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Virginia V Michels

Showing results (1-10 of 12) with videos related to

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Mayo Clinic Proceedings|January 26, 2005
Genetic testing: practical, ethical, and counseling considerationsRegina E Ensenauer, Virginia V Michels, Shanda S Reinke
American Journal of Medical Genetics. Part A|February 17, 2007
Delineation of the cryptic 1qter deletion phenotypeJ Lawrence Merritt, Ying Zou, Syed M Jalal, et al.
Mayo Clinic Proceedings|June 11, 2005
Usual interstitial pneumonia complicating dyskeratosis congenitaJames P Utz, Jay H Ryu, Jeffrey L Myers, et al.
Archives of Surgery (Chicago, Ill. : 1960)|June 7, 2002
Pheochromocytomas and paragangliomas in von Hippel-Lindau disease: a role for laparoscopic and cortical-sparing surgeryMercedeh Baghai, Geoffrey B Thompson, William F Young, et al.
Journal of the American College of Cardiology|February 15, 2005
Prevalence and clinical manifestations of 22q11.2 microdeletion in adults with selected conotruncal anomaliesLuc M Beauchesne, Carole A Warnes, Heidi M Connolly, et al.
Journal of the American College of Cardiology|August 29, 2009
Mutations in ribonucleic acid binding protein gene cause familial dilated cardiomyopathyKatharine M Brauch, Margaret L Karst, Kathleen J Herron, et al.
JAMA|January 27, 2005
Sodium channel mutations and susceptibility to heart failure and atrial fibrillationTimothy M Olson, Virginia V Michels, Jeffrey D Ballew, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 25, 2003
Utility of subtelomeric fluorescent DNA probes for detection of chromosome anomalies in 425 patientsSyed M Jalal, Aaron R Harwood, Gurbax S Sekhon, et al.
Circulation. Cardiovascular Genetics|October 4, 2011
Homozygosity mapping and exome sequencing reveal GATAD1 mutation in autosomal recessive dilated cardiomyopathyJeanne L Theis, Katharine M Sharpe, Martha E Matsumoto, et al.
American Journal of Medical Genetics. Part A|July 13, 2006
Mosaic ring 20 with no detectable deletion by FISH analysis: Characteristic seizure disorder and literature reviewYing S Zou, Daniel L Van Dyke, Erik C Thorland, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Mayo Clinic Proceedings|January 26, 2005
Genetic testing: practical, ethical, and counseling considerationsRegina E Ensenauer, Virginia V Michels, Shanda S Reinke
American Journal of Medical Genetics. Part A|February 17, 2007
Delineation of the cryptic 1qter deletion phenotypeJ Lawrence Merritt, Ying Zou, Syed M Jalal, et al.
Mayo Clinic Proceedings|June 11, 2005
Usual interstitial pneumonia complicating dyskeratosis congenitaJames P Utz, Jay H Ryu, Jeffrey L Myers, et al.
Archives of Surgery (Chicago, Ill. : 1960)|June 7, 2002
Pheochromocytomas and paragangliomas in von Hippel-Lindau disease: a role for laparoscopic and cortical-sparing surgeryMercedeh Baghai, Geoffrey B Thompson, William F Young, et al.
Journal of the American College of Cardiology|February 15, 2005
Prevalence and clinical manifestations of 22q11.2 microdeletion in adults with selected conotruncal anomaliesLuc M Beauchesne, Carole A Warnes, Heidi M Connolly, et al.
Journal of the American College of Cardiology|August 29, 2009
Mutations in ribonucleic acid binding protein gene cause familial dilated cardiomyopathyKatharine M Brauch, Margaret L Karst, Kathleen J Herron, et al.
JAMA|January 27, 2005
Sodium channel mutations and susceptibility to heart failure and atrial fibrillationTimothy M Olson, Virginia V Michels, Jeffrey D Ballew, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 25, 2003
Utility of subtelomeric fluorescent DNA probes for detection of chromosome anomalies in 425 patientsSyed M Jalal, Aaron R Harwood, Gurbax S Sekhon, et al.
Circulation. Cardiovascular Genetics|October 4, 2011
Homozygosity mapping and exome sequencing reveal GATAD1 mutation in autosomal recessive dilated cardiomyopathyJeanne L Theis, Katharine M Sharpe, Martha E Matsumoto, et al.
American Journal of Medical Genetics. Part A|July 13, 2006
Mosaic ring 20 with no detectable deletion by FISH analysis: Characteristic seizure disorder and literature reviewYing S Zou, Daniel L Van Dyke, Erik C Thorland, et al.
Pageof 2