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SUN-363 Hypophosphatemia Gene Panel Sponsored Program: A High Yield Of Molecular Diagnoses from Clinically Confirmed XLH and Suspected XLH/ Genetic Hypophosphatemia

机译：Sun-363次磷血症基因面板赞助计划：从临床证实的XLH和可疑的XLH /遗传次磷血症的分子诊断的高产

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Nicole Miller; Kathryn Dahir; Daniel Beltran; Scott J Eisenbeis; Prameela Ramesan; Eric T Rush; Soodabeh Sarafrazi; Rebecca Truty; Britt Johnson;
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1. X-Linked Hypophosphatemia (XLH): New Knowledge for Nurses Regarding Genetics, Pathophysiology and Clinical Presentation [J] . Couto Isabel, Hart Marian, Olear Elizabeth, Journal of pediatric nursing . 2019,第期

机译：X-Linked次磷血症（XLH）：关于遗传学，病理生理学和临床介绍的护士新知识
2. High iFGF23 level despite hypophosphatemia is one of the clinical indicators to make diagnosis of XLH [J] . Junko Miyamoto Igaki, Makoto Yamada, Yuji Yamazaki, Endocrine journal . 2011,第8期

机译：尽管存在低磷血症，但高iFGF23水平是诊断XLH的临床指标之一
3. High iFGF23 level despite hypophosphatemia is one of the clinical indicators to make diagnosis of XLH [J] . Daisuke Ariyasu, Eri Suzuki, Hisashi Hasegawa, Endocrine journal . 2011,第8期

机译：尽管存在低磷血症，但iFGF23水平仍很高，是诊断XLH的临床指标之一
4. Factor VII Deficiency:Clinical Manifestation and Molecular Genetics of 718 Subjects with FVII Gene Mutations [C] . F. H. Herrmann, K. Wulff, G. Auerswald, Hemophilia Symposium . 2008

机译：因子vii缺乏：718个受试者的临床表现与FVII基因突变的临床表现和分子遗传学
5. Imaging Genetics and Biomarker Variations of Clinically Diagnosed Alzheimer’s Disease [D] . ?Stage, Eddie Carl, Jr. 2020

机译：临床诊断的阿尔茨海默病的成像遗传学和生物标志物变异
6. SUN-363 Hypophosphatemia Gene Panel Sponsored Program: A High Yield Of Molecular Diagnoses from Clinically Confirmed XLH and Suspected XLH/ Genetic Hypophosphatemia [O] . Nicole Miller, Kathryn Dahir, Daniel Beltran, 2020

机译：Sun-363次磷血症基因面板赞助计划：从临床证实的XLH和可疑的XLH /遗传次磷血症的分子诊断的高产
7. SUN-356 Burosumab Resulted in Greater Clinical Improvements Compared with Higher-dose Conventional Therapy in Children with X-linked Hypophosphatemia (XLH) [O] . Erik A Imel, Angel Chen, Ting Chang, 2020

机译：Sun-356 Burosumab导致与X型次磷血症儿童的较高剂量常规治疗相比，临床改善更大的临床改善（XLH）

SUN-363 Hypophosphatemia Gene Panel Sponsored Program: A High Yield Of Molecular Diagnoses from Clinically Confirmed XLH and Suspected XLH/ Genetic Hypophosphatemia

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