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Genet."],"published-print":{"date-parts":[[1983,7]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Recently we evaluated a Saudi Arabian family in which a severely affected male and a more mildly affected set of monozygotic (MZ) female twins had manifestations of the B\u00f6rjeson\u2010Forssman\u2010Lehmann syndrome including short stature, hypotonia, mental deficiency, coarse facial appearance with a prominent brow\u2010ridge, and large ears. We present clinical, radiographic, electroencephalographic, and endocrinologic data to further delineate this condition and set forth the manifestations of two normal, presumably heterozygous, females.<\/jats:p>","DOI":"10.1002\/ajmg.1320150311","type":"journal-article","created":{"date-parts":[[2005,6,11]],"date-time":"2005-06-11T18:52:39Z","timestamp":1118515959000},"page":"457-468","source":"Crossref","is-referenced-by-count":23,"title":["The B\u00f6rjeson\u2010Forssman\u2010Lehmann syndrome"],"prefix":"10.1002","volume":"15","author":[{"given":"Luther K.","family":"Robinson","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kenneth Lyons","family":"Jones","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Floyd","family":"Culler","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"William L.","family":"Nyhan","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Nadia","family":"Sakati","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kenneth Lee","family":"Jones","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"John M.","family":"Opitz","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2005,6,2]]},"reference":[{"key":"e_1_2_1_2_1","doi-asserted-by":"publisher","DOI":"10.1016\/0039-128X(76)90108-2"},{"key":"e_1_2_1_3_1","first-page":"125","article-title":"The B\u00f6rjeson\u2010Forssman\u2010Lehmann syndrome","volume":"9","author":"Baar HS","year":"1965","journal-title":"J Ment Defic Res"},{"key":"e_1_2_1_4_1","doi-asserted-by":"publisher","DOI":"10.2337\/diab.21.10.1013"},{"key":"e_1_2_1_5_1","doi-asserted-by":"crossref","first-page":"12","DOI":"10.1111\/j.0954-6820.1962.tb04162.x","article-title":"An X\u2010linked recessively inherited syndrome characterized by grave mental deficiency, epilepsy and endocrine disorder","volume":"171","author":"B\u00f6rjeson M","year":"1962","journal-title":"Acta Med Scand"},{"key":"e_1_2_1_6_1","first-page":"188","volume-title":"Combination of idiocy, epilepsy, hypogonadism, dwarfism, hypometabolism, and morphologic peculiarities inherited as an X\u2010linked recessive syndrome. 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