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Robust Adaptive Tracking Control for Manipulators Based on a TSK Fuzzy Cerebellar Model Articulation Controller

IEEE access, 2018-01, Vol.6, p.1670-1679

2018

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Novel SIL1 nonstop mutation in a Chinese consanguineous family with Marinesco-Sjögren syndrome and Dandy-Walker syndrome

Clinica chimica acta, 2016-07, Vol.458, p.1-4

2016

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Pallister-Killian syndrome： meiosis Ⅱ non-disjunction may be the first step in the formation of isochromosome 12p

Chinese medical journal, 2010-12, Vol.123 (23), p.3482-3485

2010

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Single-cell RNA sequencing reveals distinct gene expression patterns in glucose metabolism of human preimplantation embryos

Reproduction fertility and development, 2019-01, Vol.31 (2), p.237

2019

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Molecular medicine of fragile X syndrome: based on known molecular mechanisms

World journal of pediatrics : WJP, 2016-02, Vol.12 (1), p.19-27

2016

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Etiology and diagnosis of intellectual disability

Zhongguo dang dai er ke za zhi, 2015-06, Vol.17 (6), p.543

2015

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First report of HGD mutations in a Chinese with alkaptonuria

Gene, 2013-04, Vol.518 (2), p.467-469

2013

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Analysis of PAX6 gene in a Chinese aniridia family

Chinese medical journal, 2006-08, Vol.119 (16), p.1400-1402

2006

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Confirmation and refinement of a genetic locus of congenital motor nystagmus in xq26.3-q27.1 in a Chinese family

Human genetics, 2005, Vol.116 (1-2), p.128-131

2005

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Rapid genetic diagnosis and prenatal diagnosis of spinal muscular atrophy by denaturing high-performance liquid chromatography

Chinese medical journal, 2006-07, Vol.119 (14), p.1222-1225

2006

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Cornelia de Lange syndrome: report of a case and the review of literature on 17 cases

Zhonghua er ke za zhi, 2012-08, Vol.50 (8), p.606

2012

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Intracellular Distribution, Assembly and Effect of Disease‐associated Connexin 31 Mutants in HeLa Cells

Acta biochimica et biophysica Sinica, 2005-08, Vol.37 (8), p.547-554

2005

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A case of malonyl-CoA decarboxylase deficiency: clinical and genetic study

Zhongguo dang dai er ke za zhi, 2012-11, Vol.14 (11), p.879

2012

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Mutation analysis of EXT genes in two pedigrees with hereditary multiple exostoses

Zhonghua yi xue yi chuan xue za zhi, 2013-12, Vol.30 (6), p.641

2013

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Analysis of four fetuses with de novo chromosomal rearrangments using single nucleotide polymorphism microarray chips

Zhonghua yi xue yi chuan xue za zhi, 2012-12, Vol.29 (6), p.658

2012

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Effect of heat treatment on corrosion behavior of low pressure sand cast Mg-10Gd-3Y-0.5Zr alloys

China foundry, 2016-07, Vol.13 (4), p.276-283

2016

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Cx31 is assembled and trafficked to cell surface by ER-Golgi pathway and degraded by proteasomal or lysosomal pathways

Cell research, 2005-06, Vol.15 (6), p.455-464

2005

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Research on Energy-Saving Reconstruction Technology of Hospital Buildings Based on Measured Data

E3S web of conferences, 2023-01, Vol.423, p.2007

2023

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Identification of the Alternative Promoters of the KChIP4 Subfamily

Acta biochimica et biophysica Sinica, 2005-04, Vol.37 (4), p.241-247

2005

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Mutational screening of the SLC26A4 gene in patients with nonsyndromic hearing loss by denaturing high-performance liquid chromatography

Zhonghua yi xue yi chuan xue za zhi, 2009-02, Vol.26 (1), p.21

2009

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Rapid detection of the hot spot gene mutations in Chinese patients with nonsyndromic hearing loss by polymerase chain reaction-restrictive fragment length polymorphism

Zhonghua yi xue yi chuan xue za zhi, 2009-10, Vol.26 (5), p.518

2009

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Molecular analysis of IDS gene and prenatal diagnosis in a Chinese family with mucopolysaccharidosis type II

Zhonghua er ke za zhi, 2009-02, Vol.47 (2), p.109

2009

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Genetic diagnosis and prenatal diagnosis of Angelman syndrome

Zhonghua yi xue yi chuan xue za zhi, 2009-10, Vol.26 (5), p.511

2009

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Deletion and mutation analysis to FOXL2 in blepharophimosis-ptosis-epicanthus inversus syndrome

Chung-hua yen k'o tsa chih, 2010-06, Vol.46 (6), p.532

2010

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A susceptibility locus at chromosome 3p21 linked to familial nasopharyngeal carcinoma

Cancer research (Chicago, Ill.), 2004-03, Vol.64 (6), p.1972-1974

2004

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Robust Adaptive Tracking Control for Manipulators Based on a TSK Fuzzy Cerebellar Model Articulation Controller

Novel SIL1 nonstop mutation in a Chinese consanguineous family with Marinesco-Sjögren syndrome and Dandy-Walker syndrome

Pallister-Killian syndrome： meiosis Ⅱ non-disjunction may be the first step in the formation of isochromosome 12p

Single-cell RNA sequencing reveals distinct gene expression patterns in glucose metabolism of human preimplantation embryos

Molecular medicine of fragile X syndrome: based on known molecular mechanisms

Etiology and diagnosis of intellectual disability

First report of HGD mutations in a Chinese with alkaptonuria

Analysis of PAX6 gene in a Chinese aniridia family

Confirmation and refinement of a genetic locus of congenital motor nystagmus in xq26.3-q27.1 in a Chinese family

Rapid genetic diagnosis and prenatal diagnosis of spinal muscular atrophy by denaturing high-performance liquid chromatography

Cornelia de Lange syndrome: report of a case and the review of literature on 17 cases

Intracellular Distribution, Assembly and Effect of Disease‐associated Connexin 31 Mutants in HeLa Cells

A case of malonyl-CoA decarboxylase deficiency: clinical and genetic study

Mutation analysis of EXT genes in two pedigrees with hereditary multiple exostoses

Analysis of four fetuses with de novo chromosomal rearrangments using single nucleotide polymorphism microarray chips

Effect of heat treatment on corrosion behavior of low pressure sand cast Mg-10Gd-3Y-0.5Zr alloys

Cx31 is assembled and trafficked to cell surface by ER-Golgi pathway and degraded by proteasomal or lysosomal pathways

Research on Energy-Saving Reconstruction Technology of Hospital Buildings Based on Measured Data

Identification of the Alternative Promoters of the KChIP4 Subfamily

Mutational screening of the SLC26A4 gene in patients with nonsyndromic hearing loss by denaturing high-performance liquid chromatography

Rapid detection of the hot spot gene mutations in Chinese patients with nonsyndromic hearing loss by polymerase chain reaction-restrictive fragment length polymorphism

Molecular analysis of IDS gene and prenatal diagnosis in a Chinese family with mucopolysaccharidosis type II

Genetic diagnosis and prenatal diagnosis of Angelman syndrome

Deletion and mutation analysis to FOXL2 in blepharophimosis-ptosis-epicanthus inversus syndrome

A susceptibility locus at chromosome 3p21 linked to familial nasopharyngeal carcinoma

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