Found: 138
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Chromosome microarray analysis in the investigation of children with congenital heart disease.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Microcapsule Modification Strategy Empowering Separator Multifunctionality to Enhance Safety of Lithium‐Metal Batteries.
- Published in:
- Small, 2024, v. 20, n. 43, p. 1, doi. 10.1002/smll.202404470
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- Publication type:
- Article
Advanced Polymer Materials for Protecting Lithium Metal Anodes of Liquid‐State and Solid‐State Lithium Batteries.
- Published in:
- Advanced Functional Materials, 2024, v. 34, n. 42, p. 1, doi. 10.1002/adfm.202404427
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- Publication type:
- Article
Damage identification based on convolutional neural network and recurrence graph for beam bridge.
- Published in:
- Structural Health Monitoring, 2021, v. 20, n. 4, p. 1392, doi. 10.1177/1475921720916928
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- Publication type:
- Article
Non‐Flammable Electrolyte with Lithium Nitrate as the Only Lithium Salt for Boosting Ultra‐Stable Cycling and Fire‐Safety Lithium Metal Batteries.
- Published in:
- Advanced Functional Materials, 2023, v. 33, n. 17, p. 1, doi. 10.1002/adfm.202212605
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- Publication type:
- Article
Phosphorus‐Fixed Stable Interfacial Nonflammable Gel Polymer Electrolyte for Safe Flexible Lithium‐Ion Batteries.
- Published in:
- Advanced Functional Materials, 2022, v. 32, n. 35, p. 1, doi. 10.1002/adfm.202203006
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- Publication type:
- Article
PDIA2 variant associated with vitiligo.
- Published in:
- Skin Health & Disease, 2023, v. 3, n. 5, p. 1, doi. 10.1002/ski2.278
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- Publication type:
- Article
Ultrathin and Mechanically Robust Mussel Byssus‐Inspired MXene@Aramid Nanofibers Materials with Superior Endurance in Harsh Environments for Tunable EMI Shielding Performance.
- Published in:
- Advanced Materials Interfaces, 2022, v. 9, n. 5, p. 1, doi. 10.1002/admi.202101359
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- Publication type:
- Article
Functional analysis of a novel splice site variant in the ASAH1 gene.
- Published in:
- Molecular Genetics & Genomic Medicine, 2024, v. 12, n. 1, p. 1, doi. 10.1002/mgg3.2317
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- Publication type:
- Article
Prenatal diagnosis and perinatal outcomes of twin pregnancies disharmonious for one fetus with nuchal translucency above the 95th percentile.
- Published in:
- Molecular Cytogenetics (17558166), 2023, v. 16, n. 1, p. 1, doi. 10.1186/s13039-023-00659-9
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- Publication type:
- Article
Prenatal diagnosis and early childhood outcome of fetuses with extremely large nuchal translucency.
- Published in:
- Molecular Cytogenetics (17558166), 2023, v. 16, n. 1, p. 1, doi. 10.1186/s13039-023-00650-4
- By:
- Publication type:
- Article
Prenatal diagnosis of Williams-Beuren syndrome by ultrasound and chromosomal microarray analysis.
- Published in:
- 2022
- By:
- Publication type:
- Case Study
Fetal karyotyping and late sonographic abnormality detection in China
- Published in:
- 2008
- By:
- Publication type:
- journal article
Efficacy and safety of cordocentesis for prenatal diagnosis
- Published in:
- 2006
- By:
- Publication type:
- journal article
Prenatal diagnosis and molecular analysis of type 1 thanatophoric dysplasia
- Published in:
- 2005
- By:
- Publication type:
- journal article
Molecular epidemiology and hematologic characterization of δβ-thalassemia and hereditary persistence of fetal hemoglobin in 125,661 families of greater Guangzhou area, the metropolis of southern China.
- Published in:
- BMC Medical Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s12881-020-0981-x
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- Publication type:
- Article
Innentitelbild: A Supported Catalyst that Enables the Synthesis of Colorless CO<sub>2</sub>‐Polyols with Ultra‐Low Molecular Weight (Angew. Chem. 35/2023).
- Published in:
- Angewandte Chemie, 2023, v. 135, n. 35, p. 1, doi. 10.1002/ange.202308125
- By:
- Publication type:
- Article
A Supported Catalyst that Enables the Synthesis of Colorless CO<sub>2</sub>‐Polyols with Ultra‐Low Molecular Weight.
- Published in:
- Angewandte Chemie, 2023, v. 135, n. 35, p. 1, doi. 10.1002/ange.202305186
- By:
- Publication type:
- Article
Cobalt‐Mediated Switchable Catalysis for the One‐Pot Synthesis of Cyclic Polymers.
- Published in:
- Angewandte Chemie, 2021, v. 133, n. 31, p. 17111, doi. 10.1002/ange.202106285
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- Publication type:
- Article
All‐trans‐retinoid acid induces the differentiation of P19 cells into neurons involved in the PI3K/Akt/GSK3β signaling pathway.
- Published in:
- Journal of Cellular Biochemistry, 2020, v. 121, n. 11, p. 4386, doi. 10.1002/jcb.29659
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- Publication type:
- Article
Prenatal diagnosis in the fetal hyperechogenic kidneys: assessment using chromosomal microarray analysis and exome sequencing.
- Published in:
- Human Genetics, 2023, v. 142, n. 6, p. 835, doi. 10.1007/s00439-023-02545-1
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- Publication type:
- Article
Whole exome sequencing improves genetic diagnosis of fetal clubfoot.
- Published in:
- Human Genetics, 2023, v. 142, n. 3, p. 407, doi. 10.1007/s00439-022-02516-y
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- Publication type:
- Article
Compound heterozygous mutation of the ASXL3 gene causes autosomal recessive congenital heart disease.
- Published in:
- Human Genetics, 2021, v. 140, n. 2, p. 333, doi. 10.1007/s00439-020-02200-z
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- Publication type:
- Article
Co-inheritance of α-thalassaemia and β-thalassaemia in a prenatal screening population in mainland China.
- Published in:
- Journal of Medical Screening, 2014, v. 21, n. 4, p. 167, doi. 10.1177/0969141314548203
- By:
- Publication type:
- Article
Co-inheritance of α-thalassaemia and β-thalassaemia in a prenatal screening population in mainland China.
- Published in:
- 2014
- By:
- Publication type:
- Journal Article
Phase‐Controlled Synthesis and Quasi‐Static Dielectric Resonances in Silver Iron Sulfide (AgFeS<sub>2</sub>) Nanocrystals.
- Published in:
- Small, 2022, v. 18, n. 9, p. 1, doi. 10.1002/smll.202104975
- By:
- Publication type:
- Article
Prenatal exome sequencing in fetuses with congenital heart defects.
- Published in:
- Clinical Genetics, 2020, v. 98, n. 3, p. 215, doi. 10.1111/cge.13774
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- Publication type:
- Article
Three Hemoglobin Variants Caused by a Single α-Chain Gene Mutation in a Chinese Family.
- Published in:
- Acta Haematologica, 2010, v. 123, n. 2, p. 88, doi. 10.1159/000267213
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- Publication type:
- Article
Association of prenatal Cleft Lip and Palate ultrasound abnormalities with copy number variants at a single Chinese tertiary center.
- Published in:
- Italian Journal of Pediatrics, 2024, v. 50, n. 1, p. 1, doi. 10.1186/s13052-024-01720-y
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- Publication type:
- Article
The performance of a new type accelerator uRT‐linac 506c evaluated by a quality assurance automation system.
- Published in:
- Journal of Applied Clinical Medical Physics, 2024, v. 25, n. 1, p. 1, doi. 10.1002/acm2.14226
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- Publication type:
- Article
Simulation Research on Safe Flow Rate of Bidirectional Crowds Using Bayesian-Nash Equilibrium.
- Published in:
- Complexity, 2019, p. 1, doi. 10.1155/2019/7942483
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- Publication type:
- Article
Microarray analysis in fetuses with duodenal obstruction: It is not just trisomy 21.
- Published in:
- Prenatal Diagnosis, 2021, v. 41, n. 3, p. 316, doi. 10.1002/pd.5834
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- Publication type:
- Article
Whole‐exome sequencing in the evaluation of fetal congenital anomalies of the kidney and urinary tract detected by ultrasonography.
- Published in:
- Prenatal Diagnosis, 2020, v. 40, n. 10, p. 1290, doi. 10.1002/pd.5737
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- Publication type:
- Article
Genetic tests aid in counseling of fetuses with cerebellar vermis defects.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Nonimmune hydrops fetalis: Genetic analysis and clinical outcome.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Rapid prenatal diagnosis of skeletal dysplasia using medical trio exome sequencing: Benefit for prenatal counseling and pregnancy management.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Corrigendum for Li D, Lin Y, Huang Y, et al (2018) https://doi.org/10.1002/pd.5329.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Early prenatal diagnosis of lysosomal storage disorders by enzymatic and molecular analysis.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Pregnancy outcome of autosomal aneuploidies other than common trisomies detected by noninvasive prenatal testing in routine clinical practice.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Outcome of isolated enlarged cisterna magna identified in utero: experience at a single medical center in mainland China.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Prenatal diagnosis of congenital heart defect by genome-wide high-resolution SNP array.
- Published in:
- Prenatal Diagnosis, 2014, v. 34, n. 9, p. 858, doi. 10.1002/pd.4383
- By:
- Publication type:
- Article
Prenatal control of nondeletional [alpha]-thalassemia: first experience in mainland China.
- Published in:
- 2013
- By:
- Publication type:
- Journal Article
Prenatal control of nondeletional α-thalassemia: first experience in mainland China.
- Published in:
- Prenatal Diagnosis, 2013, v. 33, n. 9, p. 869, doi. 10.1002/pd.4149
- By:
- Publication type:
- Article
Discordant results between fetal karyotyping and non-invasive prenatal testing by maternal plasma sequencing in a case of uniparental disomy 21 due to trisomic rescue.
- Published in:
- Prenatal Diagnosis, 2013, v. 33, n. 6, p. 598, doi. 10.1002/pd.4069
- By:
- Publication type:
- Article
Acceptability of supplementary QF-PCR among women undergoing prenatal diagnosis in mainland China.
- Published in:
- Prenatal Diagnosis, 2012, v. 32, n. 8, p. 813, doi. 10.1002/pd.3897
- By:
- Publication type:
- Article
Prenatal diagnosis of hemoglobin Bart's disease caused by co-inheritance of two different alpha 0-thalassemia defects in China.
- Published in:
- 2009
- By:
- Publication type:
- case study
Prenatal diagnosis of hemoglobin Bart's disease caused by co-inheritance of two different α<sup>0</sup>-thalassemia defects in China.
- Published in:
- Prenatal Diagnosis, 2009, v. 29, n. 6, p. 632, doi. 10.1002/pd.2259
- By:
- Publication type:
- Article
Fetal anemia and hydrops associated with homozygosity for hemoglobin Quong Sze.
- Published in:
- Prenatal Diagnosis, 2008, v. 28, n. 9, p. 862, doi. 10.1002/pd.2058
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- Publication type:
- Article
Pregnancy outcome following prenatal diagnosis of sex chromosome abnormalities in Mainland China.
- Published in:
- Prenatal Diagnosis, 2008, v. 28, n. 5, p. 443, doi. 10.1002/pd.1982
- By:
- Publication type:
- Article
A case of transfusion-dependent nondeletional Hb H disease undiagnosed during prenatal screening for thalassemia.
- Published in:
- Prenatal Diagnosis, 2008, v. 28, n. 2, p. 165, doi. 10.1002/pd.1947
- By:
- Publication type:
- Article