Khomsak Srilanchakon, V. Supornsilchai, K. Suphapeetiporn
{"title":"一种新的FAM111A基因突变在肯尼-卡菲综合征2型儿童中表现为矮个子、髓质狭窄和甲状旁腺功能减退","authors":"Khomsak Srilanchakon, V. Supornsilchai, K. Suphapeetiporn","doi":"10.1530/boneabs.7.p119","DOIUrl":null,"url":null,"abstract":"","PeriodicalId":9160,"journal":{"name":"Bone Abstracts","volume":"43 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-07-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A novel mutation in FAM111A gene in child with Kenny-Caffey syndrome type 2 presenting with short statue, medullary stenosis and hypoparathyroidism\",\"authors\":\"Khomsak Srilanchakon, V. Supornsilchai, K. Suphapeetiporn\",\"doi\":\"10.1530/boneabs.7.p119\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"\",\"PeriodicalId\":9160,\"journal\":{\"name\":\"Bone Abstracts\",\"volume\":\"43 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-07-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Bone Abstracts\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1530/boneabs.7.p119\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bone Abstracts","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1530/boneabs.7.p119","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}