Strong Genotype-Phenotype Correlation in Pendred Syndrome Allows Reduced Endocrine Follow-up in Suitable Patients

被引：0
|
作者：
Soh, Lip Min [1 ]
Druce, Maralyn [1 ]
Grossman, Ashley B. [2 ]
Differ, Ann-Marie [3 ]
Rajput, Liala [4 ]
Bitner-Glindzicz, Maria [5 ]
Korbonits, Marta [6 ]
机构：
[1] Queen Mary Univ London, Barts & London Sch Med, William Harvey Res Inst, Ctr Endocrinol, London, England
[2] Oxford Ctr Diabet Endocrinol & Metab, Oxford, England
[3] Great Ormond St Hosp Children NHS Fdn Trust, North East Thames Reg Genet Serv Lab, London, England
[4] Great Ormond St Hosp Children NHS Fdn Trust, Cochlear Implant Dept, London, England
[5] Great Ormond St Hosp Children NHS Fdn Trust, Clin Genet Unit, London, England
[6] Queen Mary Univ London, Barts & London Sch Med, William Harvey Res Inst, London, England
来源：
ENDOCRINE REVIEWS | 2014年 / 35卷 / 03期
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D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
OR29-5
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收藏
页数：3
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