DNA synthesis of human XYY cells. Autoradiography and fluorescence pattern

Re-evaluation of the dysequilibrium syndrome.

Acta neurologica Scandinavica·2010

Prevalence and associated impairments of mild mental retardation in six- to ten-year old children in Pakistan: a prospective study.

Acta paediatrica (Oslo, Norway : 1992)·2002

Further evidence of genetic homogeneity in Sjögren-Larsson syndrome.

Acta dermato-venereologica·1999

Friedreich's ataxia: point mutations and clinical presentation of compound heterozygotes.

Annals of neurology·1999

Risk factors for mortality in young children living under various socio-economic conditions in Lahore, Pakistan: with particular reference to inbreeding.

Clinical genetics·1998

Clustering of private mutations in the congenital chloride diarrhea/down-regulated in adenoma gene.

Human mutation·1998

Genetic Testing Unveils a Novel Thrombospondin-1 Domain Containing Protein 1 Gene Variant as the Cause of Chronic Edema in a 79-Year-Old Woman.

Clinical genetics·2026

A Novel De Novo STAG1 Variant at the RAD21 Binding Interface Is Associated With Hypoglycemia, Recurrent Fever, Immunodeficiency and Features of Classical Cohesinopathies.

Clinical genetics·2026

Pathogenicity of NUSAP1 Variants Is Defined by NMD-Escape: Evidence From Two Novel Cases and Systematic Population-Based Variant Analysis.

Clinical genetics·2026

Biallelic ABCA13 Loss-of-Function Variants in a Child With Neurodevelopmental Delay: A Case Report.

Clinical genetics·2026

Variants in the Imprinted IGF2 Gene: A Review and Phasing of De Novo Variants Using Long-Read Sequencing.

Clinical genetics·2026

Establishing a Prognosis When Identifying Pathogenic Variants in Usher Syndrome/DFNB-Related Genes: An Impossible Challenge?

Clinical genetics·2026

Applications of Dynamic Online Sample Preconcentration Techniques in Chiral Capillary Electrophoresis.

Electrophoresis·2026

Comparative Performance Analysis of Three Point-of-Care Glucose Testing Devices against a Central Laboratory Reference Method.

EJIFCC·2026

Taming the Halogen Dance of Bromo(Thi)azoles through Flow Microreactors.

The Journal of organic chemistry·2026

Early Donor-Derived Cell-Free DNA Kinetics After Kidney Transplantation in Atypical Hemolytic Uremic Syndrome: A Preliminary Observational Study.

International journal of molecular sciences·2026

Continuous flow titration based on complementary variation of titrant and sample concentrations.

Talanta·2026

Air-stream assisted separation and photometric determination of ethanol in wine using an automated flow system.

Analytical methods : advancing methods and applications·2026

Related Experiment Videos

DNA synthesis of human XYY cells. Autoradiography and fluorescence pattern

Related Concept Videos

Re-evaluation of the dysequilibrium syndrome.

Prevalence and associated impairments of mild mental retardation in six- to ten-year old children in Pakistan: a prospective study.

Further evidence of genetic homogeneity in Sjögren-Larsson syndrome.

Friedreich's ataxia: point mutations and clinical presentation of compound heterozygotes.

Risk factors for mortality in young children living under various socio-economic conditions in Lahore, Pakistan: with particular reference to inbreeding.

Clustering of private mutations in the congenital chloride diarrhea/down-regulated in adenoma gene.

Genetic Testing Unveils a Novel Thrombospondin-1 Domain Containing Protein 1 Gene Variant as the Cause of Chronic Edema in a 79-Year-Old Woman.

A Novel De Novo STAG1 Variant at the RAD21 Binding Interface Is Associated With Hypoglycemia, Recurrent Fever, Immunodeficiency and Features of Classical Cohesinopathies.

Pathogenicity of NUSAP1 Variants Is Defined by NMD-Escape: Evidence From Two Novel Cases and Systematic Population-Based Variant Analysis.

Biallelic ABCA13 Loss-of-Function Variants in a Child With Neurodevelopmental Delay: A Case Report.

Variants in the Imprinted IGF2 Gene: A Review and Phasing of De Novo Variants Using Long-Read Sequencing.

Establishing a Prognosis When Identifying Pathogenic Variants in Usher Syndrome/DFNB-Related Genes: An Impossible Challenge?

Applications of Dynamic Online Sample Preconcentration Techniques in Chiral Capillary Electrophoresis.

Comparative Performance Analysis of Three Point-of-Care Glucose Testing Devices against a Central Laboratory Reference Method.

Taming the Halogen Dance of Bromo(Thi)azoles through Flow Microreactors.

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DNA synthesis of human XYY cells. Autoradiography and fluorescence pattern

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