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Orphanet Journal of Rare Diseases
|
February 20, 2019
Requirement for etoposide in the treatment of pregnancy related hemophagocytic lymphohistiocytosis: a multicenter retrospective study
Yue Song, Zhao Wang, Zengping Hao, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao
|
January 4, 2011
Identification of a novel mutation in POU3F4 for prenatal diagnosis in a Chinese family with X-linked nonsyndromic hearing loss
Jianzhong Li, Jing Cheng, Yanping Lu, et al.
Scientific Reports
|
February 18, 2018
The gastrointestinal tract microbiota of northern white-cheeked gibbons (Nomascus leucogenys) varies with age and captive condition
Ting Jia, Sufen Zhao, Katrina Knott, et al.
Plos One
|
August 13, 2013
Identification of a Novel TECTA mutation in a Chinese DFNA8/12 family with prelingual progressive sensorineural hearing impairment
Zhengyue Li, Yilian Guo, Yu Lu, et al.
International Journal of Food Microbiology
|
January 27, 2026
Strain-specific impacts of Pichia kudriavzevii on metabolite profiles and microbial community dynamics in Chinese Baijiu fermentation: Integrated metabolomics and metagenomics analysis
Boqin Zhang, Mengbo Wang, Jia Zheng, et al.
International Journal of Clinical and Experimental Pathology
|
July 21, 2015
A missense mutation in TMEM67 causes Meckel-Gruber syndrome type 3 (MKS3): a family from China
Manli Zhang, Jing Cheng, Aijun Liu, et al.
Prenatal Diagnosis
|
July 27, 2018
Noninvasive prenatal test for FGFR3-related skeletal dysplasia based on next-generation sequencing and plasma cell-free DNA: Test performance analysis and feasibility exploration
Yuan Ren, Jia Zhao, Ruibing Li, et al.
Journal of Physiological Investigation
|
September 5, 2025
Niujiaodihuang Detoxify Decoction Inhibits D-GalN/LPS-induced Hepatocyte Ferroptosis by Maintaining Mitochondrial Homeostasis Via OMA1-OPA1 Pathway
Yanping Lu, Henghui Sun, Qinyan Zhu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 26, 2017
A quantitative cSMART assay for noninvasive prenatal screening of autosomal recessive nonsyndromic hearing loss caused by GJB2 and SLC26A4 mutations
Mingyu Han, Zhifeng Li, Wenlu Wang, et al.
Prenatal Diagnosis
|
June 6, 2021
Combined exome sequencing and deep phenotyping in highly selected fetuses with skeletal dysplasia during the first and second trimesters improves diagnostic yield
Xinyue Zhang, Yuan Ren, Rui Song, et al.
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Search research articles
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Showing results (61-70 of 82) with videos related to
Sort By:
Page
of 9
Orphanet Journal of Rare Diseases
|
February 20, 2019
Requirement for etoposide in the treatment of pregnancy related hemophagocytic lymphohistiocytosis: a multicenter retrospective study
Yue Song, Zhao Wang, Zengping Hao, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao
|
January 4, 2011
Identification of a novel mutation in POU3F4 for prenatal diagnosis in a Chinese family with X-linked nonsyndromic hearing loss
Jianzhong Li, Jing Cheng, Yanping Lu, et al.
Scientific Reports
|
February 18, 2018
The gastrointestinal tract microbiota of northern white-cheeked gibbons (Nomascus leucogenys) varies with age and captive condition
Ting Jia, Sufen Zhao, Katrina Knott, et al.
Plos One
|
August 13, 2013
Identification of a Novel TECTA mutation in a Chinese DFNA8/12 family with prelingual progressive sensorineural hearing impairment
Zhengyue Li, Yilian Guo, Yu Lu, et al.
International Journal of Food Microbiology
|
January 27, 2026
Strain-specific impacts of Pichia kudriavzevii on metabolite profiles and microbial community dynamics in Chinese Baijiu fermentation: Integrated metabolomics and metagenomics analysis
Boqin Zhang, Mengbo Wang, Jia Zheng, et al.
International Journal of Clinical and Experimental Pathology
|
July 21, 2015
A missense mutation in TMEM67 causes Meckel-Gruber syndrome type 3 (MKS3): a family from China
Manli Zhang, Jing Cheng, Aijun Liu, et al.
Prenatal Diagnosis
|
July 27, 2018
Noninvasive prenatal test for FGFR3-related skeletal dysplasia based on next-generation sequencing and plasma cell-free DNA: Test performance analysis and feasibility exploration
Yuan Ren, Jia Zhao, Ruibing Li, et al.
Journal of Physiological Investigation
|
September 5, 2025
Niujiaodihuang Detoxify Decoction Inhibits D-GalN/LPS-induced Hepatocyte Ferroptosis by Maintaining Mitochondrial Homeostasis Via OMA1-OPA1 Pathway
Yanping Lu, Henghui Sun, Qinyan Zhu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 26, 2017
A quantitative cSMART assay for noninvasive prenatal screening of autosomal recessive nonsyndromic hearing loss caused by GJB2 and SLC26A4 mutations
Mingyu Han, Zhifeng Li, Wenlu Wang, et al.
Prenatal Diagnosis
|
June 6, 2021
Combined exome sequencing and deep phenotyping in highly selected fetuses with skeletal dysplasia during the first and second trimesters improves diagnostic yield
Xinyue Zhang, Yuan Ren, Rui Song, et al.
Page
of 9