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Author:( Yueqiu DU)

1.The reliability and validity of the Chinese version of dynamic occupational therapy cognitive assessment for children

Yueqiu DU ; Zhihai LV ; Liping WANG ; Liling ZHU ; Zhimei JIANG

Chinese Journal of Physical Medicine and Rehabilitation 2011;33(8):583-586

2.Validity of Dynamic Occupational Therapy Cognitive Assessment for Children on Cognitive Function of Children with Cerebral Palsy

Zhihai LV ; Zhimei JIANG ; Yueqiu DU ; Lanmin GUO ; Beibei KANG ; Shiling ZHANG

Chinese Journal of Rehabilitation Theory and Practice 2013;19(6):553-555

3.Pre-conception carrier screening for 21 inherited metabolic diseases in a Chinese population.

Xilin XU ; Wenbin HE ; Ying WANG ; Fei GONG ; Guangxiu LU ; Ge LIN ; Yueqiu TAN ; Juan DU

Chinese Journal of Medical Genetics 2022;39(3):269-275

4.Analysis of a novel mutation of AR gene in a patient featuring mild androgen insensitivity syndrome.

Yanan ZHANG ; Wen LI ; Juan DU ; Wanglong CAO ; Guangxiu LU ; Yueqiu TAN

Chinese Journal of Medical Genetics 2014;31(2):219-222

5.Study of a family with epidermolysis bullosa simplex resulting from a novel mutation of KRT14 gene.

Lanlan MENG ; Juan DU ; Wen LI ; Guangxiu LU ; Yueqiu TAN

Chinese Journal of Medical Genetics 2017;34(4):504-508

6.Karyotyping and analysis of 5α -reductase-2 gene mutation in 25 patients with hypospadias.

Shimin YUAN ; Changgao ZHONG ; Xiurong LI ; Juan DU ; Wen LI ; Guangxiu LU ; Yueqiu TAN

Chinese Journal of Medical Genetics 2017;34(2):159-163

7.Analysis of FMR1 gene CGG repeats among patients with diminished ovarian reserve.

Wenbin HE ; Weilin TANG ; Yi LIAO ; Wen LI ; Fei GONG ; Guangxiu LU ; Ge LIN ; Juan DU ; Yueqiu TAN

Chinese Journal of Medical Genetics 2021;38(4):343-346

8.Analysis and prenatal diagnosis of FMR1 gene mutations among patients with unexplained mental retardation.

Shikun LUO ; Wenbin HE ; Yi LIAO ; Weilin TANG ; Xiurong LI ; Liang HU ; Juan DU ; Qianjun ZHANG ; Yueqiu TAN ; Ge LIN ; Wen LI

Chinese Journal of Medical Genetics 2021;38(5):439-445

9.Genetic study on a consanguineous Chinese family with premature ovarian insufficiency caused by a missense mutation of PSMC3IP gene

Guiquan MENG ; Lanlan MENG ; Juan DU ; Guangxiu LU ; Yueqiu TAN ; Ge LIN ; Wenbin HE

Journal of Chinese Physician 2021;23(9):1286-1289

10.Analysis of FOXL2 gene mutations in 5 families affected with blepharophimosis, ptosis and epicanthus inversus syndrome.

Xiaowen YANG ; Wen LI ; Juan DU ; Shimin YUAN ; Wenbin HE ; Qianjun ZHANG ; Changgao ZHONG ; Guangxiu LU ; Yueqiu TAN

Chinese Journal of Medical Genetics 2017;34(3):342-346

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