Works matching IS 1178704X AND DT 2016 AND VI 9
Results: 23
The association between vitamin D receptor gene polymorphisms (TaqI and FokI), Type 2 diabetes, and micro-/macrovascular complications in postmenopausal women.
- Published in:
- Application of Clinical Genetics, 2016, v. 9, p. 131, doi. 10.2147/TACG.S101410
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- Publication type:
- Article
Examining genotypic variation in autism spectrum disorder and its relationship to parental age and phenotype.
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- Application of Clinical Genetics, 2016, v. 9, p. 121, doi. 10.2147/TACG.S112712
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- Article
Authors' response.
- Published in:
- 2016
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- Publication type:
- Letter to the Editor
Advances in the management of erythropoietic protoporphyria - role of afamelanotide.
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- Application of Clinical Genetics, 2016, v. 9, p. 179, doi. 10.2147/tacg.s122030
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- Article
Analysis of binary responses with outcome-specific misclassification probability in genome-wide association studies.
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- Application of Clinical Genetics, 2016, v. 9, p. 169, doi. 10.2147/TACG.S122250
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- Article
Novel treatment options for lysosomal acid lipase deficiency: critical appraisal of sebelipase alfa.
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- Application of Clinical Genetics, 2016, v. 9, p. 157, doi. 10.2147/TACG.S86760
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- Article
The genetics of uveal melanoma: current insights.
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- Application of Clinical Genetics, 2016, v. 9, p. 147
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- Article
Animal models of GM2 gangliosidosis: utility and limitations.
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- Application of Clinical Genetics, 2016, v. 9, p. 111, doi. 10.2147/TACG.S85354
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- Article
ROCK2 and MYLK variants and high-altitude pulmonary edema.
- Published in:
- 2016
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- Publication type:
- Letter to the Editor
Identification of a novel pathogenic OTOF variant causative of nonsyndromic hearing loss with high frequency in the Ashkenazi Jewish population.
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- Application of Clinical Genetics, 2016, v. 9, p. 141, doi. 10.2147/TACG.S113828
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- Article
Mevalonate kinase deficiency: current perspectives.
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- Application of Clinical Genetics, 2016, v. 9, p. 101, doi. 10.2147/TACG.S93933
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- Article
Utilization of genetic testing among children with developmental disabilities in the United States.
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- Application of Clinical Genetics, 2016, v. 9, p. 93, doi. 10.2147/TACG.S103975
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- Article
Alagille syndrome: clinical perspectives.
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- Application of Clinical Genetics, 2016, v. 9, p. 75, doi. 10.2147/TACG.S86420
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- Article
Genetic basis of Cowden syndrome and its implications for clinical practice and risk management.
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- Application of Clinical Genetics, 2016, v. 9, p. 83, doi. 10.2147/TACG.S41947
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- Publication type:
- Article
Role of elosulfase alfa in mucopolysaccharidosis IVA.
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- Application of Clinical Genetics, 2016, v. 9, p. 67, doi. 10.2147/TACG.S69080
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- Publication type:
- Article
Genetics of Lafora progressive myoclonic epilepsy: current perspectives.
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- Application of Clinical Genetics, 2016, v. 9, p. 49, doi. 10.2147/TACG.S57890
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- Publication type:
- Article
Marfan syndrome: current perspectives.
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- Application of Clinical Genetics, 2016, v. 9, p. 55, doi. 10.2147/TACG.S96233
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- Publication type:
- Article
Natural killer cells and single nucleotide polymorphisms of specific ion channels and receptor genes in myalgic encephalomyelitis/ chronic fatigue syndrome.
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- Application of Clinical Genetics, 2016, v. 9, p. 39, doi. 10.2147/TACG.S99405
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- Article
Analysis of the CFTR gene in Venezuelan cystic fibrosis patients, identification of six novel cystic fibrosis-causing genetic variants.
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- Application of Clinical Genetics, 2016, v. 9, p. 33, doi. 10.2147/TACG.S78241
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- Article
Non-invasive prenatal testing for fetal chromosome abnormalities: review of clinical and ethical issues.
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- Application of Clinical Genetics, 2016, v. 9, p. 15, doi. 10.2147/TACG.S85361
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- Publication type:
- Article
Emery-Dreifuss muscular dystrophy: a test case for precision medicine.
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- Application of Clinical Genetics, 2016, v. 9, p. 27, doi. 10.2147/TACG.S75028
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- Publication type:
- Article
Candidate genes of idiopathic pulmonary fibrosis: current evidence and research.
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- Application of Clinical Genetics, 2016, v. 9, p. 5, doi. 10.2147/TACG.S61999
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- Publication type:
- Article
Case report of individual with cutaneous immunodeficiency and novel 1p36 duplication.
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- Application of Clinical Genetics, 2016, v. 9, p. 1, doi. 10.2147/TACG.S90713
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- Publication type:
- Article