A comprehensive review of HVS‐I mitochondrial DNA variation of 19 Iranian populations.
- Published in:
- Annals of Human Genetics, 2024, v. 88, n. 3, p. 259, doi. 10.1111/ahg.12544
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- Publication type:
- Article
Works matching IS 00034800 AND DT 2024 AND VI 88 AND IP 3
Results: 6
1
2
Exploring the clinical significance of miR‐148 expression variations in distinct subtypes of irritable bowel syndrome.
- Published in:
- Annals of Human Genetics, 2024, v. 88, n. 3, p. 247, doi. 10.1111/ahg.12543
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- Publication type:
- Article
3
Molecular and computational characterization of ABCB11 and ABCG5 variants in Tunisian patients with neonatal/infantile low‐GGT intrahepatic cholestasis: Genetic diagnosis and genotype–phenotype correlation assessment.
- Published in:
- Annals of Human Genetics, 2024, v. 88, n. 3, p. 194, doi. 10.1111/ahg.12542
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- Publication type:
- Article
4
Expression analysis of NF1‐mutated alleles in a rare compound heterozygous spinal NF1 patient by digital PCR.
- Published in:
- Annals of Human Genetics, 2024, v. 88, n. 3, p. 183, doi. 10.1111/ahg.12540
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- Publication type:
- Article
5
Using the Bayesian variational spike and slab model in a genome‐wide association study for finding associated loci with bipolar disorder.
- Published in:
- Annals of Human Genetics, 2024, v. 88, n. 3, p. 212, doi. 10.1111/ahg.12538
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- Publication type:
- Article
6
Issue Information.
- Published in:
- Annals of Human Genetics, 2024, v. 88, n. 3, p. 1, doi. 10.1111/ahg.12514
- Publication type:
- Article