Works matching IS 00034800 AND DT 2022 AND VI 86 AND IP 6
Results: 7
Study of variants in genes implicated in rare familial migraine syndromes and their association with migraine in 200,000 exome‐sequenced UK Biobank participants.
- Published in:
- Annals of Human Genetics, 2022, v. 86, n. 6, p. 353, doi. 10.1111/ahg.12484
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- Publication type:
- Article
A novel splicing variant in GALNS in mucopolysaccharidosis IVA and the necessity of re‐evaluating primer sequences.
- Published in:
- Annals of Human Genetics, 2022, v. 86, n. 6, p. 361, doi. 10.1111/ahg.12483
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- Article
Germline variants screening of MLH1, MSH2, MSH6 and PMS2 genes in 64 Algerian Lynch syndrome families: The first nationwide study.
- Published in:
- Annals of Human Genetics, 2022, v. 86, n. 6, p. 328, doi. 10.1111/ahg.12482
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- Publication type:
- Article
Applicability of the IrisPlex system for eye color prediction in an admixed population from Argentina.
- Published in:
- Annals of Human Genetics, 2022, v. 86, n. 6, p. 297, doi. 10.1111/ahg.12480
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- Article
A splice site variant in TCTN3 underlies an atypical form of orofaciodigital syndrome IV.
- Published in:
- Annals of Human Genetics, 2022, v. 86, n. 6, p. 291, doi. 10.1111/ahg.12462
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- Article
Issue Information.
- Published in:
- Annals of Human Genetics, 2022, v. 86, n. 6, p. i, doi. 10.1111/ahg.12435
- Publication type:
- Article
Retraction Statement: Inhibition of miR‐499‐5p expression improves nonalcoholic fatty liver disease.
- Published in:
- Annals of Human Genetics, 2022, v. 86, n. 6, p. 369, doi. 10.1111/ahg.12374
- Publication type:
- Article