Works matching IS 00034800 AND DT 2015 AND VI 79 AND IP 1

Results: 9

Identification and Molecular Characterization of HNF1B Gene Mutations in Indian Diabetic Patients with Renal Abnormalities.

Published in:

Annals of Human Genetics, 2015, v. 79, n. 1, p. 1, doi. 10.1111/ahg.12093

By:

Kanthimathi, Sekar;
Balamurugan, Kandasamy;
Mohan, Viswanathan;
Shanthirani, Coimbatore Subramaniyam;
Gayathri, Vijay;
Radha, Venkatesan

Publication type:

Article

Consanguinity and Late Fertility: Spatial Analysis Reveals Positive Association Patterns.

Published in:

Annals of Human Genetics, 2015, v. 79, n. 1, p. 1, doi. 10.1111/ahg.12092

By:

Lisa, Antonella;
Astolfi, Paola;
Zei, Gianna;
Tentoni, Stefania

Publication type:

Article

Corrigendum.

Published in:: Annals of Human Genetics, 2015, v. 79, n. 1, p. 83, doi. 10.1111/ahg.12091
Publication type:: Article

Identification of Six Novel Mutations in ZEB1 and Description of the Associated Phenotypes in Patients with Posterior Polymorphous Corneal Dystrophy 3.

Published in:

Annals of Human Genetics, 2015, v. 79, n. 1, p. 1, doi. 10.1111/ahg.12090

By:

Evans, Cerys J.;
Liskova, Petra;
Dudakova, Lubica;
Hrabcikova, Pavlina;
Horinek, Ales;
Jirsova, Katerina;
Filipec, Martin;
Hardcastle, Alison J.;
Davidson, Alice E.;
Tuft, Stephen J.

Publication type:

Article

A Family-Based Joint Test for Mean and Variance Heterogeneity for Quantitative Traits.

Published in:

Annals of Human Genetics, 2015, v. 79, n. 1, p. 1, doi. 10.1111/ahg.12089

By:

Cao, Ying;
Maxwell, Taylor J.;
Wei, Peng

Publication type:

Article

Neurogenetic Disorders in the Basque Population.

Published in:

Annals of Human Genetics, 2015, v. 79, n. 1, p. 1, doi. 10.1111/ahg.12088

By:

Massó, José Félix Martí;
Zarranz, Juan José;
Otaegui, David;
López de Munain, Adolfo

Publication type:

Article

Familial Mediterranean Fever Associated with MEFV Mutations in a Large Cohort of Cypriot Patients.

Published in:

Annals of Human Genetics, 2015, v. 79, n. 1, p. 1, doi. 10.1111/ahg.12087

By:

Neocleous, Vassos;
Costi, Constantina;
Kyriakou, Christina;
Kyriakides, Tassos C;
Shammas, Christos;
Skordis, Nicos;
Toumba, Meropi;
Kyriakou, Sophia;
Koliou, Maria;
Kousparou, Marianna;
Onoufriou, Margarita;
Hadjipanayis, Adamos;
Iasonides, Michalis;
Atamyan, Vick N;
Pierides, Alkis;
Christophidou‐Anastasiadou, Violetta;
Tanteles, George A;
Phylactou, Leonidas A

Publication type:

Article

Autosomal Dominant Hearing Loss resulting from p.R75Q Mutation in the GJB2 Gene: Nonsyndromic presentation in a South Indian Family.

Published in:

Annals of Human Genetics, 2015, v. 79, n. 1, p. 1, doi. 10.1111/ahg.12086

By:

Pavithra, Amritkumar;
Selvakumari, Mathiyalagan;
Nityaa, Venkatesan;
Sharanya, Narasimhan;
Ramakrishnan, Rajagopalan;
Narasimhan, Murali;
Srisailapathy, C.R. Srikumari

Publication type:

Article

The Association between the Polymorphisms in a Sodium Channel Gene SCN7A and Essential Hypertension: A Case-Control Study in the Northern Han Chinese.

Published in:

Annals of Human Genetics, 2015, v. 79, n. 1, p. 1, doi. 10.1111/ahg.12085

By:

Zhang, Bei;
Li, Mei;
Wang, Lijuan;
Li, Chuang;
Lou, Yuqing;
Liu, Jielin;
Liu, Ya;
Wang, Zuoguang;
Wen, Shaojun

Publication type:

Article