Efficacy and Safety of Hypomethylating Agents in Chronic Myelomonocytic Leukemia: A Single-Arm Meta-analysis.
- Published in:
- Global Medical Genetics, 2022, v. 9, n. 2, p. 141, doi. 10.1055/s-0042-1744157
- By:
- Publication type:
- Article
Works matching IS 26999404 AND DT 2022 AND VI 9 AND IP 2
Results: 21
1
2
Comparison of Bioinformatics Approaches for Fetal Microdeletions and Monogenic Variations Estimation in Non-invasive Prenatal Testing.
- Published in:
- Global Medical Genetics, 2022, v. 9, n. 2, p. 72, doi. 10.1055/s-0042-1743573
- By:
- Publication type:
- Article
3
The Human Genetics of Dental Anomalies.
- Published in:
- Global Medical Genetics, 2022, v. 9, n. 2, p. 76, doi. 10.1055/s-0042-1743572
- By:
- Publication type:
- Article
4
A Computational Data Mining Strategy to Identify the Common Genetic Markers of Temporomandibular Joint Disorders and Osteoarthritis.
- Published in:
- Global Medical Genetics, 2022, v. 9, n. 2, p. 159, doi. 10.1055/s-0042-1743571
- By:
- Publication type:
- Article
5
Evaluation of Utilizing the Distinct Genes as Predictive Biomarkers in Late-Onset Alzheimer’s Disease.
- Published in:
- Global Medical Genetics, 2022, v. 9, n. 2, p. 110, doi. 10.1055/s-0042-1743570
- By:
- Publication type:
- Article
6
CD24<sup>+</sup> MDSC-DCs Induced by CCL5-Deficiency Showed Improved Antitumor Activity as Tumor Vaccines.
- Published in:
- Global Medical Genetics, 2022, v. 9, n. 2, p. 97, doi. 10.1055/s-0042-1743569
- By:
- Publication type:
- Article
7
Genotype–Phenotype Correlations for Putative Haploinsufficient Genes in Deletions of 6q26-q27: Report of Eight Patients and Review of Literature.
- Published in:
- Global Medical Genetics, 2022, v. 9, n. 2, p. 166, doi. 10.1055/s-0042-1743568
- By:
- Publication type:
- Article
8
Genetic Variants and Drug Efficacy in Tuberculosis: A Step toward Personalized Therapy.
- Published in:
- Global Medical Genetics, 2022, v. 9, n. 2, p. 90, doi. 10.1055/s-0042-1743567
- By:
- Publication type:
- Article
9
Genetic Variants in Interleukin-10 Gene Association with Susceptibility and Cervical Cancer Development: A Case Control Study.
- Published in:
- Global Medical Genetics, 2022, v. 9, n. 2, p. 129, doi. 10.1055/s-0042-1743262
- By:
- Publication type:
- Article
10
Presentation of an Infant with Chromosome 18p Deletion Syndrome and Asymmetric Septal Hypertrophy.
- Published in:
- Global Medical Genetics, 2022, v. 9, n. 2, p. 179, doi. 10.1055/s-0042-1743261
- By:
- Publication type:
- Article
11
Nucleotide Sequence Sharing between the Human Genome and Primers for Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Detection.
- Published in:
- Global Medical Genetics, 2022, v. 9, n. 2, p. 182, doi. 10.1055/s-0042-1743260
- By:
- Publication type:
- Article
12
Psoriasis: An Immunogenetic Perspective.
- Published in:
- Global Medical Genetics, 2022, v. 9, n. 2, p. 82, doi. 10.1055/s-0042-1743259
- By:
- Publication type:
- Article
13
Mannose-Binding Lectin 2 Gene Polymorphism during Pandemic: COVID-19 Family.
- Published in:
- Global Medical Genetics, 2022, v. 9, n. 2, p. 185, doi. 10.1055/s-0042-1743258
- By:
- Publication type:
- Article
14
Analysis of Genetic Variations in Connexin 26 (GJB2) Gene among Nonsyndromic Hearing Impairment: Familial Study.
- Published in:
- Global Medical Genetics, 2022, v. 9, n. 2, p. 152, doi. 10.1055/s-0042-1743257
- By:
- Publication type:
- Article
15
Determinants in Tailoring Antidiabetic Therapies: A Personalized Approach.
- Published in:
- Global Medical Genetics, 2022, v. 9, n. 2, p. 63, doi. 10.1055/s-0041-1741109
- By:
- Publication type:
- Article
16
A Case of Geroderma Osteodysplasticum Syndrome: Unique Clinical Findings.
- Published in:
- Global Medical Genetics, 2022, v. 9, n. 2, p. 175, doi. 10.1055/s-0041-1740468
- By:
- Publication type:
- Article
17
Molecular Detection of blaOXA-type Carbapenemase Genes and Antimicrobial Resistance Patterns among Clinical Isolates of Acinetobacter baumannii.
- Published in:
- Global Medical Genetics, 2022, v. 9, n. 2, p. 118, doi. 10.1055/s-0041-1740019
- By:
- Publication type:
- Article
18
Phenotype from SAMD9 Mutation at 7p21.2 Appears Attenuated by Novel Compound Heterozygous Variants at RUNX2 and SALL1.
- Published in:
- Global Medical Genetics, 2022, v. 9, n. 2, p. 124, doi. 10.1055/s-0041-1740018
- By:
- Publication type:
- Article
19
Quantitative In Vivo Genetic Analysis Reveals Novel Genetic Determinants of Tumor Initiation, Overall Growth, and Exceptional Growth in KRAS-Driven Lung Cancer.
- Published in:
- 2022
- By:
- Publication type:
- Editorial
20
Genomic and Immunologic Markers of Intrinsic Resistance to PembrolizumabMonotherapy in Microsatellite Instability-High Gastric Cancer: Observations from a Prospective Phase II Study.
- Published in:
- 2022
- By:
- Publication type:
- Editorial
21
Pitfalls of PCR-RFLP in Detecting SARS-CoV-2 D614G Mutation.
- Published in:
- Global Medical Genetics, 2022, v. 9, n. 2, p. 189, doi. 10.1055/s-0041-1735556
- By:
- Publication type:
- Article