Works matching IS 00015652 AND DT 2022 AND VI 87 AND IP 2
Results: 4
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
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- Article
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.
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- Human Heredity, 2022, v. 87, n. 2, p. 51, doi. 10.1159/000524163
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- Article
Genetic Analyses of Enamel Hypoplasia in Multiethnic Cohorts.
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- Human Heredity, 2022, v. 87, n. 2, p. 34, doi. 10.1159/000522642
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- Article
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
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- Article