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Linkage analysis of susceptibility loci in 2 target chromosomes in pedigrees with paranoid schizophrenia and undifferentiated schizophrenia

Zhonghua yi xue yi chuan xue za zhi, 2011-06, Vol.28 (3), p.256

2011

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Alcohol consumption in relation to the incidence of atrial fibrillation in an elderly Chinese population

Journal of geriatric cardiology : JGC, 2022-01, Vol.19 (1), p.52-60

2022

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Biotoxicology and biodynamics of silica nanoparticle

Zhong nan da xue xue bao. Journal of Central South University. Yi xue ban, 2006-02, Vol.31 (1), p.6

2006

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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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IT15 gene analysis in two pedigrees of Huntington's disease

Yíchuán, 2006-11, Vol.28 (11), p.1345

2006

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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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Mutation analysis of keratin 9 gene in a pedigree with epidermolytic palmoplantar keratoderma

Zhonghua yi xue yi chuan xue za zhi, 2004-12, Vol.21 (6), p.570

2004

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Identification and clone of human Alzheimer's disease related gene nicastrin promoter

Zhong nan da xue xue bao. Journal of Central South University. Yi xue ban, 2006-02, Vol.31 (1), p.9-13

2006

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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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Biological characteristics and safety evaluation of endothelial progenitor cells from the umbilical cord blood

Zhong nan da xue xue bao. Journal of Central South University. Yi xue ban, 2007-06, Vol.32 (3), p.466-472

2007

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Azoospermia factor microdeletion on Y chromosome in patients with idiopathic azoospermia or severe oligozoospermia

Zhong nan da xue xue bao. Journal of Central South University. Yi xue ban, 2007-04, Vol.32 (2), p.241-245

2007

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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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A mutation 1633-26(C-->A) in EXT1 gene causes multiple exostoses

Zhonghua yi xue yi chuan xue za zhi, 2006-04, Vol.23 (2), p.147

2006

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Hotspot of the mutations of keratin 9 gene in a diffuse palmoplantar keratoderma family

Zhong nan da xue xue bao. Journal of Central South University. Yi xue ban, 2005-10, Vol.30 (5), p.521-524

2005

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Construction of middle fragment deletion mutant with improved gene splicing by overlap extension

Zhonghua yi xue yi chuan xue za zhi, 2004-02, Vol.21 (1), p.52

2004

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Novel mutation of Y271H in EXT1 gene causes multiple exostoses

Zhong nan da xue xue bao. Journal of Central South University. Yi xue ban, 2007-08, Vol.32 (4), p.546-550

2007

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Mutation screening of the dystrophin gene in 14 Chinese Duchenne/Becker muscular dystrophy patients without gross deletions

Zhonghua yi xue yi chuan xue za zhi, 2008-12, Vol.25 (6), p.633

2008

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Chromosome analysis and phenotype location analysis on a patient with the karyotype of 45, XX, -13/46, XX, r(13)/46, XX, r(13;13)/47, XX, 2r(13)(p13q32.3)

Zhonghua yi xue yi chuan xue za zhi, 2004-08, Vol.21 (4), p.392

2004

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Splicing site mutation of D19S418 in PRPF-31 gene and its phenotypic characters with autosomal dominant retinitis pigmentosa

Chung-hua yen k'o tsa chih, 2005-11, Vol.41 (11), p.1020

2005

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Rapid prenatal diagnosis of chromosome aneuploidies in 60 uncultured amniotic fluid samples by fluorescence in situ hybridization

Zhonghua yi xue yi chuan xue za zhi, 2008-10, Vol.25 (5), p.538

2008

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Confirmation of the extra small chromosome in abnormality karyotype by PCR and FISH

Zhong nan da xue xue bao. Journal of Central South University. Yi xue ban, 2005-12, Vol.30 (6), p.657-659

2005

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Genetic linkage analysis in localizing a gene of autosomal dominant familial dilated cardiomyopathy with conduction defect

Zhong nan da xue xue bao. Journal of Central South University. Yi xue ban, 2005-10, Vol.30 (5), p.510-514

2005

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Linkage analysis of susceptibility loci in 2 target chromosomes in pedigrees with paranoid schizophrenia and undifferentiated schizophrenia

Alcohol consumption in relation to the incidence of atrial fibrillation in an elderly Chinese population

Biotoxicology and biodynamics of silica nanoparticle

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

IT15 gene analysis in two pedigrees of Huntington's disease

Research progress in nonsyndromic sensorineural hearing loss associated genes

Mutation analysis of keratin 9 gene in a pedigree with epidermolytic palmoplantar keratoderma

Identification and clone of human Alzheimer's disease related gene nicastrin promoter

Prenatal diagnosis of prelingual deafness by determination of SLC26A4 gene mutation

Biological characteristics and safety evaluation of endothelial progenitor cells from the umbilical cord blood

Azoospermia factor microdeletion on Y chromosome in patients with idiopathic azoospermia or severe oligozoospermia

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

Prenatal diagnosis and genetic counseling

A mutation 1633-26(C-->A) in EXT1 gene causes multiple exostoses

Hotspot of the mutations of keratin 9 gene in a diffuse palmoplantar keratoderma family

Construction of middle fragment deletion mutant with improved gene splicing by overlap extension

Novel mutation of Y271H in EXT1 gene causes multiple exostoses

Mutation screening of the dystrophin gene in 14 Chinese Duchenne/Becker muscular dystrophy patients without gross deletions

Chromosome analysis and phenotype location analysis on a patient with the karyotype of 45, XX, -13/46, XX, r(13)/46, XX, r(13;13)/47, XX, 2r(13)(p13q32.3)

Splicing site mutation of D19S418 in PRPF-31 gene and its phenotypic characters with autosomal dominant retinitis pigmentosa

Rapid prenatal diagnosis of chromosome aneuploidies in 60 uncultured amniotic fluid samples by fluorescence in situ hybridization

Confirmation of the extra small chromosome in abnormality karyotype by PCR and FISH

Genetic linkage analysis in localizing a gene of autosomal dominant familial dilated cardiomyopathy with conduction defect

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