{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,2]],"date-time":"2026-10-02T23:29:31Z","timestamp":1790983771545,"version":"4.1.0"},"reference-count":8,"publisher":"BMJ","issue":"7","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Med Genet"],"published-print":{"date-parts":[[1987,7]]},"abstract":"<jats:p>A boy with the cutaneous lesions of incontinentia pigmenti is described. Chromosomal analysis revealed the 47,XXY karyotype of Klinefelter's syndrome. Since incontinentia pigmenti trait is usually lethal in males, the possibility of the second X chromosome protecting against fetal death is discussed.<\/jats:p>","DOI":"10.1136\/jmg.24.7.439","type":"journal-article","created":{"date-parts":[[2008,11,10]],"date-time":"2008-11-10T15:09:16Z","timestamp":1226329756000},"page":"439-441","source":"Crossref","is-referenced-by-count":43,"title":["Incontinentia pigmenti in a boy with Klinefelter's syndrome."],"prefix":"10.1136","volume":"24","author":[{"given":"A D","family":"Ormerod","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"M I","family":"White","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"E","family":"McKay","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"A W","family":"Johnston","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"239","published-online":{"date-parts":[[1987,7,1]]},"reference":[{"key":"ref_1","doi-asserted-by":"crossref","first-page":"177","DOI":"10.1111\/j.1399-0004.1983.tb02235.x","article-title":"The half chromatid mutation model and bidirectional mutation in incontinentia pigmenti","volume":"24","author":"Hecht, F.; Hecht, B.K.","year":"1983","unstructured":"Hecht F, Hecht BK. 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Two cases of X\/autosome translocation in females with incontinentia pigmenti. Hum Genet 1985;71:231-4.","journal-title":"Hum Genet"},{"key":"ref_8","doi-asserted-by":"crossref","first-page":"238","DOI":"10.1111\/j.1399-0004.1985.tb00392.x","article-title":"X inactivation patterns in two syndromes with probable X-linked dominant male lethal inheritance","volume":"28","author":"Wieacker, P.; Zimmer, J.; Ropers, H.","year":"1985","unstructured":"Wieacker P, Zimmer J, Ropers H. X inactivation patterns in two syndromes with probable X-linked dominant male lethal inheritance. 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