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Prenatal diagnosis of chromosomal abnormalities in fetuses with abnormal cardiac ultrasound findings: evaluation of chromosomal microarray‐based analysis

Ultrasound in obstetrics & gynecology, 2013-04, Vol.41 (4), p.375-382

2013

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The effect of TRPM7 suppression on the proliferation, migration and osteogenic differentiation of human dental pulp stem cells

International endodontic journal, 2014-06, Vol.47 (6), p.583-593

2014

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Association analysis between HFM1 variation and primary ovarian insufficiency in Chinese women

Clinical genetics, 2016-05, Vol.89 (5), p.597-602

2016

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Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders

Journal of medical genetics, 2009-04, Vol.46 (4), p.242-248

2009

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A recurrent 1.71 Mb genomic imbalance at 2q13 increases the risk of developmental delay and dysmorphism

Clinical genetics, 2012-03, Vol.81 (3), p.257-264

2012

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Autism-associated Dyrk1a truncation mutants impair neuronal dendritic and spine growth and interfere with postnatal cortical development

Molecular psychiatry, 2018-03, Vol.23 (3), p.747-758

2018

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Genetic analysis of first-trimester miscarriages with a combination of cytogenetic karyotyping, microsatellite genotyping and arrayCGH

Clinical genetics, 2009-02, Vol.75 (2), p.133-140

2009

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ERCC6 founder mutation identified in Finnish patients with COFS syndrome

Clinical genetics, 2010-12, Vol.78 (6), p.541-547

2010

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Clinical features of pulmonary arterial hypertension in young people with an ALK1 mutation and hereditary haemorrhagic telangiectasia

Archives of disease in childhood, 2009-07, Vol.94 (7), p.506-511

2009

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The JAK2/STAT3 and mitochondrial pathways are essential for quercetin nanoliposome-induced C6 glioma cell death

Cell death & disease, 2013-08, Vol.4 (8), p.e746-e746

2013

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The adult galactosemic phenotype

Journal of inherited metabolic disease, 2012-03, Vol.35 (2), p.279-286

2012

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Reduced Penetrance of PRRT2 Mutation in a Chinese Family With Infantile Convulsion and Choreoathetosis Syndrome

Journal of child neurology, 2015-09, Vol.30 (10), p.1263-1269

2015

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High Intensity ras Signaling Induces Premature Senescence by Activating p38 Pathway in Primary Human Fibroblasts

The Journal of biological chemistry, 2004-01, Vol.279 (2), p.1050-1059

2004

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Preparation of sodium fluoride-loaded gelatin microspheres, characterization and cariostatic studies

Journal of microencapsulation, 2004-12, Vol.21 (8), p.889-903

2004

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Effect of traditional Chinese medicine treatment as maintenance therapy on regulating the serum concentration of sCTLA-4 in patients with advanced non-small-cell lung cancer and its relationship with prognosis

Zhōnghuá zhŏngliú zázhì, 2016-10, Vol.38 (10), p.757

2016

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Three-dimensional contrast-enhanced magnetic resonance angiography at 3.0T scanner: significance in the classification of peripheral arterial occlusive disease

International angiology, 2012-04, Vol.31 (2), p.129

2012

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NF1 Microdeletion Syndrome: Refined FISH Characterization of Sporadic and Familial Deletions with Locus-Specific Probes

American journal of human genetics, 2000-01, Vol.66 (1), p.100-109

2000

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Allele-specific replication of 15q11-q13 loci : A diagnostic test for detection of uniparental disomy

American journal of human genetics, 1996-08, Vol.59 (2), p.423-430

1996

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Use of a multiplex PCR/sequencing strategy to detect both connexin 30 (GJB6) 342 kb deletion and connexin 26 (GJB2) mutations in cases of childhood deafness

American journal of medical genetics, 2003-08, Vol.121A (2), p.102-108

2003

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In situ hybridization applied to Waardenburg syndrome

Cytogenetic and genome research, 1993, Vol.63 (1), p.29-32

1993

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Somatic mosaicism for deletion of the entire NF1 gene identified by FISH

Human genetics, 1997-02, Vol.99 (2), p.209-213

1997

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Townes-Brocks syndrome versus expanded spectrum hemifacial microsomia: Review of eight patients and further evidence of a “hot spot” for mutation in the SALL1 gene

Genetics in medicine, 2001-07, Vol.3 (4), p.310-313

2001

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Study on the application value of portable pulse oximeter in adult patients with obstructive sleep apnea

Zhonghua jiehe he huxi zazhi, 2024-06, Vol.47 (6), p.529

2024

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Effect of hypochloric acid on Escherichia coli biofilm and the clinical efficacy of hypochloric acid for wounds with Escherichia coli infection

Zhonghua shao shang yu chuang mian xiu fu za zhi, 2022-03, Vol.38 (3), p.242

2022

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Effects of acute paraquat poisoning on cognitive ability in humans

Zhonghua laodong weisheng zhiyebing zazhi, 2020-11, Vol.38 (11), p.831

2020

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Prenatal diagnosis of chromosomal abnormalities in fetuses with abnormal cardiac ultrasound findings: evaluation of chromosomal microarray‐based analysis

The effect of TRPM7 suppression on the proliferation, migration and osteogenic differentiation of human dental pulp stem cells

Association analysis between HFM1 variation and primary ovarian insufficiency in Chinese women

Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders

A recurrent 1.71 Mb genomic imbalance at 2q13 increases the risk of developmental delay and dysmorphism

Autism-associated Dyrk1a truncation mutants impair neuronal dendritic and spine growth and interfere with postnatal cortical development

Genetic analysis of first-trimester miscarriages with a combination of cytogenetic karyotyping, microsatellite genotyping and arrayCGH

ERCC6 founder mutation identified in Finnish patients with COFS syndrome

Clinical features of pulmonary arterial hypertension in young people with an ALK1 mutation and hereditary haemorrhagic telangiectasia

The JAK2/STAT3 and mitochondrial pathways are essential for quercetin nanoliposome-induced C6 glioma cell death

The adult galactosemic phenotype

Reduced Penetrance of PRRT2 Mutation in a Chinese Family With Infantile Convulsion and Choreoathetosis Syndrome

High Intensity ras Signaling Induces Premature Senescence by Activating p38 Pathway in Primary Human Fibroblasts

Preparation of sodium fluoride-loaded gelatin microspheres, characterization and cariostatic studies

Effect of traditional Chinese medicine treatment as maintenance therapy on regulating the serum concentration of sCTLA-4 in patients with advanced non-small-cell lung cancer and its relationship with prognosis

Three-dimensional contrast-enhanced magnetic resonance angiography at 3.0T scanner: significance in the classification of peripheral arterial occlusive disease

NF1 Microdeletion Syndrome: Refined FISH Characterization of Sporadic and Familial Deletions with Locus-Specific Probes

Allele-specific replication of 15q11-q13 loci : A diagnostic test for detection of uniparental disomy

Use of a multiplex PCR/sequencing strategy to detect both connexin 30 (GJB6) 342 kb deletion and connexin 26 (GJB2) mutations in cases of childhood deafness

In situ hybridization applied to Waardenburg syndrome

Somatic mosaicism for deletion of the entire NF1 gene identified by FISH

Townes-Brocks syndrome versus expanded spectrum hemifacial microsomia: Review of eight patients and further evidence of a “hot spot” for mutation in the SALL1 gene

Study on the application value of portable pulse oximeter in adult patients with obstructive sleep apnea

Effect of hypochloric acid on Escherichia coli biofilm and the clinical efficacy of hypochloric acid for wounds with Escherichia coli infection

Effects of acute paraquat poisoning on cognitive ability in humans

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