M S Bhate, P E Robertson, E V Davison, J A Brummitt
{"title":"伴有甲状腺功能减退的Prader Willi综合征。","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":"{\"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}","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}
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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