":"343","article-title":"Male pseudohermaphroditism with internal bisexual genitals (A report on two brothers)","volume":"7","author":"Guell\u2010Gonzalez JR","year":"1970","journal-title":"Rev Roumaine Endocrinol"},{"key":"e_1_2_1_7_1","doi-asserted-by":"publisher","DOI":"10.1210\/jcem-32-3-404"},{"key":"e_1_2_1_8_1","doi-asserted-by":"publisher","DOI":"10.1210\/endo-93-4-829"},{"key":"e_1_2_1_9_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1365-2265.1986.tb01699.x"},{"key":"e_1_2_1_10_1","doi-asserted-by":"publisher","DOI":"10.1152\/physrev.1986.66.4.1038"},{"issue":"2","key":"e_1_2_1_11_1","first-page":"59","article-title":"The anti\u2010M\u00fcllerian hormone","author":"Josso N","year":"1977","journal-title":"BD:OAD"},{"key":"e_1_2_1_12_1","first-page":"231","article-title":"Hernia uteri inguinalis beim Manne","volume":"83","author":"Nilson O","year":"1939","journal-title":"Acta Chir Scand"},{"key":"e_1_2_1_13_1","first-page":"147","article-title":"Anti\u2010M\u00fcllerian hormone: Estimation of molecular weight by gel filtration","volume":"25","author":"Picard Y","year":"1976","journal-title":"Biomedicine"},{"key":"e_1_2_1_14_1","doi-asserted-by":"publisher","DOI":"10.1073\/pnas.83.15.5464"},{"key":"e_1_2_1_15_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1464-410X.1985.tb05864.x"},{"key":"e_1_2_1_16_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0022-5347(17)59242-3"},{"key":"e_1_2_1_17_1","doi-asserted-by":"publisher","DOI":"10.1042\/bj1500191"},{"key":"e_1_2_1_18_1","doi-asserted-by":"crossref","first-page":"797","DOI":"10.1542\/peds.61.5.797","article-title":"Persistent M\u00fcllerian duct syndrome in male identical twins","volume":"61","author":"Weiss EB","year":"1978","journal-title":"Pediatrics"}],"container-title":["American Journal of Medical Genetics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1002%2Fajmg.1320330208","content-type":"unspecified","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1002\/ajmg.1320330208","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,10,22]],"date-time":"2023-10-22T03:26:24Z","timestamp":1697945184000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/ajmg.1320330208"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1989,6]]},"references-count":17,"journal-issue":{"issue":"2","published-print":{"date-parts":[[1989,6]]}},"alternative-id":["10.1002\/ajmg.1320330208"],"URL":"https:\/\/doi.org\/10.1002\/ajmg.1320330208","archive":["Portico"],"relation":{},"ISSN":["0148-7299","1096-8628"],"issn-type":[{"value":"0148-7299","type":"print"},{"value":"1096-8628","type":"electronic"}],"subject":[],"published":{"date-parts":[[1989,6]]}}}