Normal rate of sister chromatid exchange in Down syndrome

[Clinical phenotypic and genotypic analysis of 5 pediatric patients with β-ketothiolase deficiency].

Zhonghua er ke za zhi = Chinese journal of pediatrics·2023

[BCS1Neonatal growth retardation and lactic acidosis initiated by novel mutation sites in L gene].

Zhonghua yu fang yi xue za zhi [Chinese journal of preventive medicine]·2023

Thigh muscle volume predicted by anthropometric measurements and correlated with physical function in the older adults.

The journal of nutrition, health & aging·2011

Unusual manifestations of vertebral osteomyelitis: intraosseous lesions mimicking metastases.

AJNR. American journal of neuroradiology·2008

Childhood obesity, gender, actual-ideal body image discrepancies, and physical self-concept in Hong Kong children: cultural differences in the value of moderation.

Developmental psychology·2007

Cytokine gene polymorphisms in Chinese patients with psoriasis.

The British journal of dermatology·2007

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

Liver disease reveals KIF12 as a regulator of mitochondria, lysosome and cilia localisation in human cholangiocytes.

EBioMedicine·2026

Transgenerational chromosome repair in the asexual bdelloid rotifer Adineta vaga.

Science advances·2026

Site-Specific Measurement of Meiotic Crossing-Over Rate with Droplet Digital PCR.

Cold Spring Harbor protocols·2026

The periphery of nuclear speckles defines a spatially and temporally regulated compartment of long-lived intron-retained RNAs that resolves during mitosis.

Nature cell biology·2026

Whole-genome sequencing identifies a c.1282C > T missense variant in Taurine Transporter (TauT) associated with taurine-mediated dilated cardiomyopathy in a family of domestic shorthair cats.

Journal of molecular and cellular cardiology·2026

Mitochondrial genome characteristics and phylogenetic analysis of Ramaria longispora.

Mitochondrial DNA. Part B, Resources·2026

Related Experiment Videos

Normal rate of sister chromatid exchange in Down syndrome

Related Concept Videos

[Clinical phenotypic and genotypic analysis of 5 pediatric patients with β-ketothiolase deficiency].

[BCS1Neonatal growth retardation and lactic acidosis initiated by novel mutation sites in L gene].

Thigh muscle volume predicted by anthropometric measurements and correlated with physical function in the older adults.

Unusual manifestations of vertebral osteomyelitis: intraosseous lesions mimicking metastases.

Childhood obesity, gender, actual-ideal body image discrepancies, and physical self-concept in Hong Kong children: cultural differences in the value of moderation.

Cytokine gene polymorphisms in Chinese patients with psoriasis.

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?

Liver disease reveals KIF12 as a regulator of mitochondria, lysosome and cilia localisation in human cholangiocytes.

Transgenerational chromosome repair in the asexual bdelloid rotifer Adineta vaga.

Site-Specific Measurement of Meiotic Crossing-Over Rate with Droplet Digital PCR.

The periphery of nuclear speckles defines a spatially and temporally regulated compartment of long-lived intron-retained RNAs that resolves during mitosis.

Whole-genome sequencing identifies a c.1282C > T missense variant in Taurine Transporter (TauT) associated with taurine-mediated dilated cardiomyopathy in a family of domestic shorthair cats.

Mitochondrial genome characteristics and phylogenetic analysis of Ramaria longispora.

Related Experiment Videos

Normal rate of sister chromatid exchange in Down syndrome

Related Concept Videos

Related Articles