Preconception genetic diagnosis of cystic fibrosis

The equine graying with age mutation of the STX17 gene: A copy number study using droplet digital PCR reveals a new pattern.

Animal genetics·2021

[Comparative study of the treatment of subtrochanteric fractures in elderly patients: reconstruction nail T2 vs long Gamma nail].

Acta ortopedica mexicana·2021

Staphylococcal Enterotoxins and Toxic Shock Syndrome Toxin-1 (TSST-1) Production During Induced Goat Mastitis.

Journal of food protection·2019

Noncontiguous operon is a genetic organization for coordinating bacterial gene expression.

Proceedings of the National Academy of Sciences of the United States of America·2019

TBX3 and ASIP genotypes reveal discrepancies in officially recorded coat colors of Hucul horses.

Animal : an international journal of animal bioscience·2019

Elemental changes of hippocampal formation occurring during postnatal brain development.

Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements (GMS)·2018

Most-favoured-nation pricing for prescription drugs in US Medicare: a cohort study.

Lancet (London, England)·2026

Immunogenicity of fractional one-fifth and one-half doses of 17DD yellow fever vaccine compared with full dose in children aged 9-23 months in Uganda: a phase 4, single-blind, randomised clinical trial.

Lancet (London, England)·2026

Efficacy and safety of mitapivat in adults with transfusion-dependent α-thalassaemia or β-thalassaemia (ENERGIZE-T): a double-blind, randomised, multicentre, placebo-controlled, phase 3 trial.

Lancet (London, England)·2026

Perioperative durvalumab plus fluorouracil, leucovorin, oxaliplatin, and docetaxel for resectable gastric and gastro-oesophageal junction adenocarcinoma (MATTERHORN): final results of overall survival and event-free survival by pathological response in a global, randomised, double-blind, placebo-controlled, multicentre, phase 3 trial.

Lancet (London, England)·2026

A Normal Phenotype Case of a Small Supernumerary Marker Chromosome Chimeric Carrier with 12p11.21p11.21 Duplication.

Clinical laboratory·2026

Audiological Features in Pendred Syndrome: A Scoping Review.

The journal of international advanced otology·2026

Synergistic Interaction Between PEAR1-FGB and the Dominant Role of ABCB1 in Thrombosis Risk: A SHAP and MDR-Based Study in Vietnamese Pedigrees.

Journal of blood medicine·2026

Mitochondrial Function-Related Genes in Sleep Disorders: A Multi-Omics Mendelian Randomization Study.

Journal of molecular neuroscience : MN·2026

Xp21 contiguous gene deletion syndrome presenting as congenital adrenal hypoplasia: molecular diagnosis and clinical re-evaluation of a pedigree.

Frontiers in endocrinology·2026

Multi-trait GWAS identifies pleiotropic loci shared between early pregnancy bleeding and psychiatric traits.

Frontiers in psychiatry·2026

Related Experiment Videos

Preconception genetic diagnosis of cystic fibrosis

Related Concept Videos

The equine graying with age mutation of the STX17 gene: A copy number study using droplet digital PCR reveals a new pattern.

[Comparative study of the treatment of subtrochanteric fractures in elderly patients: reconstruction nail T2 vs long Gamma nail].

Staphylococcal Enterotoxins and Toxic Shock Syndrome Toxin-1 (TSST-1) Production During Induced Goat Mastitis.

Noncontiguous operon is a genetic organization for coordinating bacterial gene expression.

TBX3 and ASIP genotypes reveal discrepancies in officially recorded coat colors of Hucul horses.

Elemental changes of hippocampal formation occurring during postnatal brain development.

Most-favoured-nation pricing for prescription drugs in US Medicare: a cohort study.

Immunogenicity of fractional one-fifth and one-half doses of 17DD yellow fever vaccine compared with full dose in children aged 9-23 months in Uganda: a phase 4, single-blind, randomised clinical trial.

Efficacy and safety of mitapivat in adults with transfusion-dependent α-thalassaemia or β-thalassaemia (ENERGIZE-T): a double-blind, randomised, multicentre, placebo-controlled, phase 3 trial.

A Normal Phenotype Case of a Small Supernumerary Marker Chromosome Chimeric Carrier with 12p11.21p11.21 Duplication.

Audiological Features in Pendred Syndrome: A Scoping Review.

Synergistic Interaction Between PEAR1-FGB and the Dominant Role of ABCB1 in Thrombosis Risk: A SHAP and MDR-Based Study in Vietnamese Pedigrees.

Mitochondrial Function-Related Genes in Sleep Disorders: A Multi-Omics Mendelian Randomization Study.

Xp21 contiguous gene deletion syndrome presenting as congenital adrenal hypoplasia: molecular diagnosis and clinical re-evaluation of a pedigree.

Multi-trait GWAS identifies pleiotropic loci shared between early pregnancy bleeding and psychiatric traits.

Related Experiment Videos

Preconception genetic diagnosis of cystic fibrosis

Related Concept Videos

Related Articles