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- 2020
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Mark
Two Prevalent ∼100-kb GYPB Deletions Causative of the GPB-Deficient Blood Group MNS Phenotype S-s-U-in Black Africans
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- Contribution to journal › Article
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Mark
Genetic Discrimination Between LADA and Childhood-Onset Type 1 Diabetes Within the MHC
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- Contribution to journal › Article
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Mark
Parental origin of monosomic chromosomes in near-haploid acute lymphoblastic leukemia
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- Contribution to journal › Letter
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Mark
The Xg blood group system : no longer forgotten
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- Contribution to journal › Letter
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Mark
May the FORS be with you : a system sequel
(
- Contribution to journal › Scientific review
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Mark
Association between the rs1544410 polymorphism in the vitamin D receptor (VDR) gene and insulin secretion after gestational diabetes mellitus
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- Contribution to journal › Article
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Mark
Protein-altering germline mutations implicate novel genes related to lung cancer development
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- Contribution to journal › Article
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Mark
Monozygotic twins with myocarditis and a novel likely pathogenic desmoplakin gene variant
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- Contribution to journal › Article
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Mark
An integrative phenotype–genotype approach using phenotypic characteristics from the UAE national diabetes study identifies HSD17B12 as a candidate gene for obesity and type 2 diabetes
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- Contribution to journal › Article
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Mark
Subclonal patterns in follow-up of acute myeloid leukemia combining whole exome sequencing and ultrasensitive IBSAFE digital droplet analysis
(
- Contribution to journal › Article