M S Bhate, P E Robertson, E V Davison, J A Brummitt
{"title":"Prader Willi syndrome with hypothyroidism.","authors":"M S Bhate, P E Robertson, E V Davison, J A Brummitt","doi":"10.1111/j.1365-2788.1989.tb01471.x","DOIUrl":null,"url":null,"abstract":"<p><p>A case of Prader Willi Syndrome who suffered from hypothyroidism is described. This patient on cytogenetic examination was found to have Mosaic 46,XX/46,XX,del(15)(q11.1q11.2) karyotype.</p>","PeriodicalId":76014,"journal":{"name":"Journal of mental deficiency research","volume":"33 ( Pt 3) ","pages":"235-44"},"PeriodicalIF":0.0000,"publicationDate":"1989-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/j.1365-2788.1989.tb01471.x","citationCount":"10","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of mental deficiency research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1111/j.1365-2788.1989.tb01471.x","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 10
Abstract
A case of Prader Willi Syndrome who suffered from hypothyroidism is described. This patient on cytogenetic examination was found to have Mosaic 46,XX/46,XX,del(15)(q11.1q11.2) karyotype.
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