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Works matching IS 00015652 AND DT 2023 AND VI 88 AND IP 1

Results: 2

1

Reduction of Missed Diagnosis of G6PD Deficiency in Heterozygous Females by G6PD/6PGD Ratio Assay Combined with Amplification Refractory Mutation System PCR.

Published in:

Human Heredity, 2023, v. 88, n. 1, p. 1, doi. 10.1159/000527806

By:

Chen, Shiguo;
Gao, Jian;
Wu, Qunyan;
Li, Xi;
Lin, Sheng;
Su, Jindi;
Zheng, Kaifeng;
Guo, Zhaopeng;
Yao, Jilong;
Duan, Shan

Publication type:

Article

2

A Comprehensive Study of Disease-Causing Variants in PAH, QDPR, PTS, and PCD Genes in Iranian Patients with Hyperphenylalaninemia: A Systematic Review.

Published in:

Human Heredity, 2023, v. 88, n. 1, p. 8, doi. 10.1159/000529037

By:

Ghanei, Mahmoud;
Sadat Fatemi, Seyedeh Helia;
Hamzehlouei, Tayebeh

Publication type:

Article