Clinical genetics conference: progress in understanding muscle disease

Ribosomal RNA gene sequences and hominoid phylogeny.

Molecular biology and evolution·1990

Sequence and structure correlation of human ribosomal transcribed spacers.

Journal of molecular biology·1990

Human ribosomal DNA: novel sequence organization in a 4.5-kb region upstream from the promoter.

Gene·1989

The role of cytologic NOR variants in the etiology of trisomy 21.

American journal of human genetics·1989

Human 28S ribosomal RNA sequence heterogeneity.

Nucleic acids research·1988

ASHG activities relative to education: Human genetics as a component of medical school curricula: A report to the American society of human genetics.

American journal of human genetics·1988

Does Timing Matter? A Clinical Trial of Supporting Play Exploration and Early Development Intervention (SPEEDI) for Infants Born Preterm in the First Months of Life.

The Journal of pediatrics·2026

Housing Insecurity Among Children of Incarcerated Parents in the United States.

The Journal of pediatrics·2026

Meningococcal B Vaccination Patterns Across 10 Integrated Health Systems within Vaccine Safety Datalink, 2015-2023.

The Journal of pediatrics·2026

Development and Internal Validation of Neonatal Outcomes Prediction Score (NOPS) and Model for Neonates of 22-29 weeks' Gestation on Postnatal days 7, 14, and 28.

The Journal of pediatrics·2026

Feasibility of Surfactant Delivery via Preterm Supraglottic Airways in Infants with Birth Weights of 800-1500 g.

The Journal of pediatrics·2026

Feedback with Education versus Digital Ototscopy for Acute Otitis Media Diagnosis and Treatment.

The Journal of pediatrics·2026

Newborn screening and biobanking for preventable genetic disorders in Mongolia: A developing country perspective.

Regenerative therapy·2026

Whole-genome resequencing with multidimensional annotation revealed pathogenic networks in sirenomelia.

Italian journal of pediatrics·2026

Human Loss-of-Function ZNRF3 Mutation Impairs Adipose Thermogenesis and Drives Subcutaneous Fat Expansion.

Diabetes·2026

Integrated genetic identification and molecular dynamics simulations in a novel LOXL3 genetic mutation associated with Stickler syndrome.

Frontiers in genetics·2026

The ZBTB16/CUL3/ROC1 ubiquitin ligase drives the degradation of pathogenic pendrin (SLC26A4) protein variants.

Journal of biomedical science·2026

Identification and functional characterization of a SUZ12 frameshift variant in a Chinese family with Imagawa-Matsumoto syndrome.

BMC medical genomics·2026

Related Experiment Videos

Clinical genetics conference: progress in understanding muscle disease

Related Concept Videos

Ribosomal RNA gene sequences and hominoid phylogeny.

Sequence and structure correlation of human ribosomal transcribed spacers.

Human ribosomal DNA: novel sequence organization in a 4.5-kb region upstream from the promoter.

The role of cytologic NOR variants in the etiology of trisomy 21.

Human 28S ribosomal RNA sequence heterogeneity.

ASHG activities relative to education: Human genetics as a component of medical school curricula: A report to the American society of human genetics.

Does Timing Matter? A Clinical Trial of Supporting Play Exploration and Early Development Intervention (SPEEDI) for Infants Born Preterm in the First Months of Life.

Housing Insecurity Among Children of Incarcerated Parents in the United States.

Meningococcal B Vaccination Patterns Across 10 Integrated Health Systems within Vaccine Safety Datalink, 2015-2023.

Development and Internal Validation of Neonatal Outcomes Prediction Score (NOPS) and Model for Neonates of 22-29 weeks' Gestation on Postnatal days 7, 14, and 28.

Feasibility of Surfactant Delivery via Preterm Supraglottic Airways in Infants with Birth Weights of 800-1500 g.

Feedback with Education versus Digital Ototscopy for Acute Otitis Media Diagnosis and Treatment.

Newborn screening and biobanking for preventable genetic disorders in Mongolia: A developing country perspective.

Whole-genome resequencing with multidimensional annotation revealed pathogenic networks in sirenomelia.

Human Loss-of-Function ZNRF3 Mutation Impairs Adipose Thermogenesis and Drives Subcutaneous Fat Expansion.

Integrated genetic identification and molecular dynamics simulations in a novel LOXL3 genetic mutation associated with Stickler syndrome.

The ZBTB16/CUL3/ROC1 ubiquitin ligase drives the degradation of pathogenic pendrin (SLC26A4) protein variants.

Identification and functional characterization of a SUZ12 frameshift variant in a Chinese family with Imagawa-Matsumoto syndrome.

Related Experiment Videos

Clinical genetics conference: progress in understanding muscle disease

Related Concept Videos

Related Articles