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Genet."],"published-print":{"date-parts":[[1984,1]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>A review of 61 males with the fragile X positive form of the Martin Bell syndrome from 30 families seen in the past 4 years suggests that the number of lymphocytes with the fragile site on the X chromosome (fra(X)) in retarded males tends to be characteristic for the individual and similar to that found in other retarded males in the same family. The number of lymphocytes with fra(X) was not correlated with height, weight, occipitofrontal circumference, ear length or mean testicular volume in adults nor with age over the whole series.<\/jats:p>","DOI":"10.1002\/ajmg.1320170115","type":"journal-article","created":{"date-parts":[[2005,6,11]],"date-time":"2005-06-11T19:00:44Z","timestamp":1118516444000},"page":"241-252","source":"Crossref","is-referenced-by-count":26,"title":["The fragile X syndrome I: Familial variation in the proportion of lymphocytes with the fragile site in males"],"prefix":"10.1002","volume":"17","author":[{"given":"D.","family":"Soudek","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M. W.","family":"Partington","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"J. 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The fragile X syndrome II: preliminary data on growth and development.Amer J Med Genet(in press)."},{"key":"e_1_2_1_12_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.1320120211"},{"key":"e_1_2_1_13_1","first-page":"253","article-title":"Fragile X\u2010linked mental retardation: the Martin\u2010Bell syndrome","volume":"25","author":"Richards BW","year":"1981","journal-title":"J Ment Defic Res"},{"key":"e_1_2_1_14_1","doi-asserted-by":"publisher","DOI":"10.1007\/BF00569212"},{"key":"e_1_2_1_15_1","unstructured":"SoudekD PartingtonMW McGregorT(1981.Cytogenetic variation between families with fragile X disease. Abstracts of the Sixth International Congress of Human Genetics Jerusalem p251."},{"key":"e_1_2_1_16_1","doi-asserted-by":"publisher","DOI":"10.1007\/BF00289445"},{"key":"e_1_2_1_17_1","unstructured":"UchidaIA FreemanVCP JamroH PartingtonMW SoltanHC(1983). Additional evidence for fragile X activity in heterozygous carriers.Amer J Hum Genet(in press)."}],"container-title":["American Journal of Medical Genetics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1002%2Fajmg.1320170115","content-type":"unspecified","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1002\/ajmg.1320170115","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,10,19]],"date-time":"2023-10-19T19:40:12Z","timestamp":1697744412000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/ajmg.1320170115"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1984,1]]},"references-count":16,"journal-issue":{"issue":"1","published-print":{"date-parts":[[1984,1]]}},"alternative-id":["10.1002\/ajmg.1320170115"],"URL":"https:\/\/doi.org\/10.1002\/ajmg.1320170115","archive":["Portico"],"relation":{},"ISSN":["0148-7299","1096-8628"],"issn-type":[{"value":"0148-7299","type":"print"},{"value":"1096-8628","type":"electronic"}],"subject":[],"published":{"date-parts":[[1984,1]]}}}