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Academic Journal

[Analysis of results of concurrent hearing and deafness genetic screening and follow up of 33 911 newborns].

  • Authors : Lei J; Department of Clinical Laboratory, Shenzhen Nanshan Maternity and Child Health Care Hospital, Shenzhen, Guangdong 518067, China. .; Han L

Subjects: Deafness*/Deafness*/Deafness*/epidemiology ; Deafness*/Deafness*/Deafness*/genetics ; Genetic Testing*/Genetic Testing*/Genetic Testing*/statistics & numerical data

  • Source: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics [Zhonghua Yi Xue Yi Chuan Xue Za Zhi] 2021 Jan Publisher: Sichuan University Country of Publication: China NLM ID: 9425197 Publication Model: Print Cited Medium: Print ISSN: 1003-9406 (Print)

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Academic Journal

[Advances in genetic screening for neonatal diseases].

  • Authors : Zhang WR; Department of Genetic and Metabolic Diseases, the Children's Hospital of Zhejiang University School of Medicine, Hangzhou 310052, China.; Zhao ZY

Subjects: Genetic Testing* ; Infant, Newborn, Diseases* ; Neonatal Screening*

  • Source: Zhonghua er ke za zhi = Chinese journal of pediatrics [Zhonghua Er Ke Za Zhi] 2020 Dec 02; Vol. 58 (12), pp. 1033-1037.Publisher: Chinese Medical Association Country of Publication: China NLM ID: 0417427 Publication Model: Print Cited Medium:

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Academic Journal

[Genetic Screening of Thalassemia among the Couples of Childbearing Age in Ding'an County of Hainan Province and Its Analysis].

  • Authors : Tu ZH; Reproductive Medical Center, Maternal and Child Health Care Hospital of Hainan Province, Haikou 570206,Hainan Province, China.; Wang J

Subjects: Genetic Testing* ; alpha-Thalassemia* ; beta-Thalassemia*

  • Source: Zhongguo shi yan xue ye xue za zhi [Zhongguo Shi Yan Xue Ye Xue Za Zhi] 2019 Oct; Vol. 27 (5), pp. 1592-1595.Publisher: Zhongguo shi yan xue za zhi she Country of Publication: China NLM ID: 101084424 Publication Model: Print Cited Medium: Print ISSN:

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Academic Journal

[Genetic screening in early diagnosis of neonatal WAS gene-related disorders].

  • Authors : Liu X; Department of Neonatology, Children's Hospital of Fudan University, Shanghai 201102, China.; Yang L

Subjects: Genetic Diseases, X-Linked*; Genetic Testing/Genetic Testing/Genetic Testing/*methods ; Thrombocytopenia/Thrombocytopenia/Thrombocytopenia/*diagnosis

  • Source: Zhonghua er ke za zhi = Chinese journal of pediatrics [Zhonghua Er Ke Za Zhi] 2019 Jun 02; Vol. 57 (6), pp. 429-433.Publisher: Chinese Medical Association Country of Publication: China NLM ID: 0417427 Publication Model: Print Cited Medium:

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Academic Journal

[Genetic screening and prenatal diagnosis in 18 high-risk families with 21-hydroxylase deficiency].

  • Authors : Xia Y; Prenatal Diagnosis Center, the First Affiliated Hospital, Zhengzhou University, Zhengzhou, Henan 450052, China. .; Mei S

Subjects: Genetic Testing*; Adrenal Hyperplasia, Congenital/Adrenal Hyperplasia, Congenital/Adrenal Hyperplasia, Congenital/*diagnosis; Adrenal Hyperplasia, Congenital/Adrenal Hyperplasia, Congenital/Adrenal Hyperplasia, Congenital/genetics Congenital adrenal hyperplasia due to 21 hydroxylase deficiency

  • Source: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics [Zhonghua Yi Xue Yi Chuan Xue Za Zhi] 2019 Feb Publisher: Sichuan University Country of Publication: China NLM ID: 9425197 Publication Model: Print Cited Medium: Print ISSN: 1003-9406 (Print)

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Academic Journal

[Functional genetic screening using CRISPR-Cas9 system].

  • Authors : Li H; National Institute of Diagnostics and Vaccine Development in Infectious Dciseases, State Key Laboratory of Molecular Vaccinology and Molecular Diagnostics, School of Life Sciences, Xiamen University, Xiamen 361102, Fujian, China.; Huang C

Subjects: CRISPR-Cas Systems* ; Gene Editing* ; Genetic Testing*

  • Source: Sheng wu gong cheng xue bao = Chinese journal of biotechnology [Sheng Wu Gong Cheng Xue Bao] 2018 Apr 25; Vol. 34 (4), pp. 461-472.Publisher: Ke xue chu ban she Country of Publication: China NLM ID: 9426463 Publication Model: Print Cited Medium: Internet ISSN: 1872-2075

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Academic Journal

[Pre-implantation genetic screening of discarded embryos through whole genome amplification and next-generation sequencing].

  • Authors : Zhu Y; Department of Laboratory Medicine, Maternal and Child Health Care Hospital of Huzhou, Huzhou, Zhejiang 313000, China. .; Liu C

Subjects: Fetal Diseases/Fetal Diseases/Fetal Diseases/*genetics ; High-Throughput Nucleotide Sequencing/High-Throughput Nucleotide Sequencing/High-Throughput Nucleotide Sequencing/*methods ; Preimplantation Diagnosis/Preimplantation Diagnosis/Preimplantation Diagnosis/*methods

  • Source: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics [Zhonghua Yi Xue Yi Chuan Xue Za Zhi] 2018 Jun Publisher: Sichuan University Country of Publication: China NLM ID: 9425197 Publication Model: Print Cited Medium: Print ISSN: 1003-9406 (Print)

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Academic Journal

[The significance of pedigree genetic screening and rapid immunological parameters in the diagnosis of primary hemophagocytic lymphohistiocytosis].

  • Authors : Zhang J; Department of Hematology, Beijing Friendship Hospital, Capital Medical University, Beijing 100050, China.; Wang YN

Subjects: Genetic Testing*; Lymphohistiocytosis, Hemophagocytic/Lymphohistiocytosis, Hemophagocytic/Lymphohistiocytosis, Hemophagocytic/*diagnosis ; Lymphohistiocytosis, Hemophagocytic/Lymphohistiocytosis, Hemophagocytic/Lymphohistiocytosis, Hemophagocytic/*genetics

  • Source: Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi [Zhonghua Xue Ye Xue Za Zhi] 2016 Jul; Vol. 37 (7), pp. 565-70.Publisher: Chinese Medical Association Country of Publication: China NLM ID: 8212398 Publication Model: Print Cited Medium:

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Academic Journal

[Children's hearing behavior observations and high risk individual genetic screening for late-onset hearing loss early detection and intervention exploring a basic-level hospitals model].

Subjects: Behavior Observation Techniques* ; Genetic Testing*; Deafness/Deafness/Deafness/*diagnosis

  • Source: Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery [Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi] 2015 Sep; Vol. 29 (18),Publisher: Lin chuang er bi yan hou tou jing wai ke za zhi bain ji bu Country of Publication: China NLM ID: 101303164 Publication Model: Print Cited Medium:

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Academic Journal

[Study of newborn hearing and genetic screening in Jinan].

  • Authors : Xiang L; Department of Newborn Hearing Screening, Jinan Maternity and Child Care Hospital, Jinnan 250001, China.; Lin Q

Subjects: Genetic Testing* ; Hearing Tests* ; Neonatal Screening*

  • Source: Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery [Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi]Publisher: Zhonghua yi xue hui za zhi she Country of Publication: China NLM ID: 101247574 Publication Model: Print Cited Medium: Print ISSN:

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  • 1-10 of  656 results for ""Genetic screening""