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Works matching IS 00015652 AND DT 2022 AND VI 87 AND IP 2

Results: 4

1

Identification of CHEK2 Germline Mutations in BRCA1/2- and PALB2-Negative Breast and Ovarian Cancer Patients.

Published in:

Human Heredity, 2022, v. 87, n. 2, p. 21, doi. 10.1159/000521369

By:

Aksoy, Fuat;
Tezcan Unlu, Havva;
Cecener, Gulsah;
Guney Eskiler, Gamze;
Egeli, Unal;
Tunca, Berrin;
Efendi Erdem, Ecem;
Senol, Kazım;
Gokgoz, Mustafa Sehsuvar

Publication type:

Article

2

Identification of a Novel Mutation in Patients with Type A Insulin Resistance Syndrome.

Published in:

Human Heredity, 2022, v. 87, n. 2, p. 60, doi. 10.1159/000525223

By:

Zhao, Liling;
Dai, Hongmei;
Zhang, Qin;
Hu, Wenmu;
Jin, Ping

Publication type:

Article

3

The Mitochondrial tRNA<sup>Asp</sup> T7561C, tRNA<sup>His</sup> C12153T, and A12172G Mutations May Be Associated with Essential Hypertension in a Han Chinese Pedigree.

Published in:

Human Heredity, 2022, v. 87, n. 2, p. 51, doi. 10.1159/000524163

By:

Fu, Haiying;
Sun, Jinming;
Xu, Xiaoyan

Publication type:

Article

4

Genetic Analyses of Enamel Hypoplasia in Multiethnic Cohorts.

Published in:

Human Heredity, 2022, v. 87, n. 2, p. 34, doi. 10.1159/000522642

By:

Alotaibi, Rasha N.;
Howe, Brian J.;
Moreno Uribe, Lina M.;
Sanchez, Carla;
Deleyiannis, Frederic W.B.;
Padilla, Carmencita;
Poletta, Fernando A.;
Orioli, Ieda M.;
Buxó, Carmen J.;
Wehby, George L.;
Vieira, Alexandre R.;
Murray, Jeffrey;
Valencia-Ramírez, Consuelo;
Restrepo Muñeton, Claudia P.;
Long, Ross E.;
Shaffer, John R.;
Reis, Steven E.;
Weinberg, Seth M.;
Neiswanger, Katherine;
McNeil, Daniel W.

Publication type:

Article