58 Publications (Page 2 of 3)
2016
The Spectrum of Clinical Utilities in Molecular Pathology Testing Procedures for Inherited Conditions and Cancer: A Report of the Association for Molecular PathologyJoseph, Loren⋅Joseph, Loren⋅Cankovic, Milena⋅Cankovic, Milena⋅Caughron, Samuel⋅Caughron, Samuel⋅Chandra, Pranil⋅Chandra, Pranil⋅Emmadi, Rajyasree⋅Emmadi, Rajyasree⋅Hagenkord, Jill⋅Hagenkord, Jill⋅Hallam, Stephanie⋅Hallam, Stephanie⋅Jewell, Kay E⋅Jewell, Kay E⋅Klein, Roger D⋅Klein, Roger D⋅Pratt, Victoria M⋅Pratt, Victoria M⋅Rothberg, Paul G⋅Rothberg, Paul G⋅Temple-Smolkin, Robyn L⋅Temple-Smolkin, Robyn L⋅Lyon, Elaine and Lyon, ElaineThe Journal of molecular diagnostics : JMD, vol. 18, (no. 5), pp. 619, 2016-09-00.
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2015
Analytic Validity of Genomic TestingPratt, Victoria M and Leonard, Debra G. BNAM Perspectives, vol. 5, (no. 1), 2015-01-15.
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FDA's draft guidance on laboratory‐developed tests increases clinical and economic risk to adoption of pharmacogenetic testingLevy, Kenneth D⋅Levy, Kenneth D⋅Pratt, Victoria M⋅Pratt, Victoria M⋅Skaar, Todd C⋅Skaar, Todd C⋅Vance, Gail H⋅Vance, Gail H⋅Flockhart, David A and Flockhart, David AThe Journal of Clinical Pharmacology, vol. 55, (no. 7), pp. 727, July 2015.
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Report of new haplotype for ABCC2 gene: rs17222723 and rs8187718 in cis.Pratt, Victoria M⋅Beyer, Brittany N⋅Koller, Daniel L⋅Skaar, Todd C⋅Flockhart, David A⋅Levy, Kenneth D and Vance, Gail HThe Journal of molecular diagnostics : JMD, vol. 17, (no. 2), pp. 201-205, March 2015.
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2014
Revisiting oversight and regulation of molecular-based laboratory-developed tests: a position statement of the Association for Molecular PathologyFerreira-Gonzalez, Andrea⋅Ferreira-Gonzalez, Andrea⋅Emmadi, Rajyasree⋅Emmadi, Rajyasree⋅Day, Stephen P⋅Day, Stephen P⋅Klees, Robert F⋅Klees, Robert F⋅Leib, Jennifer R⋅Leib, Jennifer R⋅Lyon, Elaine⋅Lyon, Elaine⋅Nowak, Jan A⋅Nowak, Jan A⋅Pratt, Victoria M⋅Pratt, Victoria M⋅Williams, Mary S⋅Williams, Mary S⋅Klein, Roger D and Klein, Roger DThe Journal of molecular diagnostics : JMD, vol. 16, (no. 1), pp. 6, 2014-Jan.
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2013
Mosaic isochromosome 15q and maternal uniparental isodisomy for chromosome 15 in a patient with morbid obesity and variant PWS‐like phenotypeWang, Jia‐Chi⋅Vaccarello‐Cruz, Mary⋅Ross, Leslie⋅Owen, Renius⋅Pratt, Victoria M⋅Lightman, Katherine⋅Liu, Yan⋅Hafezi, Katayoun⋅Cherif, Dhia and Sahoo, TrilochanAmerican Journal of Medical Genetics Part A, vol. 161, (no. 7), pp. 1701, July 2013.
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2012
Laboratory testing of CYP2D6 alleles in relation to tamoxifen therapy.Lyon, E.⋅Lyon, Elaine⋅Gastier Foster, J.⋅Gastier Foster, Julie M⋅Gastier Foster, Julie⋅Palomaki, Glenn E⋅Palomaki, G.E.⋅Pratt, V.M.⋅Pratt, Victoria M⋅Reynolds, Kristen⋅Reynolds, K.⋅Fernanda Sábato, M.⋅Sábato, M F⋅Scott, Stuart⋅Scott, S.A.⋅Vitazka, P. and Vitazka, PatrikGenetics in medicine : official journal of the American College of Medical Genetics, vol. 14, (no. 12), pp. 990-1000, 2012/Dec.
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Opportunities and challenges associated with clinical diagnostic genome sequencing: a report of the Association for Molecular PathologySchrijver, Iris⋅Schrijver, Iris⋅Schrijver, Iris⋅Schrijver, Iris⋅Aziz, Nazneen⋅Aziz, Nazneen⋅Aziz, Nazneen⋅Aziz, Nazneen⋅Farkas, Daniel H⋅Farkas, Daniel H⋅Farkas, Daniel H⋅Farkas, Daniel H⋅Furtado, Manohar⋅Furtado, Manohar⋅Furtado, Manohar⋅Furtado, Manohar⋅Ferreira Gonzalez, Andrea⋅Gonzalez, Andrea Ferreira⋅Gonzalez, Andrea Ferreira⋅Gonzalez, Andrea Ferreira⋅Greiner, Timothy C⋅Greiner, Timothy C⋅Greiner, Timothy C⋅Greiner, Timothy C⋅Grody, Wayne W⋅Grody, Wayne W⋅Grody, Wayne W⋅Grody, Wayne W⋅Hambuch, Tina⋅Hambuch, Tina⋅Hambuch, Tina⋅Hambuch, Tina⋅Kalman, Lisa⋅Kalman, Lisa⋅Kalman, Lisa⋅Kalman, Lisa⋅Kant, Jeffrey A⋅Kant, Jeffrey A⋅Kant, Jeffrey A⋅Kant, Jeffrey A⋅Klein, Roger D⋅Klein, Roger D⋅Klein, Roger D⋅Klein, Roger D⋅Leonard, Debra G B⋅Leonard, Debra G⋅Leonard, Debra G B⋅Leonard, Debra G B⋅Lubin, Ira M⋅Lubin, Ira M⋅Lubin, Ira M⋅Lubin, Ira M⋅Mao, Rong⋅Mao, Rong⋅Mao, Rong⋅Mao, Rong⋅Nagan, Narasimhan⋅Nagan, Narasimhan⋅Nagan, Narasimhan⋅Nagan, Narasimhan⋅Pratt, Victoria M⋅Pratt, Victoria M⋅Pratt, Victoria M⋅Pratt, Victoria M⋅Sobel, Mark E⋅Sobel, Mark E⋅Sobel, Mark E⋅Sobel, Mark E⋅Voelkerding, Karl V⋅Voelkerding, Karl V⋅Voelkerding, Karl V⋅Voelkerding, Karl V⋅Gibson, Jane S⋅Gibson, Jane S⋅Gibson, Jane S and Gibson, Jane SThe Journal of molecular diagnostics : JMD, vol. 14, (no. 6), pp. 540, 2012-Nov.
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2011
Cystic fibrosis testing 8 years on: Lessons learned from carrier screening and sequencing analysisStrom, Charles M⋅Crossley, Beryl⋅Buller-Buerkle, Arlene⋅Jarvis, Michael⋅Quan, Franklin⋅Peng, Mei⋅Muralidharan, Kasinathan⋅Pratt, Victoria⋅Redman, Joy B and Sun, WeiminGenetics in medicine : official journal of the American College of Medical Genetics, vol. 13, (no. 2), pp. 172, 2011-Feb.
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2010
A standardized framework for the validation and verification of clinical molecular genetic testsMattocks, Christopher⋅Morris, Michael⋅Matthijs, Gert⋅Swinnen, Elfriede⋅Corveleyn, Anniek⋅Dequeker, Elisabeth⋅Müller, Clemens⋅Pratt, Victoria and Wallace, Andrew2010-12.
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Characterization of 107 genomic DNA reference materials for CYP2D6, CYP2C19, CYP2C9, VKORC1, and UGT1A1: a GeT-RM and Association for Molecular Pathology collaborative project.Pratt, Victoria M⋅Zehnbauer, Barbara⋅Wilson, Jean A⋅Baak, Ruth⋅Babic, Nikolina⋅Bettinotti, Maria⋅Buller, Arlene⋅Butz, Ken⋅Campbell, Matthew⋅Civalier, Chris⋅El-Badry, Abdalla⋅Farkas, Daniel H⋅Lyon, Elaine⋅Mandal, Saptarshi⋅McKinney, Jason⋅Muralidharan, Kasinathan⋅Noll, LeAnne⋅Sander, Tara⋅Shabbeer, Junaid⋅Smith, Chingying⋅Telatar, Milhan⋅Toji, Lorraine⋅Vairavan, Anand⋅Vance, Carlos⋅Weck, Karen E⋅Wu, Alan H⋅Yeo, Kiang-Teck J⋅Zeller, Markus and Kalman, LisaThe Journal of molecular diagnostics : JMD, vol. 12, (no. 6), pp. 835-46, 2010/Nov.
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Identification of Novel CYP2D7-2D6 Hybrids: Non-Functional and Functional Variants.Gaedigk, Andrea⋅Jaime, Lazara K⋅Bertino, Joseph S⋅Berard, Anick⋅Pratt, Victoria M⋅Bradfordand, L D and Leeder, J SFrontiers in pharmacology, vol. 1, pp. 121, 2010.
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2009
Clinician Perspectives about Molecular Genetic Testing for Heritable Conditions and Development of a Clinician-Friendly Laboratory ReportLubin, Ira M⋅Lubin, Ira⋅McGovern, Margaret⋅McGovern, Margaret M⋅Gibson, Zoe⋅Gibson, Zoe⋅Gross, Susan J⋅Gross, Susan⋅Lyon, Elaine⋅Lyon, Elaine⋅Pagon, Roberta A⋅Pagon, Roberta⋅Pratt, Victoria⋅Pratt, Victoria M⋅Rashid, Jamila⋅Rashid, Jamila⋅Shaw, Colleen⋅Shaw, Colleen⋅Stoddard, Lander⋅Stoddard, Lander⋅Trotter, Tracy L⋅Trotter, Tracy⋅Williams, Marc⋅Williams, Marc S⋅Amos Wilson, Jean⋅Amos Wilson, Jean⋅Pass, Kenneth and Pass, KennethJournal of Molecular Diagnostics, The, vol. 11, (no. 2), pp. 171, 2009.
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CpG Methylation Analysis--Current Status of Clinical Assays and Potential Applications in Molecular Diagnostics: A Report of the Association for Molecular PathologySepulveda, Antonia R⋅Sepulveda, Antonia⋅Sepulveda, Antonia⋅Jones, Dan⋅Jones, Dan⋅Jones, Dan⋅Ogino, Shuji⋅Ogino, Shuji⋅Ogino, Shuji⋅Samowitz, Wade⋅Samowitz, Wade⋅Samowitz, Wade⋅Gulley, Margaret⋅Gulley, Margaret L⋅Gulley, Margaret⋅Edwards, Robin⋅Edwards, Robin⋅Edwards, Robin⋅Levenson, Victor⋅Levenson, Victor⋅Levenson, Victor⋅Pratt, Victoria⋅Pratt, Victoria M⋅Pratt, Victoria⋅Yang, Bin⋅Yang, Bin⋅Yang, Bin⋅Nafa, Khedoudja⋅Nafa, Khedoudja⋅Nafa, Khedoudja⋅Yan, Liying⋅Yan, Liying⋅Yan, Liying⋅Vitazka, Patrick⋅Vitazka, Patrick and Vitazka, PatrickJournal of Molecular Diagnostics, vol. 11, (no. 4), pp. 278, 20090701.
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Development and Characterization of Reference Materials for MTHFR , SERPINA1 , RET , BRCA1 , and BRCA2 Genetic TestingBarker, Shannon⋅Barker, Shannon⋅Bale, Sherri⋅Bale, Sherri⋅Booker, Jessica⋅Booker, Jessica⋅Buller, Arlene⋅Buller, Arlene⋅Das, Soma⋅Das, Soma⋅Friedman, Kenneth⋅Friedman, Kenneth J⋅Godwin, Andrew⋅Godwin, Andrew⋅Grody, Wayne W⋅Grody, Wayne⋅Highsmith, Edward⋅Highsmith, Edward⋅Kant, Jeffery A⋅Kant, Jeffery⋅Lyon, Elaine⋅Lyon, Elaine⋅Mao, Rong⋅Mao, Rong⋅Monaghan, Kristin⋅Monaghan, Kristin G⋅Payne, Deborah⋅Payne, Deborah A⋅Pratt, Victoria M⋅Pratt, Victoria⋅Schrijver, Iris⋅Schrijver, Iris⋅Shrimpton, Antony⋅Shrimpton, Antony E⋅Spector, Elaine⋅Spector, Elaine⋅Telatar, Milhan⋅Telatar, Milhan⋅Toji, Lorraine⋅Toji, Lorraine⋅Weck, Karen⋅Weck, Karen⋅Zehnbauer, Barbara⋅Zehnbauer, Barbara⋅Kalman, Lisa and Kalman, Lisa VJournal of Molecular Diagnostics, The, vol. 11, (no. 6), pp. 561, 2009.
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Development of Genomic Reference Materials for Cystic Fibrosis Genetic TestingPratt, Victoria M⋅Pratt, Victoria⋅Caggana, Michele⋅Caggana, Michele⋅Bridges, Christina⋅Bridges, Christina⋅Buller, Arlene M⋅Buller, Arlene⋅DiAntonio, Lisa⋅DiAntonio, Lisa⋅Highsmith, W.⋅Highsmith, W. E⋅Holtegaard, Leonard M⋅Holtegaard, Leonard⋅Muralidharan, Kasinathan⋅Muralidharan, Kasinathan⋅Rohlfs, Elizabeth M⋅Rohlfs, Elizabeth⋅Tarleton, Jack⋅Tarleton, Jack⋅Toji, Lorraine⋅Toji, Lorraine⋅Barker, Shannon D⋅Barker, Shannon⋅Kalman, Lisa and Kalman, Lisa VJournal of Molecular Diagnostics, The, vol. 11, (no. 3), pp. 193, 2009.
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The interface of Medicare coverage decision-making and emerging molecular-based laboratory testingBurken, Mitchell I⋅Burken, Mitchell I⋅Wilson, Kathleen S⋅Wilson, Kathleen S⋅Heller, Karen⋅Heller, Karen⋅Pratt, Victoria M⋅Pratt, Victoria M⋅Schoonmaker, Michele M⋅Schoonmaker, Michele M⋅Seifter, Eric and Seifter, EricGenetics in medicine : official journal of the American College of Medical Genetics, vol. 11, (no. 4), pp. 231, 2009-Apr.
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2008
Consensus Characterization of 16 FMR1 Reference Materials: A Consortium StudyAmos Wilson, Jean⋅Amos Wilson, Jean⋅Wilson, J.A.⋅Pratt, Victoria M⋅Pratt, Victoria⋅Pratt, V.M.⋅Phansalkar, Amit⋅Phansalkar, A.⋅Phansalkar, Amit⋅Muralidharan, K.⋅Muralidharan, Kasinathan⋅Muralidharan, Kasinathan⋅Highsmith Jr., W.E.⋅Highsmith, W. E⋅Highsmith, W.⋅Beck, Jeanne C⋅Beck, Jeanne⋅Beck, J.C.⋅Bridgeman, Scott⋅Bridgeman, Scott⋅Bridgeman, S.⋅Courtney, E.M.⋅Courtney, Ebony M⋅Courtney, Ebony⋅Epp, L.⋅Epp, Lidia⋅Epp, Lidia⋅Ferreira-Gonzalez, A.⋅Ferreira-Gonzalez, Andrea⋅Ferreira Gonzalez, Andrea⋅Hjelm, Nick L⋅Hjelm, Nick⋅Hjelm, N.L.⋅Holtegaard, Leonard M⋅Holtegaard, Leonard⋅Holtegaard, L.M.⋅Jama, Mohamed⋅Jama, Mohamed A⋅Jama, M.A.⋅Jakupciak, John P⋅Jakupciak, John⋅Jakupciak, J.P.⋅Johnson, M.A.⋅Johnson, Monique⋅Johnson, Monique A⋅Labrousse, Paul⋅Labrousse, P.⋅Labrousse, Paul⋅Lyon, E.⋅Lyon, Elaine⋅Lyon, Elaine⋅Prior, T.W.⋅Prior, Thomas⋅Prior, Thomas W⋅Richards, C.S.⋅Richards, C.⋅Richards, C S⋅Richie, Kristy L⋅Richie, K.L.⋅Richie, Kristy⋅Roa, Benjamin⋅Roa, Benjamin B⋅Roa, B.B.⋅Rohlfs, Elizabeth M⋅Rohlfs, E.M.⋅Rohlfs, Elizabeth⋅Sellers, Tina⋅Sellers, Tina⋅Sellers, T.⋅Sherman, Stephanie⋅Sherman, Stephanie L⋅Sherman, S.L.⋅Siegrist, Karen⋅Siegrist, Karen A⋅Siegrist, K.A.⋅Silverman, Lawrence⋅Silverman, Lawrence M⋅Silverman, L.M.⋅Wiszniewska, Joanna⋅Wiszniewska, Joanna⋅Wiszniewska, J.⋅Kalman, Lisa⋅Kalman, L.V.⋅Kalman, Lisa V⋅Bossler, A.⋅Dillon, D.⋅Dolan, M.⋅Gastier-Foster, J.⋅Jones, D.⋅Sepulveda, A.⋅Stellrecht, K. and Wolff, D.A.Journal of Molecular Diagnostics, The, vol. 10, (no. 1), pp. 12, 2008.
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2007
Development of a Web-Based Query Tool for Quality Assurance of Clinical Molecular Genetic Test ResultsMcGinniss, Matthew⋅Chen, Rebecca⋅Pratt, Victoria⋅Buller, Arlene⋅Quan, Franklin⋅Strom, Charles⋅Sun, Weimin and Crossley, BerylJournal of Molecular Diagnostics, The, vol. 9, (no. 1), pp. 98, 2007.
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2005
Detection of 677CT/1298AC “double variant” chromosomes: Implications for interpretation of MTHFR genotyping resultsBrown, Nicholas M⋅Pratt, Victoria M⋅Buller, Arlene⋅Pike-Buchanan, Lisa⋅Redman, Joy B⋅Sun, Weimin⋅Chen, Rebecca⋅Crossley, Beryl⋅McGinniss, Matthew J⋅Quan, Franklin and Strom, Charles MGenetics in medicine : official journal of the American College of Medical Genetics, vol. 7, (no. 4), pp. 282, 2005-Apr.
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Developing a Sustainable Process to Provide Quality Control Materials for Genetic TestingChen, Bin⋅Chen, Bin⋅O' Connell, Catherine D⋅O' Connell, Catherine D⋅Boone, D Joe⋅Boone, D J⋅Amos, Jean A⋅Amos, Jean A⋅Beck, Jeanne C⋅Beck, Jeanne C⋅Chan, Maria M⋅Chan, Maria M⋅Farkas, Daniel H⋅Farkas, Daniel H⋅Lebo, Roger V⋅Lebo, Roger V⋅Richards, Carolyn Sue⋅Richards, C. S⋅Roa, Benjamin B⋅Roa, Benjamin B⋅Silverman, Lawrence M⋅Silverman, Lawrence M⋅Barton, David⋅Barton, David E⋅Bejjani, Bassem A⋅Bejjani, Bassem A⋅Belloni, Dorothy R⋅Belloni, Dorothy R⋅Bernacki, Susan H⋅Bernacki, Susan⋅Caggana, Michele⋅Caggana, Michele⋅Charache, Patricia⋅Charache, Patricia⋅Dequeker, Elisabeth⋅Dequeker, Elisabeth⋅Ferreira-Gonzalez, Andrea⋅Ferreira Gonzalez, Andrea⋅Friedman, Kenneth J⋅Friedman, Kenneth J⋅Greene, Carol L⋅Greene, Carol L⋅Grody, Wayne W⋅Grody, Wayne W⋅Highsmith, Jr, William Edward⋅Highsmith, William E⋅Hinkel, Cecelia S⋅Hinkel, Cecelia S⋅Kalman, Lisa V⋅Kalman, Lisa V⋅Lubin, Ira M⋅Lubin, Ira M⋅Lyon, Elaine⋅Lyon, Elaine⋅Payne, Deborah A⋅Payne, Deborah A⋅Pratt, Victoria M⋅Pratt, Victoria M⋅Rohlfs, Elizabeth⋅Rohlfs, Elizabeth⋅Rundell, Clark A⋅Rundell, Clark A⋅Schneider, Erasmus⋅Schneider, Erasmus⋅Willey, Ann M⋅Willey, Ann M⋅Williams, Laurina O⋅Williams, Laurina O⋅Willey, James C⋅Willey, James⋅Winn-Deen, Emily S⋅Winn-Deen, Emily S⋅Wolff, Daynna J and Wolff, Daynna JGenetics in medicine : official journal of the American College of Medical Genetics, vol. 7, (no. 8), pp. 549, 2005-Oct.
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Genetically Characterized Positive Control Cell Lines Derived from Residual Clinical Blood SamplesBernacki, Susan⋅Bernacki, Susan⋅Beck, Jeanne⋅Beck, Jeanne C⋅Stankovic, Ana K⋅Stankovic, Ana⋅Williams, Laurina⋅Williams, Laurina O⋅Amos, Jean⋅Amos, Jean⋅Snow-Bailey, Karen⋅Snow-Bailey, Karen⋅Farkas, Daniel H⋅Farkas, Daniel⋅Friez, Michael J⋅Friez, Michael⋅Hantash, Feras⋅Hantash, Feras M⋅Matteson, Karla J⋅Matteson, Karla⋅Monaghan, Kristin⋅Monaghan, Kristin G⋅Muralidharan, Kasinathan⋅Muralidharan, Kasinathan⋅Pratt, Victoria M⋅Pratt, Victoria⋅Prior, Thomas⋅Prior, Thomas W⋅Richie, Kristy⋅Richie, Kristy L⋅Levin, Barbara⋅Levin, Barbara C⋅Rohlfs, Elizabeth⋅Rohlfs, Elizabeth M⋅Schaefer, Frederick V⋅Schaefer, Frederick⋅Shrimpton, Antony E⋅Shrimpton, Antony⋅Spector, Elaine B⋅Spector, Elaine⋅Stolle, Catherine⋅Stolle, Catherine A⋅Strom, Charles M⋅Strom, Charles⋅Thibodeau, Stephen N⋅Thibodeau, Stephen⋅Cole, Eugene⋅Cole, Eugene C⋅Goodman, Barbara K⋅Goodman, Barbara⋅Stenzel, Timothy and Stenzel, Timothy TClinical Chemistry, vol. 51, (no. 11), pp. 2024, 20051101.
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2004
Cystic fibrosis population carrier screening: 2004 revision of American College of Medical Genetics mutation panelWatson, Michael S⋅Watson, Michael S⋅Cutting, Garry R⋅Cutting, Garry R⋅Desnick, Robert J⋅Desnick, Robert J⋅Driscoll, Deborah A⋅Driscoll, Deborah A⋅Klinger, Katherine⋅Klinger, Katherine⋅Mennuti, Michael⋅Mennuti, Michael⋅Palomaki, Glenn E⋅Palomaki, Glenn⋅Popovich, Bradley W⋅Popovich, Bradley W⋅Pratt, Victoria M⋅Pratt, Victoria M⋅Rohlfs, Elizabeth M⋅Rohlfs, Elizabeth M⋅Strom, Charles M⋅Strom, Charles M⋅Richards, C. S⋅Richards, C Sue⋅Witt, David R⋅Witt, David R⋅Grody, Wayne W and Grody, Wayne WGenetics in medicine : official journal of the American College of Medical Genetics, vol. 6, (no. 5), pp. 391, 2004 Sep-Oct.
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2001
Victoria PrattPratt, VictoriaFlare, vol. 23, (no. 10), pp. 188, 20011001.
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2000
Additional Copies of the Proteolipid Protein Gene Causing Pelizaeus-Merzbacher Disease Arise by Separate Integration into the X ChromosomeHodes, M.E⋅Hodes, Marion E⋅Woodward, Karen⋅Woodward, K⋅Spinner, Nancy B⋅Spinner, N B⋅Emanuel, B S⋅Emanuel, Beverly S⋅Enrico-Simon, A⋅Enrico-Simon, Agnes⋅Kamholz, John⋅Kamholz, J⋅Stambolian, Dwight⋅Stambolian, D⋅Zackai, Elaine H⋅Zackai, E H⋅Pratt, V M⋅Pratt, Victoria M⋅Thomas, I T⋅Thomas, I.T⋅Crandall, K⋅Crandall, Kerry⋅Dlouhy, S R⋅Dlouhy, Stephen R⋅Malcolm, Sue and Malcolm, SThe American Journal of Human Genetics, vol. 67, (no. 1), pp. 22, 2000.
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