Characterization of the beta+-thalassemia mutation in a homozygous Yugoslavian patient

Chromosomal Microarray in Children Born Small for Gestational Age - Single Center Experience.

Balkan journal of medical genetics : BJMG·2025

[Comparison of the efficiency of surgical excision methods for detecting extraprostatic extension and positive resection margin in prostate cancer].

Arkhiv patologii·2023

[Morphological precursors of high-grade serous ovarian cancer].

Arkhiv patologii·2023

Stimulation of Structural and Functional Recovery of the Kidney in Rats with Postischemic Acute Renal Failure of Different Severity by Embryonic Protein-Peptide Complex Therapy.

Bulletin of experimental biology and medicine·2020

[The incidence of AZF deletions, CFTR mutations and long alleles of the ar CAG repeats during the primary laboratory diagnostics in a heterogeneous group of infertily men].

Urologiia (Moscow, Russia : 1999)·2019

Stimulation of Spermatogenesis and Synthesis of Testosterone by Allotransplantation of Neonatal Testicular Tissue under Tunica Albuginea of Cryptorchid Testis.

Bulletin of experimental biology and medicine·2019

Precision Medicine in Sickle Cell Disease: From Molecular Pathways to Curative Strategies.

Hemoglobin·2026

Endocrine Complications in Patients with Congenital Dyserythropoietic Anemia: A Single-Center Cohort Study.

Hemoglobin·2026

Metabolomic and Proteomic Profiling of Vaso-Occlusive Crises in Sickle Cell Disease: Current Evidence and Future Perspectives.

Hemoglobin·2026

Evaluation of a Customized RDB-FTH Panel for β-Globin Variants in a Malaysian Tertiary Center.

Hemoglobin·2026

CRISPR-Based Mediated Reactivation of Fetal Hemoglobin as a Therapeutic Strategy for Hemoglobinopathies: Evidence from Preclinical to Clinical Trials in Sickle Cell Disease and β-Thalassemia.

Hemoglobin·2026

Genotype-Specific Hematologic Signatures Across α-Globin Defect Categories in α-Thalassemia.

Hemoglobin·2026

Sequence diversity and forensic efficiency of Y-STRs in the Han population of Yunnan Province, Southwest China.

International journal of legal medicine·2026

A Novel Homozygous Nonsense Variant in DCHS1 in a Brazilian Patient With Van Maldergem Syndrome Type 1: Clinical Report and Literature Review.

American journal of medical genetics. Part A·2026

Repeat-length variation generates stable TTGGG-family G-quadruplex motifs in plant mitochondrial genomes.

Planta·2026

A KIAA0586 c.1815G>A Founder Allele Associated with Short-Rib Polydactyly Syndrome Type IV in Romani Families.

medRxiv : the preprint server for health sciences·2026

A Microfluidics-Based Assay for the Discovery of Gametogenic Rejuvenation Factors in Saccharomyces cerevisiae.

Journal of visualized experiments : JoVE·2026

Beyond two alleles: multiallelic genotypic selection and its estimation from time-series data.

BMC genomics·2026

Related Experiment Videos

Characterization of the beta+-thalassemia mutation in a homozygous Yugoslavian patient

Related Concept Videos

Chromosomal Microarray in Children Born Small for Gestational Age - Single Center Experience.

[Comparison of the efficiency of surgical excision methods for detecting extraprostatic extension and positive resection margin in prostate cancer].

[Morphological precursors of high-grade serous ovarian cancer].

Stimulation of Structural and Functional Recovery of the Kidney in Rats with Postischemic Acute Renal Failure of Different Severity by Embryonic Protein-Peptide Complex Therapy.

[The incidence of AZF deletions, CFTR mutations and long alleles of the ar CAG repeats during the primary laboratory diagnostics in a heterogeneous group of infertily men].

Stimulation of Spermatogenesis and Synthesis of Testosterone by Allotransplantation of Neonatal Testicular Tissue under Tunica Albuginea of Cryptorchid Testis.

Precision Medicine in Sickle Cell Disease: From Molecular Pathways to Curative Strategies.

Endocrine Complications in Patients with Congenital Dyserythropoietic Anemia: A Single-Center Cohort Study.

Metabolomic and Proteomic Profiling of Vaso-Occlusive Crises in Sickle Cell Disease: Current Evidence and Future Perspectives.

Evaluation of a Customized RDB-FTH Panel for β-Globin Variants in a Malaysian Tertiary Center.

CRISPR-Based Mediated Reactivation of Fetal Hemoglobin as a Therapeutic Strategy for Hemoglobinopathies: Evidence from Preclinical to Clinical Trials in Sickle Cell Disease and β-Thalassemia.

Genotype-Specific Hematologic Signatures Across α-Globin Defect Categories in α-Thalassemia.

Sequence diversity and forensic efficiency of Y-STRs in the Han population of Yunnan Province, Southwest China.

A Novel Homozygous Nonsense Variant in DCHS1 in a Brazilian Patient With Van Maldergem Syndrome Type 1: Clinical Report and Literature Review.

Repeat-length variation generates stable TTGGG-family G-quadruplex motifs in plant mitochondrial genomes.

A KIAA0586 c.1815G>A Founder Allele Associated with Short-Rib Polydactyly Syndrome Type IV in Romani Families.

A Microfluidics-Based Assay for the Discovery of Gametogenic Rejuvenation Factors in Saccharomyces cerevisiae.

Beyond two alleles: multiallelic genotypic selection and its estimation from time-series data.

Related Experiment Videos

Characterization of the beta+-thalassemia mutation in a homozygous Yugoslavian patient

Related Concept Videos

Related Articles