Works matching IS 1178704X AND DT 2014 AND VI 7
Results: 24
Molecular analysis of beta-globin gene mutations among Thai beta-thalassemia children: results from a single center study.
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- Application of Clinical Genetics, 2014, v. 7, p. 253, doi. 10.2147/TACG.S73058
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- Article
Splicing modulation therapy in the treatment of genetic diseases.
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- Application of Clinical Genetics, 2014, v. 7, p. 245, doi. 10.2147/TACG.S71506
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- Article
Ataxia-telangiectasia: future prospects.
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- Application of Clinical Genetics, 2014, v. 7, p. 159, doi. 10.2147/TACG.S35759
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Beckwith-Wiedemann and IMAGe syndromes: two very different diseases caused by mutations on the same gene.
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- Application of Clinical Genetics, 2014, v. 7, p. 169, doi. 10.2147/TACG.S35474
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- Article
New insights into the genetic basis of infertility.
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- Application of Clinical Genetics, 2014, v. 7, p. 235, doi. 10.2147/TACG.S40809
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The genetic basis of Lynch syndrome and its implications for clinical practice and risk management.
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- Application of Clinical Genetics, 2014, v. 7, p. 147, doi. 10.2147/TACG.S51483
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Identification of trisomy 18, trisomy 13, and Down syndrome from maternal plasma.
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- Application of Clinical Genetics, 2014, v. 7, p. 127, doi. 10.2147/TACG.S35602
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- Article
Genetics of hypertrophic cardiomyopathy: advances and pitfalls in molecular diagnosis and therapy.
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- Application of Clinical Genetics, 2014, v. 7, p. 195, doi. 10.2147/TACG.S49126
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Current status of gene therapy for breast cancer: progress and challenges.
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- Application of Clinical Genetics, 2014, v. 7, p. 209, doi. 10.2147/TACG.S54992
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The genetics of Leigh syndrome and its implications for clinical practice and risk management.
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- Application of Clinical Genetics, 2014, v. 7, p. 221, doi. 10.2147/TACG.S46176
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Clinical problems of colorectal cancer and endometrial cancer cases with unknown cause of tumor mismatch repair deficiency (suspected Lynch syndrome).
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- Application of Clinical Genetics, 2014, v. 7, p. 183, doi. 10.2147/TACG.S48625
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- Article
A novel nonsense mutation of the KAL1 gene (p.Trp204*) in Kallmann syndrome.
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- Application of Clinical Genetics, 2014, v. 7, p. 177, doi. 10.2147/TACG.S64280
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Disease-modifying genes and monogenic disorders: experience in cystic fibrosis.
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- Application of Clinical Genetics, 2014, v. 7, p. 133, doi. 10.2147/TACG.S18675
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Optimal management of complications associated with achondroplasia.
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- Application of Clinical Genetics, 2014, v. 7, p. 117, doi. 10.2147/TACG.S51485
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- Article
Angelman syndrome: review of clinical and molecular aspects.
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- Application of Clinical Genetics, 2014, v. 7, p. 93, doi. 10.2147/TACG.S57386
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The genetic basis of ankylosing spondylitis: new insights into disease pathogenesis.
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- Application of Clinical Genetics, 2014, v. 7, p. 105, doi. 10.2147/TACG.S37325
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- Article
Overview of the genetic determinants of primary aldosteronism.
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- Application of Clinical Genetics, 2014, v. 7, p. 67, doi. 10.2147/TACG.S45620
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Influence of oncogenic transcription factors on chromatin conformation and implications in prostate cancer.
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- Application of Clinical Genetics, 2014, v. 7, p. 81, doi. 10.2147/TACG.S35598
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Wiskott-Aldrich syndrome: diagnosis, current management, and emerging treatments.
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- Application of Clinical Genetics, 2014, v. 7, p. 55, doi. 10.2147/TACG.S58444
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- Article
Hypothesis of the neuroendocrine cortisol pathway gene role in the comorbidity of depression, type 2 diabetes, and metabolic syndrome.
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- Application of Clinical Genetics, 2014, v. 7, p. 43, doi. 10.2147/TACG.S39993
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Genetics of bipolar disorder.
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- Application of Clinical Genetics, 2014, v. 7, p. 33, doi. 10.2147/TACG.S39297
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Genetics of bipolar disorder.
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- Application of Clinical Genetics, 2014, v. 7, p. 33, doi. 10.2147/TACG.S39297
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- Article
Pathogenesis of coronary artery disease: focus on genetic risk factors and identification of genetic variants.
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- Application of Clinical Genetics, 2014, v. 7, p. 15, doi. 10.2147/TACG.S35301
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Gene mutations that promote adrenal aldosterone production, sodium retention, and hypertension.
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- Application of Clinical Genetics, 2014, v. 7, p. 1, doi. 10.2147/TACG.S35571
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