Congenital hypothyroidism - Globe Thesis

Keyword [Congenital hypothyroidism] Result: 21 - 40 \| Page: 2 of 4
21.	Mutation Of TRβ And DUOXA1 Gene In Children With Congenital Hypothyroidism
22.	Screening Of TTF2 (FOXE1) Gene Mutation In Children With Congenital Hypothyroidism And Hypothyroidism
23.	Study Of Newborn Screening In Zheijiang Province From1999to2010
24.	Function Study Of NKX2-1 Gene Mutation, Which Caused Congenital Hypothyroidism And Central Nervous System Disorders
25.	Research On The Effect Of Maternal Thyroid Autoimmune Antibodies On The Development Of Their Offspring
26.	Gene Mutation Study Of Dual Oxidase 1(DUOX1) In Patients Of Congenital Hypothyroidism With Goiter
27.	Assessment Of Left Ventricular Longitudinal Systolic Function Of Congenital Hypothyroidism By Two-dimensional Speckle Tracking Imaging
28.	The Expression And DNA Methylation Of EphA5in The Brain Of Rat With Congenital Hypothyroidism
29.	A Study Of Gene Mutation In The Patients Of Congenital Hypothyroidism
30.	The Study Of Newborn Congenital Hypothyroidism Screening In SuZhou From 1999 To 2013
31.	Study On The Transgenic Rat Model Of Congenital Hypothyroidism Via CRISPR/cas9
32.	Analysis Of Congenital Hypothyroidism On Epidemiological Characteristics And The Therapeutic Effects In Shanxi Province
33.	Effects Of Congenital Hypothyroidism On Cardiac Development
34.	Study On DUOX1 Mutation Screening And Pathogenic Mechanism Of DUOX1/DUOXA1 Mutation In CH Patients With Goiter
35.	Screening And Research The DUOX2 Mutation In Patients With Congenital Hypothyroidism In Northwestern Region
36.	Screening And Research The TG Mutation In Patients With Congenital Hypothyroidism
37.	Genetic Screening Of Pathogetic Genes (TTF-1?TTF-2?NKX2.5?PAX8?TSHR And NIS) In Patients With Congenital Hypothyroidism
38.	The Data Analysis Of The Morbidity And Correlative Factors For Newborn Congenital Hypothyroidism Screening In HengYang From 2013 To 2015
39.	Study On Mutations Of Nicotinamide Nucleotide Transhydrolase In Patients With Congenital Hypothyroidism And Thyroid Dysplasia
40.	Study On GLI-Similar3 Mutations In Patients With Congenital Hypothyroidism
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