Virginia V. Michels

Medical Genetics
200 1st St Sw
Rochester, MN 55905

Last Updated: 09/26/2026

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Found 4 publications

TNNI3K mutation in familial syndrome of conduction system disease, atrial tachyarrhythmia and dilated cardiomyopathy.

TNNI3K mutation in familial syndrome of conduction system disease, atrial tachyarrhythmia and dilated cardiomyopathy.

Journal: Human molecular genetics
Published: June 14, 2014

Similarity of geleophysic dysplasia and Weill-Marchesani syndrome.

Similarity of geleophysic dysplasia and Weill-Marchesani syndrome.

Journal: American journal of medical genetics. Part A
Published: March 29, 2013

Aripiprazole and trazodone cause elevations of 7-dehydrocholesterol in the absence of Smith-Lemli-Opitz Syndrome.

Aripiprazole and trazodone cause elevations of 7-dehydrocholesterol in the absence of Smith-Lemli-Opitz Syndrome.

Journal: Molecular genetics and metabolism
Published: February 25, 2013

Homozygosity mapping and exome sequencing reveal GATAD1 mutation in autosomal recessive dilated cardiomyopathy.

Homozygosity mapping and exome sequencing reveal GATAD1 mutation in autosomal recessive dilated cardiomyopathy.

Journal: Circulation. Cardiovascular genetics
Published: October 04, 2011
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Last Updated: 09/26/2026