Turner's syndrome female with a small ring (X) and 15q13.3 microdeletion syndrome identified by High-Density Array

Fernandez R.; Mallo M.; Sole F.; Cortes-Cortes J.; Lopez-Siguero J. P.; Pasaro E.

首页> 外文期刊>Chromosome research: An international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology >Turner's syndrome female with a small ring (X) and 15q13.3 microdeletion syndrome identified by High-Density Array

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Turner's syndrome female with a small ring (X) and 15q13.3 microdeletion syndrome identified by High-Density Array

机译：特纳综合征女性具有小环（X）和15Q13.3微缺综合度综合征，由高密度阵列鉴定

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《Chromosome research: An international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology 》 |2015年第2期| 共1页
作者
Fernandez R.; Mallo M.; Sole F.; Cortes-Cortes J.; Lopez-Siguero J. P.; Pasaro E.;
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作者单位

Univ A Coruna Dept Psicobiol La Coruna Spain;

Hosp Mar Serv Patol Lab Citol Hematol Barcelona Spain;

Hosp Mar Serv Patol Lab Citol Hematol Barcelona Spain;

Univ A Coruna Dept Psicobiol La Coruna Spain;

Hosp Materno Infantil Carlos Haya Serv Endocrinol Pediat Malaga Spain;

Univ A Coruna Dept Psicobiol La Coruna Spain;

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正文语种 eng
中图分类医学遗传学 ;
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1. Turner's syndrome female with a small ring (X) and 15q13.3 microdeletion syndrome identified by High-Density Array [J] . Fernandez R., Mallo M., Sole F., Chromosome research: An international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology . 2015 ,第2期

机译：通过高密度阵列鉴定的特纳氏综合症女性，有小环（X）和15q13.3微缺失综合症
2. High-resolution single nucleotide polymorphism arrays identified an atypical microdeletion of the Williams-Beuren syndrome interval in a patient presenting with a different phenotype [J] . Hu Shijun, Yang Yifeng, Liu Lin, Molecular medicine reports . 2017 ,第5aPta1期

机译：高分辨率单核苷酸多态性阵列鉴定了用不同表型呈现出患者患者威廉姆斯 - 贝仑综合征间隔的非典型微缺失
3. Array-CGH in unclear syndromic nephropathies identifies a microdeletion in Xq22.3-q23 [J] . Alexander Hoischen, Christina Landwehr, Sarah Kabisch, Pediatric Nephrology . 2009 ,第9期

机译：症状不明的肾病肾病中的Array-CGH识别Xq22.3-q23中的微缺失
4. An intelligent web-based system for the detection and visualization of biomarkers in Microdeletion and Microduplication Syndromes [C] . Konstantinos Stefanou, Christos Bellos, Georgios Stergios, IEEE International Conference on Bioinformatics and Bioengineering . 2020

机译：基于智能网络的系统，用于检测和可视化微缺失和微杂皮综合征中的生物标志物
5. The New Face of Genetics: Education of the Medical Community to Improve Patient Satisfaction. A Comparison of 22q11.2 Deletion Syndrome and Turner Syndrome. [D] . Moser, Cory R. 2013

机译：遗传学的新面貌：医学界对提高患者满意度的教育。 22q11.2删除综合征和特纳综合征的比较。
6. The Use of High-Density SNP Array to Map Homozygosity in Consanguineous Families to Efficiently Identify Candidate Genes: Application to Woodhouse-Sakati Syndrome [O] . Molly B. Sheridan, Elizabeth Wohler, Denise A. S. Batista, 2015

机译：使用高密度SNP阵列来映射血缘家庭的纯合子以有效地识别候选基因：在Woodhouse-Sakati综合征中的应用
7. The Use of High-Density SNP Array to Map Homozygosity in Consanguineous Families to Efficiently Identify Candidate Genes: Application to Woodhouse-Sakati Syndrome [O] . Molly B. Sheridan, Elizabeth Wohler, Denise A. S. Batista, 2015

机译：使用高密度SNP阵列在近亲家庭中映射纯合性，以有效识别候选基因：在Woodhouse-Sakati综合征中的应用

Turner's syndrome female with a small ring (X) and 15q13.3 microdeletion syndrome identified by High-Density Array

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