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Origin of the X-chromosome influences the development and treatment outcomes of Turner syndrome

PeerJ (San Francisco, CA), 2021-12, Vol.9, p.e12354-e12354, Article e12354

2021

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Clinical analysis and genetic diagnosis of three children with Isoleucine metabolic disorders due to variants of HSD17B10 and ACAT1 genes

Zhonghua yi xue yi chuan xue za zhi, 2024-05, Vol.41 (5), p.540

2024

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POLG Mutations Are Probably Rare in the Han Chinese Population

Chinese medical sciences journal, 2020-12, Vol.35 (4), p.350-356

2020

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Clinical characteristics and identification of novel CNOT1 variants in three unrelated Chinese families with Vissers-Bodmer Syndrome

Heliyon, 2024-02, Vol.10 (4), p.e26743-e26743, Article e26743

2024

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Compound heterozygous mutations of NDUFV1 identified in a child with mitochondrial complex I deficiency

Genes & Genomics, 2022, 44(6), , pp.691-698

2022

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Mutation analysis of two pedigrees with suspected oculocutaneous albinism

Zhonghua yi xue yi chuan xue za zhi, 2019-03, Vol.36 (3), p.212

2019

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A rising trend of gastric cardia cancer in Gansu Province of China

Cancer letters, 2008-09, Vol.269 (1), p.18-25

2008

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Case–control study of risk factors of myelodysplastic syndromes according to World Health Organization classification in a Chinese population

American journal of hematology, 2011-02, Vol.86 (2), p.163-169

2011

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Application of a Multiplex Ligation-Dependent Probe Amplification-Based Next-Generation Sequencing Approach for the Detection of Pathogenesis of Duchenne Muscular Dystrophy and Spinal Muscular Atrophy Caused by Copy Number Aberrations

Molecular neurobiology, 2024-01, Vol.61 (1), p.200-211

2024

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Adult precursor B lymphoblastic leukemia in Shanghai, China: characterization of phenotype, cytogenetics and outcome for 137 consecutive cases

International journal of hematology, 2009-05, Vol.89 (4), p.431-437

2009

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Prospective study of 174 de novo acute myelogenous leukemias according to the WHO classification: subtypes, cytogenetic features and FLT3 mutations

European journal of haematology, 2006-07, Vol.77 (1), p.35-45

2006

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Compound heterozygous mutations of NDUFV1 identified in a child with mitochondrial complex I deficiency

Genes & genomics, 2022-06, p.691-698

2022

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A multiplex ligation‑dependent probe amplification‑based next‑generation sequencing approach for the detection of copy number variations in the human genome

Molecular medicine reports, 2018-12, Vol.18 (6), p.5823-5833

2018

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Genetic mutational profiling analysis of T cell acute lymphoblastic leukemia reveal mutant FBXW7 as a prognostic indicator for inferior survival

Annals of hematology, 2015-11, Vol.94 (11), p.1817-1828

2015

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A study of two Chinese patients with tetrasomy and pentasomy 15q11q13 including Prader-Willi/Angelman syndrome critical region present with developmental delays and mental impairment

BMC medical genetics, 2013-01, Vol.14 (1), p.9-9, Article 9

2013

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HLA class II alleles may influence susceptibility to adult dermatomyositis and polymyositis in a Han Chinese population

BMC dermatology, 2014-06, Vol.14 (1), p.9-9, Article 9

2014

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WT1 mutations and single nucleotide polymorphism rs16754 analysis of patients with pediatric acute myeloid leukemia in a Chinese population

Leukemia & lymphoma, 2012-11, Vol.53 (11), p.2195-2204

2012

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Combined 677CC/1298AC genotypes of methylenetetrahydrofolate reductase (MTHFR ) reduce susceptibility to precursor B lymphoblastic leukemia in a Chinese population

European journal of haematology, 2010-06, Vol.84 (6), p.506-512

2010

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Study of 3D Reconstruction of Laser Welding Pool Surface Based on Shape from Shading

Applied Mechanics and Materials, 2012-10, Vol.201-202, p.344-347

2012

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1656One Case of Pediatric Severepdeudomembranous Enteritis Treated with Fecal Microbiota Transplantation and Literature Review

Open forum infectious diseases, 2014-12, Vol.1 (suppl_1), p.S442-S443

2014

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The Mechanism Study of Serious Gas Explosion Accident at Coal Face

2009 Second International Symposium on Computational Intelligence and Design, 2009, Vol.2, p.239-241

2009

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IEEE_Xplore

The TNF-α 238A polymorphism is associated with susceptibility to persistent bone marrow dysplasia following chronic exposure to benzene

Leukemia research, 2007-11, Vol.31 (11), p.1479-1485

2007

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The TNF-alpha 238A polymorphism is associated with susceptibility to persistent bone marrow dysplasia following chronic exposure to benzene

Leukemia research, 2007-11, Vol.31 (11), p.1479-1485

2007

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Dynamic analysis of rotating flexible disk subjected to double slider loading systems

Theoretical and applied mechanics letters, 2012-01, Vol.2 (6), p.31-36, Article 063004

2012

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Numerical studies of hydrate dissociation and gas production behavior in porous media during depressurization process

Journal of natural gas chemistry, 2012-07, Vol.21 (4), p.381-392

2012

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Origin of the X-chromosome influences the development and treatment outcomes of Turner syndrome

Clinical analysis and genetic diagnosis of three children with Isoleucine metabolic disorders due to variants of HSD17B10 and ACAT1 genes

POLG Mutations Are Probably Rare in the Han Chinese Population

Clinical characteristics and identification of novel CNOT1 variants in three unrelated Chinese families with Vissers-Bodmer Syndrome

Compound heterozygous mutations of NDUFV1 identified in a child with mitochondrial complex I deficiency

Mutation analysis of two pedigrees with suspected oculocutaneous albinism

A rising trend of gastric cardia cancer in Gansu Province of China

Case–control study of risk factors of myelodysplastic syndromes according to World Health Organization classification in a Chinese population

Application of a Multiplex Ligation-Dependent Probe Amplification-Based Next-Generation Sequencing Approach for the Detection of Pathogenesis of Duchenne Muscular Dystrophy and Spinal Muscular Atrophy Caused by Copy Number Aberrations

Adult precursor B lymphoblastic leukemia in Shanghai, China: characterization of phenotype, cytogenetics and outcome for 137 consecutive cases

Prospective study of 174 de novo acute myelogenous leukemias according to the WHO classification: subtypes, cytogenetic features and FLT3 mutations

Compound heterozygous mutations of NDUFV1 identified in a child with mitochondrial complex I deficiency

A multiplex ligation‑dependent probe amplification‑based next‑generation sequencing approach for the detection of copy number variations in the human genome

Genetic mutational profiling analysis of T cell acute lymphoblastic leukemia reveal mutant FBXW7 as a prognostic indicator for inferior survival

A study of two Chinese patients with tetrasomy and pentasomy 15q11q13 including Prader-Willi/Angelman syndrome critical region present with developmental delays and mental impairment

HLA class II alleles may influence susceptibility to adult dermatomyositis and polymyositis in a Han Chinese population

WT1 mutations and single nucleotide polymorphism rs16754 analysis of patients with pediatric acute myeloid leukemia in a Chinese population

Combined 677CC/1298AC genotypes of methylenetetrahydrofolate reductase (MTHFR ) reduce susceptibility to precursor B lymphoblastic leukemia in a Chinese population

Study of 3D Reconstruction of Laser Welding Pool Surface Based on Shape from Shading

1656One Case of Pediatric Severepdeudomembranous Enteritis Treated with Fecal Microbiota Transplantation and Literature Review

The Mechanism Study of Serious Gas Explosion Accident at Coal Face

The TNF-α 238A polymorphism is associated with susceptibility to persistent bone marrow dysplasia following chronic exposure to benzene

The TNF-alpha 238A polymorphism is associated with susceptibility to persistent bone marrow dysplasia following chronic exposure to benzene

Dynamic analysis of rotating flexible disk subjected to double slider loading systems

Numerical studies of hydrate dissociation and gas production behavior in porous media during depressurization process

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