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Genetic and developmental basis of renal coloboma (papillorenal) syndrome
Lisa A. Schimmenti
Pediatric Genetics & Metabolism
Research output
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Contribution to journal
›
Article
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peer-review
6
Scopus citations
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Dive into the research topics of 'Genetic and developmental basis of renal coloboma (papillorenal) syndrome'. Together they form a unique fingerprint.
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Keyphrases
Coloboma
100%
PAX2
100%
Papillorenal Syndrome
100%
Visual Acuity
50%
Kidney
50%
Zebrafish
50%
End-stage Renal Disease
50%
Cyst
50%
Ophthalmic Findings
50%
Optic Nerve
50%
Renal Coloboma Syndrome
50%
Optic Disc
50%
Paired Box Gene
50%
Retinal Blood Vessels
50%
Retinal Vasculature
50%
Optic Nerve Hypoplasia
50%
Pax2a
50%
Microphthalmia
50%
Severe Impairment
50%
Posterior Staphyloma
50%
Optic Nerve pit
50%
Phenotypic Observation
50%
Optic Nerve Disorders
50%
Patient's Will
50%
Autosomal Dominant mutation
50%
Biochemistry, Genetics and Molecular Biology
Genetics
100%
Vascularization
100%
Visual Acuity
100%
Zebra Fish
100%
Autosomal Dominant Inheritance
100%
Paired Box Transcription Factor
100%
Transcription Factor PAX2
100%
Medicine and Dentistry
Optic Nerve
100%
Coloboma
100%
Vascularity
33%
Retinal Blood Vessel
33%
End Stage Renal Disease
33%
Visual Acuity
33%
Autosomal Dominant Inheritance
33%
Optic Disc
33%
Optic Nerve Hypoplasia
33%
Microphthalmia
33%
Transcription Factor PAX2
33%
Nerve Malformation
33%
Staphyloma
33%
Paired Box Transcription Factor
33%