Popliteal pterygium syndrome in monozygous twins

Segregation of enlarged vestibular aqueducts in families with non-diagnostic SLC26A4 genotypes.

Journal of medical genetics·2009

Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontia.

Clinical genetics·2008

Multiclonal outbreak of methicillin-resistant Staphylococcus aureus infections on a collegiate football team.

Epidemiology and infection·2008

Haplogroup analysis supports a pathogenic role for the 7510T>C mutation of mitochondrial tRNA(Ser(UCN)) in sensorineural hearing loss.

Clinical genetics·2007

A novel locus for autosomal dominant non-syndromic deafness, DFNA53, maps to chromosome 14q11.2-q12.

Journal of medical genetics·2005

Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafness.

Journal of medical genetics·2003

Limb anomalies from evolutionary, developmental, and genetic perspectives.

Birth defects original article series·1996

Multisite neural tube closure in humans.

Birth defects original article series·1996

Teprotumumab Effects on Thyroid Eye Disease in a Japanese MRI Study: Comparison with Intravenous Glucocorticoid Therapy.

The Journal of clinical endocrinology and metabolism·2026

Research progress in the clinical application of AI in strabismus.

Strabismus·2026

Distance-dependent changes in deviation control after alternate occlusion therapy in children with intermittent exotropia: a retrospective pilot study.

Strabismus·2026

Assessment of the Optic Nerve Sheath Diameter by Bedside Sonography and Its Correlation With the Glasgow Coma Score in the Outcome of Patients With Sepsis-Associated Encephalopathy.

Cureus·2026

Enzymatic glycosylation as a potential molecular link between Alzheimer's disease and glaucoma.

International journal of ophthalmology·2026

Diagnostic value of urinary albumin creatinine ratio in predicting vision-threatening diabetic retinopathy in patients with diabetes: a systematic review and Meta-analysis.

International journal of ophthalmology·2026

Related Experiment Videos

Popliteal pterygium syndrome in monozygous twins

Related Concept Videos

Segregation of enlarged vestibular aqueducts in families with non-diagnostic SLC26A4 genotypes.

Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontia.

Multiclonal outbreak of methicillin-resistant Staphylococcus aureus infections on a collegiate football team.

Haplogroup analysis supports a pathogenic role for the 7510T>C mutation of mitochondrial tRNA(Ser(UCN)) in sensorineural hearing loss.

A novel locus for autosomal dominant non-syndromic deafness, DFNA53, maps to chromosome 14q11.2-q12.

Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafness.

Limb anomalies from evolutionary, developmental, and genetic perspectives.

Multisite neural tube closure in humans.

Teprotumumab Effects on Thyroid Eye Disease in a Japanese MRI Study: Comparison with Intravenous Glucocorticoid Therapy.

Research progress in the clinical application of AI in strabismus.

Distance-dependent changes in deviation control after alternate occlusion therapy in children with intermittent exotropia: a retrospective pilot study.

Assessment of the Optic Nerve Sheath Diameter by Bedside Sonography and Its Correlation With the Glasgow Coma Score in the Outcome of Patients With Sepsis-Associated Encephalopathy.

Enzymatic glycosylation as a potential molecular link between Alzheimer's disease and glaucoma.

Diagnostic value of urinary albumin creatinine ratio in predicting vision-threatening diabetic retinopathy in patients with diabetes: a systematic review and Meta-analysis.

Related Experiment Videos

Popliteal pterygium syndrome in monozygous twins

Related Concept Videos

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