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

Early visual response provides additional prognostic value beyond baseline OCT features in diabetic macular edema.

European journal of ophthalmology·2026

Association of fenofibrate use with progression of ocular disease in individuals with diabetes.

The British journal of ophthalmology·2026

Aflibercept 8 mg versus faricimab for macular oedema due to retinal vein occlusion: a systematic review and network meta-analysis.

The British journal of ophthalmology·2026

Long-term complications of conjunctival tattooing: pigment aggregation and corneal dellen formation after eight years.

BMJ case reports·2026

Repeatability and Agreement between novel SS-OCT VG2 and CASIA2 in Anterior Segment Parameters.

Photodiagnosis and photodynamic therapy·2026

Effects of Different Refractive Status on Retinal and Choroidal Thickness and Blood Flow in Children Assessed by Optical Coherence Tomography Angiography.

Photodiagnosis and photodynamic therapy·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.

Early visual response provides additional prognostic value beyond baseline OCT features in diabetic macular edema.

Association of fenofibrate use with progression of ocular disease in individuals with diabetes.

Aflibercept 8 mg versus faricimab for macular oedema due to retinal vein occlusion: a systematic review and network meta-analysis.

Long-term complications of conjunctival tattooing: pigment aggregation and corneal dellen formation after eight years.

Repeatability and Agreement between novel SS-OCT VG2 and CASIA2 in Anterior Segment Parameters.

Effects of Different Refractive Status on Retinal and Choroidal Thickness and Blood Flow in Children Assessed by Optical Coherence Tomography Angiography.

Related Experiment Videos

Popliteal pterygium syndrome in monozygous twins

Related Concept Videos

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