GeneralConnection.com ➔ Dictionary
Dictionary Search

heterozygous

Synonyms

Adjective

1. heterozygous

Usage
Clinico-Hematological Profile of Double Heterozygous Hemoglobinopathies Diagnosed by High-Performance Liquid Chromatography: A Cross-Sectional Study - Cureus
In vivo base editing gene therapy for heterozygous familial hypercholesterolemia: a phase 1 trial - Nature
Five children with haploinsufficiency of A20 caused by heterozygous mutations in the TNFAIP3 gene - Frontiers
Genetically heterozygous - transcriptionally homozygous IRF7 deficiency underlies herpesvirus CNS infections in humans - Rockefeller University Press
Expanding the Early Childhood Manifestations of ITPR1 Heterozygous Variants Beyond Congenital Ataxia and Gillespie Syndrome - Neurology® Journals
Setmelanotide fails to lower BMI in patients with heterozygous genes tied to obesity - Healio
Extensive heterozygosity and genetic exchange among natural populations of Leishmania species - PNAS
Chromosome-level haplotype-resolved assembly of highly heterozygous grass genomes with PhaseGrass - Nature
A novel heterozygous pathogenic AIRE variant causing autoimmunity but not infectious susceptibility - Rockefeller University Press
A Diagnostic Conundrum: Atypical McArdle Disease Mimic With Heterozygous PYGM Mutation and Cytochrome C Oxidase (COX)-Negative Fibers - Cureus
Progressive encephalopathy associated with novel compound heterozygous NAXE mutations in a Chinese patient: case report and literature review - Frontiers
A novel compound heterozygous YY1AP1 variant in Grange syndrome: importance of early signs in preventing life-threatening vascular complications - Nature
Dominant negative ADA2 mutations cause ADA2 deficiency in heterozygous carriers - Rockefeller University Press
Compound Heterozygous Hemoglobin E-Beta (HbE-β)-Thalassemia Presenting With Chipmunk or Rodent Facies, and a Severe Thalassemia Major Phenotype - Cureus
Sustained HIV-1 remission after heterozygous CCR5Δ32 stem cell transplantation - Nature
Novel Compound Heterozygous CFAP53 Variants in a Fetus With Situs Inversus Totalis: A Case Report - Cureus
Heterozygous frameshift KMT2A variant in a patient with Wiedemann–Steiner syndrome - Nature
Enhancing local meiotic crossovers in Arabidopsis and maize through juxtaposition of heterozygous and homozygous regions - Nature
Compound heterozygous variants of CACNA1H change channel properties and contribute to intractable epilepsy with myoclonic-atonic seizures - Nature
Differential phenotypes in mice with smooth muscle-specific heterozygous versus homozygous deletion of Stk11 - Nature
Heterozygous LKB1 Loss Induces Premalignant Regenerative State in Intestinal Epithelium, Promoting Serrated Colorectal Cancer Risk in Peutz-Jeghers Syndrome - Vera Health
Mutation Induces Epileptiform Activity and Multiple Behavioral Abnormalities in Heterozygous Knock-in Mice - Journal of Neuroscience
Isoform analysis of heterozygous putative splicing variants at the allele level using nanopore long-read sequencing - Nature
Case Report: Compound heterozygous familial hypercholesterolemia in a pediatric patient with multiple cutaneous xanthomas - Frontiers
HIV Remission with Allo-SCT Endures in Heterozygous CCR5Δ32 Patient - Inside Precision Medicine
Case report: Compound Heterozygous Mutations in the IDUA Gene Causing Mucopolysaccharidosis Type I with Uterine Developmental Abnormality - Frontiers
Compound Heterozygous Sickle Cell-Beta Thalassemia Presenting As Chronic Hemolytic Anemia With Microcytosis and Prominent Left Ventricular Trabeculation: A Case Report - Cureus
A heterozygous 9q34 deletion encompassing SPTAN1 as a cause of distal myopathy - Nature
Diversity favoured: heterozygosity attracts crossovers - Nature
BRAT1 gene compound heterozygous mutations causing lethal neonatal rigidity and multifocal seizure syndrome: a case report - Frontiers
Compound Heterozygous Protein C Deficiency Presenting With Splenic Infarction After COVID-19: A Case Report - Cureus
Heterozygous PRDM9 truncating variant in a patient with primary ovarian insufficiency | Journal of Human Genetics - Nature
Case Report: Novel compound heterozygous mutations in PNPLA6 gene associated with Oliver-McFarlane syndrome - Frontiers
HIV remission after heterozygous CCR5Δ32 stem cell transplant - BioWorld News
A Rare Heterozygous MYH11 Missense Variant in a Patient With Recurrent Strokes, Intracerebral Arterial Pathology, and Aortic Aneurysm - Cureus
FDA Approves Lerodalcibep for Hypercholesterolemia and Heterozygous Familial Hypercholesterolemia - Pharmacy Times
Coronary artery bypass grafting in a 14-year-old boy with compound heterozygous LDLR familial hypercholesterolemia: a case report - Frontiers
Uncovering compound heterozygous DYSF variants in a Chinese family affected by limb-girdle muscular dystrophy type 2B - Frontiers
Dr. Roach: Explaining the science behind having the factor V Leiden gene - The Detroit News
Novel compound heterozygous MRTFA gene variants cause multiple dysfunctions of neutrophils and autoinflammation - Wiley Online Library
Novel PCSK9 Inhibitor Recaticimab Lowers LDL-C in Adult Heterozygous Familial Hypercholesterolemia - Pharmacy Times
Compound heterozygous mutations in MICU1 cause myopathy with extrapyramidal signs in two Chinese pedigrees - Frontiers
Apparent Nonresponse to PCSK9 Inhibition in a Patient With Heterozygous Familial Hypercholesterolemia Due to PCSK9 Gene Duplication: - JACC Journals
Case report and literature review: novel TXNRD2 compound heterozygous variants in familial glucocorticoid deficiency type 5 - Frontiers
Menarini Group's Obicetrapib and Obicetrapib/Ezetimibe Marketing Authorisation Applications Accepted for Review by the European Medicines Agency (EMA) for the Treatment of adults with primary hypercholesterolaemia (heterozygous familial and non-famil - PR Newswire
Heterozygous familial hypercholesterolemia: PCSK9 inhibition lowers LDL-C regardless of LDLR variant function - Vera Health
A case of coexisting heterozygous NOTCH3 and HTRA1 mutations in cerebral small vessel disease - Nature
A new neurodevelopmental disorder linked to heterozygous variants in UNC79. - Physician's Weekly
Dadaism catches up with DADA2 - Rockefeller University Press
Phenotypic complexities of rare heterozygous neurexin-1 deletions - Nature
Resilience to autosomal dominant Alzheimer’s disease in a Reelin-COLBOS heterozygous man - Nature
Coupling metabolomics and exome sequencing reveals graded effects of rare damaging heterozygous variants on gene function and human traits - Nature
Effect of heterozygous deletions on phenotypic changes and dosage compensation in Arabidopsis thaliana - Nature
Heterozygous knockout of Synaptotagmin13 phenocopies ALS features and TP53 activation in human motor neurons - Nature
Heterozygous ABCG5 Gene Deficiency and Risk of Coronary Artery Disease - American Heart Association Journals
Heterozygous de novo dominant negative mutation of REXO2 results in interferonopathy - Nature
Hematopoietic-specific heterozygous loss of Dnmt3a exacerbates colitis-associated colon cancer - Rockefeller University Press
Inducing multiple nicks promotes interhomolog homologous recombination to correct heterozygous mutations in somatic cells - Nature
Two divergent haplotypes from a highly heterozygous lychee genome suggest independent domestication events for early and late-maturing cultivars - Nature
Haplotype-resolved genome analyses of a heterozygous diploid potato - Nature
Inclisiran for the Treatment of Heterozygous Familial Hypercholesterolemia - The New England Journal of Medicine
Heterozygous missense variant of the proteasome subunit β-type 9 causes neonatal-onset autoinflammation and immunodeficiency - Nature
Production of a heterozygous exon skipping model of common marmosets using gene-editing technology | Lab Animal - Nature
Efficient introduction of specific homozygous and heterozygous mutations using CRISPR/Cas9 - Nature
Compound heterozygous mutations in TGFBI cause a severe phenotype of granular corneal dystrophy type 2 - Nature
Case report: A novel compound heterozygous variant in the COL4A3 gene was identified in a patient with autosomal recessive Alport syndrome - Frontiers
Heterozygous variants in GATA2 contribute to DCML deficiency in mice by disrupting tandem protein binding - Nature
Heterozygous variants disrupting the interaction of ERF with activated ERK1/2 cause microcephaly, developmental delay, and skeletal anomalies - Nature
Heterozygous RFX6 protein truncating variants are associated with MODY with reduced penetrance - Nature
Not just a carrier: Clinical presentation and management of patients with heterozygous disease‐causing alkaline phosphatase (ALPL) variants identified through expanded carrier screening - Wiley Online Library
Rare heterozygous variants in paediatric steroid resistant nephrotic syndrome – a population-based analysis of their significance - Nature
A Survey of Compound Heterozygous Variants in Pediatric Cancers and Structural Birth Defects - Frontiers
Evolocumab in Pediatric Heterozygous Familial Hypercholesterolemia - The New England Journal of Medicine
Heterozygous diploid and interspecies SCRaMbLEing - Nature
Heterozygous missense variant in GLI2 impairs human endocrine pancreas development - Nature
Novel compound heterozygous ABCA2 variants cause IDPOGSA, a variable phenotypic syndrome with intellectual disability | Journal of Human Genetics - Nature
Genomic insights into selection for heterozygous alleles and woody traits in Populus tomentosa - Wiley Online Library
A Rare Case of Heterozygous C282Y Mutation Causing Hereditary Hemochromatosis With Acute Pancreatitis - Cureus
Transcriptomic and epigenomic consequences of heterozygous loss-of-function mutations in AKAP11, a shared risk gene for bipolar disorder and schizophrenia | Molecular Psychiatry - Nature
Genetic screening confirms heterozygous mutations in ACAN as a major cause of idiopathic short stature - Nature
Heterozygous BTNL8 variants in individuals with multisystem inflammatory syndrome in children (MIS-C) - Rockefeller University Press
Novel MYH10 heterozygous variants associated to a syndrome combining mainly ptosis and ocular coloboma expand the MYH10 related phenotypes | European Journal of Human Genetics - Nature
Heterozygous deletion of chromosome 17p renders prostate cancer vulnerable to inhibition of RNA polymerase II - Nature
Characterization of heterozygosity-rich regions in Italian and worldwide goat breeds - Nature
Cas9-mediated allelic exchange repairs compound heterozygous recessive mutations in mice - Nature
Compound heterozygous mutations in a mouse model of Leber congenital amaurosis reveal the role of CCT2 in photoreceptor maintenance - Nature
Genome-wide single nucleotide polymorphism array analysis unveils the origin of heterozygous androgenetic complete moles - Nature
Molecular phenotypes of mitochondrial dysfunction in clinically non-manifesting heterozygous PRKN variant carriers - Nature
Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease - Rockefeller University Press
Estimating the selective effects of heterozygous protein-truncating variants from human exome data - Nature
The mutagenic chain reaction: A method for converting heterozygous to homozygous mutations - Science | AAAS
Loss of B Cells in Patients with Heterozygous Mutations in IKAROS - The New England Journal of Medicine
Cerebral arteriopathy associated with heterozygous variants in the casitas B-lineage lymphoma gene - Neurology® Journals
Compound heterozygous variants of THG1L result in autosomal recessive cerebellar ataxia - Nature
Rare heterozygous GDF6 variants in patients with renal anomalies - Nature
Double heterozygous pathogenic mutations in KIF3C and ZNF513 cause hereditary gingival fibromatosis - Nature
A novel heterozygous mutation of ANKRD11 causes KBG syndrome in a preterm neonate: a case report and literature review - Frontiers
Inferring compound heterozygosity from large-scale exome sequencing data - Nature
Heterozygous mutations cause genetic instability in a yeast model of cancer evolution - Nature
Double heterozygous pathogenic variants prevalence in a cohort of patients with hereditary breast cancer - Frontiers
Foreign Language Equivalents
Foreign Language Equivalents of 'heterozygous'
Language Equivalent   Language Equivalent
French    Spanish
Misspellings - Typos
hetrrozygous,   hteerozygous,   hetorozygous,   heterzygous,   ehterozygous,   heteroygous,   heterozyous,   heyerozygous,   heteroyzgous,   heterozgyous,   heterrozygous,   geterozygous,   hwterozygous,   heteroxygous,   heterozygouss,   heteeozygous,   heterozyggous,   heeterozygous,   hetterozygous,   heteroztgous,   hetetozygous,   hetrozygous,   hetreozygous,   heteozygous,   heteorzygous,   heterozygou,   heerozygous,   heterizygous,   hetwrozygous,   heterozyguos,   hterozygous,   heterozygos,   heterozygois,   heterpzygous,   heterozugous,   heterozyfous,   jeterozygous,   eterozygous,   heterozygosu,   heterozygius,   heteroozygous,   heterozygpus,   heterozgous,   hheterozygous,   heterozyhous,   heterozygoous,   heterozygouus,   heterozygoua,   heterozygoud,   heterzoygous,   heterozyogus,   heterozygoys,   hererozygous,   heetrozygous,   hrterozygous,   heterozzygous,   heterozygus,   heteerozygous,   heterozyygous
Words Starting with Letter - 'A'
a a battery a billion
a bit a bit much a capella singing
a cappella singing a couple of a few
a fortiori a good deal a great deal
a horizon a hundred a hundred and one
a hundred thousand a hundred times a kempis
a la carte a la mode a level
a little a lot a million
Go to Page 1              Go to Page 2 »   
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z