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Melinda Procter

Showing results (11-20 of 18) with videos related to

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Journal of Clinical Pathology|October 2, 2007
Genotypes and serum concentrations of human alpha-1-antitrypsin "P" protein variants in a clinical populationJoshua A Bornhorst, Fernanda R O Calderon, Melinda Procter, et al.
American Journal of Clinical Pathology|April 10, 2014
Challenging identification of a novel PiISF and the rare PiMmaltonZ α1-antitrypsin deficiency variants in two patientsBrenda B Suh-Lailam, Melinda Procter, Patti Krautscheid, et al.
Molecular Genetics & Genomic Medicine|August 5, 2022
Atypical presentation of Angelman syndrome with intact expressive language due to low-level mosaicismRuchi Punatar, Alena Egense, Rong Mao, et al.
Frontiers in Neurology|November 16, 2020
Severe Distal Motor Involvement in a Non-compliant Adult With Biotinidase Deficiency: The Necessity of Life-Long Biotin TherapyGéraldine Van Winckel, Diana Ballhausen, Barry Wolf, et al.
American Journal of Medical Genetics. Part A|July 16, 2008
Homozygous deletions of a copy number change detected by array CGH: a new cause for mental retardation?Cynthia J Curry, Rong Mao, Emily Aston, et al.
Genetic Testing and Molecular Biomarkers|June 22, 2011
Verification of multiplex ligation-dependent probe amplification probes in the absence of positive samplesWhitney Wooderchak-Donahue, Cecily Vaughn, Lan-Szu Chou, et al.
Nature Communications|September 22, 2015
Impaired PIEZO1 function in patients with a novel autosomal recessive congenital lymphatic dysplasiaViktor Lukacs, Jayanti Mathur, Rong Mao, et al.
The Journal of Molecular Diagnostics : JMD|July 15, 2014
Noncontinuously binding loop-out primers for avoiding problematic DNA sequences in PCR and sanger sequencingKelli Sumner, Jeffrey J Swensen, Melinda Procter, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Journal of Clinical Pathology|October 2, 2007
Genotypes and serum concentrations of human alpha-1-antitrypsin "P" protein variants in a clinical populationJoshua A Bornhorst, Fernanda R O Calderon, Melinda Procter, et al.
American Journal of Clinical Pathology|April 10, 2014
Challenging identification of a novel PiISF and the rare PiMmaltonZ α1-antitrypsin deficiency variants in two patientsBrenda B Suh-Lailam, Melinda Procter, Patti Krautscheid, et al.
Molecular Genetics & Genomic Medicine|August 5, 2022
Atypical presentation of Angelman syndrome with intact expressive language due to low-level mosaicismRuchi Punatar, Alena Egense, Rong Mao, et al.
Frontiers in Neurology|November 16, 2020
Severe Distal Motor Involvement in a Non-compliant Adult With Biotinidase Deficiency: The Necessity of Life-Long Biotin TherapyGéraldine Van Winckel, Diana Ballhausen, Barry Wolf, et al.
American Journal of Medical Genetics. Part A|July 16, 2008
Homozygous deletions of a copy number change detected by array CGH: a new cause for mental retardation?Cynthia J Curry, Rong Mao, Emily Aston, et al.
Genetic Testing and Molecular Biomarkers|June 22, 2011
Verification of multiplex ligation-dependent probe amplification probes in the absence of positive samplesWhitney Wooderchak-Donahue, Cecily Vaughn, Lan-Szu Chou, et al.
Nature Communications|September 22, 2015
Impaired PIEZO1 function in patients with a novel autosomal recessive congenital lymphatic dysplasiaViktor Lukacs, Jayanti Mathur, Rong Mao, et al.
The Journal of Molecular Diagnostics : JMD|July 15, 2014
Noncontinuously binding loop-out primers for avoiding problematic DNA sequences in PCR and sanger sequencingKelli Sumner, Jeffrey J Swensen, Melinda Procter, et al.
Pageof 2