Works matching IS 1178704X AND DT 2012 AND VI 5

Results: 12

Association of deletion allele of insertion/deletion polymorphism in α2B adrenoceptor gene and hypertension with or without type 2 diabetes mellitus.

Published in:

Application of Clinical Genetics, 2012, v. 5, p. 111, doi. 10.2147/TACG.S33814

By:

Tayel, Safaa I.;
Khader, Heba F.;
El-Helbawy, Nesreen G.;
Ibrahim, Waleed A.

Publication type:

Article

Genetics of hearing loss: focus on DFNA2.

Published in:

Application of Clinical Genetics, 2012, v. 5, p. 97, doi. 10.2147/TACG.S35525

By:

Dominguez, Laura M.;
Dodson, Kelley M.

Publication type:

Article

Gene therapy for the treatment of cystic fibrosis.

Published in:

Application of Clinical Genetics, 2012, v. 5, p. 29, doi. 10.2147/TACG.S8873

By:

Burney, Tabinda J.;
Davies, Jane C.

Publication type:

Article

Clinical and molecular characterization of a patient with a combination of a deletion and a duplication of 22q13 using array CGH.

Published in:

Application of Clinical Genetics, 2012, v. 5, p. 93, doi. 10.2147/TACG.S35799

By:

Ochando, Isabel;
Urbano, Antonio;
Rubio, Juana;
Rueda, Joaquín

Publication type:

Article

The genetics of neuroendocrine prostate cancers: a review of current and emerging candidates.

Published in:

Application of Clinical Genetics, 2012, v. 5, p. 105, doi. 10.2147/TACG.S28881

By:

Hammad Ather, M.;
Siddiqui, Tahmeena

Publication type:

Article

Association analysis of genetic variations of eNOS and α<sub>2</sub>β<sub>1</sub> integrin genes with type 2 diabetic retinopathy.

Published in:

Application of Clinical Genetics, 2012, v. 5, p. 55, doi. 10.2147/TACG.S31979

By:

Azmy, Rania;
Dawood, Ashraf;
Kilany, Ayman;
El-Ghobashy, Yasser;
Ellakwa, Amin Faisal;
El-Daly, May

Publication type:

Article

Familial amyloidotic polyneuropathy: current and emerging treatment options for transthyretin-mediated amyloidosis.

Published in:

Application of Clinical Genetics, 2012, v. 5, p. 37, doi. 10.2147/TACG.S19903

By:

Hund, Ernst

Publication type:

Article

The genetic basis of severe combined immunodeficiency and its variants.

Published in:

Application of Clinical Genetics, 2012, v. 5, p. 67, doi. 10.2147/TACG.S18693

By:

Tasher, Diana;
Dalal, Ilan

Publication type:

Article

Skeletal muscle SIRT1 and the genetics of metabolic health: therapeutic activation by pharmaceuticals and exercise.

Published in:

Application of Clinical Genetics, 2012, v. 5, p. 81, doi. 10.2147/TACG.S31276

By:

Williams, Cameron B.;
Gurd, Brendon J.

Publication type:

Article

Clinical applications of schizophrenia genetics: genetic diagnosis, risk, and counseling in the molecular era.

Published in:

Application of Clinical Genetics, 2012, v. 5, p. 1, doi. 10.2147/TACG.S21953

By:

Costain, Gregory;
Bassett, Anne S.

Publication type:

Article

Congenital protein hypoglycosylation diseases.

Published in:

Application of Clinical Genetics, 2012, v. 5, p. 43, doi. 10.2147/TACG.S18673

By:

Sparks, Susan E.

Publication type:

Article

Chronic lymphocytic leukemia-associated chromosomal abnormalities and miRNA deregulation.

Published in:

Application of Clinical Genetics, 2012, v. 5, p. 21, doi. 10.2147/TACG.S18669

By:

Kiefer, Yvonne;
Schulte, Christoph;
Tiemann, Markus;
Bullerdiek, Joern

Publication type:

Article