Mental retardation of genetic origin in general practice

Prioritising in a crisis: what next for malaria research?

Malaria journal·2026

Impact of atmospheric dust on phytoplankton dynamics and primary productivity in the tropical marine ecosystem of the Eastern Arabian Sea.

Marine pollution bulletin·2025

A critical review on ocean acidification driven by disinfection by-products discharge from ships' ballast water management systems: Impacts on carbon chemistry.

Marine pollution bulletin·2025

Neuro-Behçet's presentation as cerebral venous thrombosis - A report of two cases and review of the literature.

Journal of postgraduate medicine·2024

Oppositional Cat Swarm Optimization-Based Feature Selection Approach for Credit Card Fraud Detection.

Computational intelligence and neuroscience·2023

Microbiome digital signature of MCR genes - an in silico approach to study the diversity of methanogenic population in laboratory-developed and pilot-scale anaerobic digesters.

Access microbiology·2020

Gynandroblastoma: a rare ovarian tumour with an unusual clinical presentation.

Journal of the Indian Medical Association·2015

Bilateral hip and knee arthroplasty in ochronotic arthritis.

Journal of the Indian Medical Association·2015

Biliary colic with dilated common bile duct: simple "sheepish" problem?

Journal of the Indian Medical Association·2015

Proximal femoral focal deficiency revisited: a case report.

Journal of the Indian Medical Association·2015

Disseminated intra-abdominal hydatid disease: surgical management.

Journal of the Indian Medical Association·2015

Eosinophilic ascitis, an unusual presentation of eosinophilic gastro-enteritis.

Journal of the Indian Medical Association·2015

Molecular characterization of FAM222B as a novel disease gene for dominant cardiovascular laterality defects.

Scientific reports·2026

Genetic architecture and inheritance patterns of Leber hereditary optic neuropathy among 419 Chinese pedigrees carrying the ND4 11778G>A mutation.

Journal of genetics and genomics = Yi chuan xue bao·2026

Integrating LNA-qPCR and full-length SMN1 sequencing for precision SMA carrier screening: large-scale validation in 30,849 individuals.

Clinica chimica acta; international journal of clinical chemistry·2026

Novel splice site variants in GBA1 are associated with Gaucher disease and genotype-phenotype correlations.

Brain & development·2026

High-Resolution Physical Mapping and Chromosomal Transmission in Sugarcane Progeny.

The Journal of heredity·2026

Loci Associated With Susceptibility to Biliary Atresia-A Genome-Wide Association Study in Taiwan.

Pediatrics international : official journal of the Japan Pediatric Society·2026

Related Experiment Videos

Mental retardation of genetic origin in general practice

Related Concept Videos

Prioritising in a crisis: what next for malaria research?

Impact of atmospheric dust on phytoplankton dynamics and primary productivity in the tropical marine ecosystem of the Eastern Arabian Sea.

A critical review on ocean acidification driven by disinfection by-products discharge from ships' ballast water management systems: Impacts on carbon chemistry.

Neuro-Behçet's presentation as cerebral venous thrombosis - A report of two cases and review of the literature.

Oppositional Cat Swarm Optimization-Based Feature Selection Approach for Credit Card Fraud Detection.

Microbiome digital signature of MCR genes - an in silico approach to study the diversity of methanogenic population in laboratory-developed and pilot-scale anaerobic digesters.

Gynandroblastoma: a rare ovarian tumour with an unusual clinical presentation.

Bilateral hip and knee arthroplasty in ochronotic arthritis.

Biliary colic with dilated common bile duct: simple "sheepish" problem?

Proximal femoral focal deficiency revisited: a case report.

Disseminated intra-abdominal hydatid disease: surgical management.

Eosinophilic ascitis, an unusual presentation of eosinophilic gastro-enteritis.

Molecular characterization of FAM222B as a novel disease gene for dominant cardiovascular laterality defects.

Genetic architecture and inheritance patterns of Leber hereditary optic neuropathy among 419 Chinese pedigrees carrying the ND4 11778G>A mutation.

Integrating LNA-qPCR and full-length SMN1 sequencing for precision SMA carrier screening: large-scale validation in 30,849 individuals.

Novel splice site variants in GBA1 are associated with Gaucher disease and genotype-phenotype correlations.

High-Resolution Physical Mapping and Chromosomal Transmission in Sugarcane Progeny.

Loci Associated With Susceptibility to Biliary Atresia-A Genome-Wide Association Study in Taiwan.

Related Experiment Videos

Mental retardation of genetic origin in general practice

Related Concept Videos

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