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DNA analysis using X chromosome sequences from the pericentromeric region and from distal X<jats:sub>q<\/jats:sub> suggests that the patient is homozygous at the fra(X) locus due to maternal nondisjunction during meiosis II.<\/jats:p>","DOI":"10.1002\/ajmg.1320380260","type":"journal-article","created":{"date-parts":[[2005,6,12]],"date-time":"2005-06-12T04:09:12Z","timestamp":1118549352000},"page":"440-444","source":"Crossref","is-referenced-by-count":12,"title":["Origin of the supernumerary X chromosome in a patient with fragile X and Klinefelter syndrome"],"prefix":"10.1002","volume":"38","author":[{"given":"Kenneth G.","family":"Kupke","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A.","family":"Lee 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