IJMS | Free Full-Text | Derived Polymorphic Amplified Cleaved Sequence (dPACS): A Novel PCR-RFLP Procedure for Detecting Known Single Nucleotide and Deletion–Insertion Polymorphisms | HTML
Frontiers | Locating a novel autosomal recessive genetic variant in the cattle glucokinase gene using only WGS data from three cases and six carriers
PDF) Analysis of reninangiotensin aldosterone system gene polymorphisms in Malaysian essential hypertensive and type 2 diabetic subjects
Protein Encoded by the AxinFu Allele Effectively Down-regulates Wnt Signaling but Exerts a Dominant Negative Effect on c-Jun N-terminal Kinase Signaling* - Journal of Biological Chemistry
Neighboring genes for DNA-binding proteins rescue male sterility in Drosophila hybrids | PNAS
CRISPR-Directed Therapeutic Correction at the NCF1 Locus Is Challenged by Frequent Incidence of Chromosomal Deletions: Molecular Therapy - Methods & Clinical Development
![Indirect proof of principle on c.1213+5G>T [IVS6+5G>T] pathogenicity.... | Download Scientific Diagram](https://www.researchgate.net/publication/338733548/figure/fig3/AS:849987596476417@1579664243721/Indirect-proof-of-principle-on-c1213-5GT-IVS6-5GT-pathogenicity-Electropherograms.jpg "Indirect proof of principle on c.1213+5G>T [IVS6+5G>T] pathogenicity.... | Download Scientific Diagram")
Indirect proof of principle on c.1213+5G>T [IVS6+5G>T] pathogenicity.... | Download Scientific Diagram
Pedigrees of the families and genetic sequencing findings. (A) The... | Download Scientific Diagram
Frontiers | Case report: FOXP1 syndrome caused by a de novo splicing variant (c.1652+5 G>A) of the FOXP1 gene
AAB - Variation in the stearoyl-CoA desaturase gene (SCD) and its influence on milk fatty acid composition in late-lactation dairy cattle grazed on pasture
Homozygous vs Heterozygous Genotype - YouTube
Novel Homozygous Nonsense Mutation Associated with Bardet-Biedl Syndrome in Fetus with Congenital Renal Malformation
Frontiers | Case Report: Complete Maternal Uniparental Disomy of Chromosome 2 With a Novel UNC80 Splicing Variant c.5609-4G> A in a Chinese Patient With Infantile Hypotonia With Psychomotor Retardation and Characteristic Facies
Genotype and allele frequency distribution among hypertensives and controls | Download Scientific Diagram
Vascular pathology to vascular dementia is it multifactorial or due to still unknown factors?
INTRODUCTION
Novel Point Mutations of CITED2 Gene Are Associated with Non-familial Congenital Heart Disease (CHD) in Sporadic Pediatric Patients | SpringerLink
![Associations between the rs5498 (A > G) and rs281432 (C > G) polymorphisms of the ICAM1 gene and atherosclerotic cardiovascular disease risk, including hypercholesterolemia [PeerJ]](https://dfzljdn9uc3pi.cloudfront.net/2022/12972/1/fig-1-2x.jpg "Associations between the rs5498 (A > G) and rs281432 (C > G) polymorphisms of the ICAM1 gene and atherosclerotic cardiovascular disease risk, including hypercholesterolemia [PeerJ]")
Associations between the rs5498 (A > G) and rs281432 (C > G) polymorphisms of the ICAM1 gene and atherosclerotic cardiovascular disease risk, including hypercholesterolemia [PeerJ]
IJMS | Free Full-Text | Molecular Mechanism of Autosomal Recessive Long QT-Syndrome 1 without Deafness | HTML
Genetic factors contributing to hypertension in African‐based populations: A systematic review and meta‐analysis - Yako - 2018 - The Journal of Clinical Hypertension - Wiley Online Library
Oligogenic heterozygous inheritance of sperm abnormalities in mouse | eLife
Frontiers | A Heterozygous LMF1 Gene Mutation (c.1523C>T), Combined With an LPL Gene Mutation (c.590G>A), Aggravates the Clinical Symptoms in Hypertriglyceridemia
Frequency distribution of cytokine and associated transcription factor single nucleotide polymorphisms in Zimbabweans: Impact on schistosome infection and cytokine levels | PLOS Neglected Tropical Diseases
Allele vs Genotype vs Haplotype and More | IDT
