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- 2022
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Mark
A new missense variant in exon 7 of the ABO gene, c.662G>A, in a family with B
w phenotype.
(
- Contribution to journal › Article
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Mark
HLA analysis of immune checkpoint inhibitor-induced and idiopathic isolated ACTH deficiency
(
- Contribution to journal › Article
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Mark
Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes
(
- Contribution to journal › Article
- 2021
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Mark
The trans-ancestral genomic architecture of glycemic traits
(
- Contribution to journal › Article
- 2019
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Mark
Genotyping and serotyping profiles showed weak Jka presentation for previously typed as Jknull donors
(
- Contribution to journal › Article
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Mark
Single cell analysis of autism patient with bi-allelic NRXN1-alpha deletion reveals skewed fate choice in neural progenitors and impaired neuronal functionality
(
- Contribution to journal › Article
- 2018
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Mark
Multigene panel testing beyond BRCA1/2 in breast/ovarian cancer Spanish families and clinical actionability of findings
(
- Contribution to journal › Article
- 2017
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Mark
A low-frequency inactivating AKT2 variant enriched in the finnish population is associated with fasting insulin levels and type 2 diabetes risk
(
- Contribution to journal › Article
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Mark
Polymorphisms in ADH1B and ALDH2 genes associated with the increased risk of gastric cancer in West Bengal, India
(
- Contribution to journal › Article
- 2016
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Mark
The genetic architecture of type 2 diabetes
(
- Contribution to journal › Article