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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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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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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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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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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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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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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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Research advances on medical genetics in China in 2015

Yíchuán, 2016-05, Vol.38 (5), p.363

2016

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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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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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Multiplex quantitative PCR detection for female carrier in an X-linked ichthyosis family

Zhong hua yi xue za zhi, 2008-12, Vol.88 (46), p.3246-3249

2008

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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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Mutation screening of 20 candidate genes located in chromo-some 5q31-5q32 for DFNA52 locus

Yíchuán, 2009-01, Vol.31 (1), p.43

2009

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Identification of the origin of marker chromosome by comparative genomic hybridization

Zhong nan da xue xue bao. Journal of Central South University. Yi xue ban, 2007-04, Vol.32 (2), p.264-267

2007

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Mapping of pathogenic genes in two families with autosomal dominant ichthyosis vulgaris

Yíchuán, 2008-07, Vol.30 (7), p.843

2008

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Research progress in nonsyndromic sensorineural hearing loss associated genes

Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery, 2005-08, Vol.40 (8), p.633

2005

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Preimplantation genetic diagnosis of Duchenne muscular dystrophy by single cell triplex PCR

Zhong nan da xue xue bao. Journal of Central South University. Yi xue ban, 2007-04, Vol.32 (2), p.246-251

2007

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Prenatal diagnosis and genetic counseling

Chung-hua fu chʿan kʿo tsa chih, 2003-08, Vol.38 (8), p.474-477

2003

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Prenatal diagnosis of prelingual deafness by determination of SLC26A4 gene mutation

Chung-hua fu chʿan kʿo tsa chih, 2005-09, Vol.40 (9), p.591-594

2005

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

Etiology and diagnosis of intellectual disability

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

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

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

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

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

Research advances on medical genetics in China in 2015

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

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

Multiplex quantitative PCR detection for female carrier in an X-linked ichthyosis family

First report of HGD mutations in a Chinese with alkaptonuria

Mutation screening of 20 candidate genes located in chromo-some 5q31-5q32 for DFNA52 locus

Identification of the origin of marker chromosome by comparative genomic hybridization

Mapping of pathogenic genes in two families with autosomal dominant ichthyosis vulgaris

Research progress in nonsyndromic sensorineural hearing loss associated genes

Preimplantation genetic diagnosis of Duchenne muscular dystrophy by single cell triplex PCR

Prenatal diagnosis and genetic counseling

Prenatal diagnosis of prelingual deafness by determination of SLC26A4 gene mutation

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