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1Academic Journal
المؤلفون: Pavithra Amritkumar, Justin Margret Jeffrey, Jayasankaran Chandru, Paridhy Vanniya S, M. Kalaimathi, Rajagopalan Ramakrishnan, N. P. Karthikeyen, C. R. Srikumari Srisailapathy
المصدر: BMC Medical Genetics, Vol 19, Iss 1, Pp 1-24 (2018)
مصطلحات موضوعية: Assortative mating, GJB2 mutations, GJB6 mutations, DFNB1, Deafness, South India, Internal medicine, RC31-1245, Genetics, QH426-470
وصف الملف: electronic resource
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2Academic Journal
المؤلفون: Kaur, Maninder, Blair, Justin, Devkota, Batsal, Fortunato, Sierra, Clark, Dinah, Lawrence, Audrey, Kim, Jiwoo, Do, Wonwook, Semeo, Benjamin, Katz, Olivia, Mehta, Devanshi, Yamamoto, Nobuko, Schindler, Emma, Al Rawi, Zayd, Wallace, Nina, Wilde, Jonathan, McCallum, Jennifer, Liu, Jinglan, Xu, Dongbin, Jackson, Marie, Rentas, Stefan, Tayoun, Ahmad, Zhe, Zhang, Abdul-Rahman, Omar, Allen, Bill, Angula, Moris, Anyane-Yeboa, Kwame, Argente, Jesús, Arn, Pamela, Armstrong, Linlea, Basel-Salmon, Lina, Baynam, Gareth, Bird, Lynne, Bruegger, Daniel, Chng, Gaik-Siew, Chitayat, David, Clark, Robin, Cox, Gerald, Dave, Usha, DeBaere, Elfrede, Field, Michael, Graham, John, Gripp, Karen, Greenstein, Robert, Gupta, Neerja, Heidenreich, Randy, Hoffman, Jodi, Hopkin, Robert, Jones, Kenneth, Jones, Marilyn, Kariminejad, Ariana, Kogan, Jillene, Lace, Baiba, Leroy, Julian, Lynch, Sally, McDonald, Marie, Meagher, Kirsten, Mendelsohn, Nancy, Micule, Ieva, Moeschler, John, Nampoothiri, Sheela, Ohashi, Kaoru, Powell, Cynthia, Ramanathan, Subhadra, Raskin, Salmo, Roeder, Elizabeth, Rio, Marlene, Rope, Alan, Sangha, Karan, Scheuerle, Angela, Schneider, Adele, Shalev, Stavit, Siu, Victoria, Smith, Rosemarie, Stevens, Cathy, Tkemaladze, Tinatin, Toimie, John, Toriello, Helga, Turner, Anne, Wheeler, Patricia, White, Susan, Young, Terri, Loomes, Kathleen, Pipan, Mary, Harrington, Ann, Zackai, Elaine, Rajagopalan, Ramakrishnan, Conlin, Laura, Deardorff, Matthew, McEldrew, Deborah, Pie, Juan, Ramos, Feliciano, Musio, Antonio, Kline, Antonie, Izumi, Kosuke, Raible, Sarah, Krantz, Ian
المصدر: The American Journal of Medical Genetics - Part A. 191(8)
مصطلحات موضوعية: CdLS, Cornelia de Lange Syndrome, HDAC8, NIPBL, RAD21, SMC1A, SMC3, cohesin, genome, transcription, Humans, Nuclear Proteins, De Lange Syndrome, Transcription Factors, Cell Cycle Proteins, Phenotype, Mutation, Genomics, Genetic Association Studies, Transcriptional Elongation Factors, Histone Deacetylases, Repressor Proteins
وصف الملف: application/pdf
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3Academic Journal
المؤلفون: Hatsukami Thomas S, Marshall Julieann K, Ranchalis Jane E, Rajagopalan Ramakrishnan, Ronald James, Heagerty Patrick J, Jarvik Gail P
المصدر: Lipids in Health and Disease, Vol 8, Iss 1, p 52 (2009)
مصطلحات موضوعية: Nutritional diseases. Deficiency diseases, RC620-627
وصف الملف: electronic resource
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4Academic Journal
المؤلفون: Kilich, Gonench, Hassey, Kelly, Behrens, Edward M., Falk, Marni, Vanderver, Adeline, Rader, Daniel J., Cahill, Patrick J., Raper, Anna, Zhang, Zhe, Westerfer, Dawn, Jadhav, Tanaya, Conlin, Laura, Izumi, Kosuke, Rajagopalan, Ramakrishnan, Sullivan, Kathleen E.
المساهمون: Foundation for the National Institutes of Health
المصدر: npj Genomic Medicine ; volume 9, issue 1 ; ISSN 2056-7944
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5Academic Journal
المؤلفون: Bedoukian, Emma, Reichert, Sara, DeChene, Elizabeth, Heck, Alexandra, Hershey, Jennifer, McManus, Morgan, Marchese, Michelle, Mulchandani, Surabhi, Reynoso Santos, Francis Jeshira, Wild, K. Taylor, Wood, Kathleen, Conlin, Laura, Dulik, Matthew, Rajagopalan, Ramakrishnan, Spinner, Nancy, Krantz, Ian
المصدر: Genetics in Medicine Open ; volume 2, page 101431 ; ISSN 2949-7744
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6Academic Journal
المؤلفون: Jadhav, Tanaya, Zucco, Avery, Aruta, Matt, Dulik, Matthew, Conlin, Laura, Rajagopalan, Ramakrishnan, Wang, Jing
المصدر: Genetics in Medicine Open ; volume 2, page 101741 ; ISSN 2949-7744
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7Academic Journal
المؤلفون: Aruta, Matt, Knoblauch, Jard, Jadhav, Tanaya, Xiong, Emily, Xing, Yue, Conlin, Laura, Rajagopalan, Ramakrishnan
المصدر: Genetics in Medicine Open ; volume 2, page 101527 ; ISSN 2949-7744
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8Academic Journal
المؤلفون: Berauer, John‐Paul, Mezina, Anya I, Okou, David T, Sabo, Aniko, Muzny, Donna M, Gibbs, Richard A, Hegde, Madhuri R, Chopra, Pankaj, Cutler, David J, Perlmutter, David H, Bull, Laura N, Thompson, Richard J, Loomes, Kathleen M, Spinner, Nancy B, Rajagopalan, Ramakrishnan, Guthery, Stephen L, Moore, Barry, Yandell, Mark, Harpavat, Sanjiv, Magee, John C, Kamath, Binita M, Molleston, Jean P, Bezerra, Jorge A, Murray, Karen F, Alonso, Estella M, Rosenthal, Philip, Squires, Robert H, Wang, Kasper S, Finegold, Milton J, Russo, Pierre, Sherker, Averell H, Sokol, Ronald J, Karpen, Saul J, Network, for the Childhood Liver Disease Research
المصدر: Hepatology. 70(3)
مصطلحات موضوعية: Biomedical and Clinical Sciences, Clinical Sciences, Human Genome, Liver Disease, Rare Diseases, Kidney Disease, Congenital Structural Anomalies, Minority Health, Perinatal Period - Conditions Originating in Perinatal Period, Clinical Research, Polycystic Kidney Disease, Pediatric, Digestive Diseases, Chronic Liver Disease and Cirrhosis, Genetics, Health Disparities, 2.1 Biological and endogenous factors, Congenital, Oral and gastrointestinal, Abnormalities, Multiple, Biliary Atresia, Child, Databases, Factual, Female, Gene Expression Regulation, Developmental, Genetic Variation, Humans, Infant, Infant, Newborn, Male, Membrane Proteins, Polycystic Kidney Diseases, Retrospective Studies, Spleen, Syndrome, Exome Sequencing, Childhood Liver Disease Research Network, Medical Biochemistry and Metabolomics, Immunology, Gastroenterology & Hepatology, Clinical sciences
وصف الملف: application/pdf
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9Academic JournalGenome maps across 26 human populations reveal population-specific patterns of structural variation.
المؤلفون: Levy-Sakin, Michal, Pastor, Steven, Mostovoy, Yulia, Li, Le, Leung, Alden KY, McCaffrey, Jennifer, Young, Eleanor, Lam, Ernest T, Hastie, Alex R, Wong, Karen HY, Chung, Claire YL, Ma, Walfred, Sibert, Justin, Rajagopalan, Ramakrishnan, Jin, Nana, Chow, Eugene YC, Chu, Catherine, Poon, Annie, Lin, Chin, Naguib, Ahmed, Wang, Wei-Ping, Cao, Han, Chan, Ting-Fung, Yip, Kevin Y, Xiao, Ming, Kwok, Pui-Yan
المصدر: Nature communications. 10(1)
مصطلحات موضوعية: Chromosomes, Human, Y, Humans, Chromosome Mapping, Sequence Analysis, DNA, Computational Biology, Genomics, Phylogeny, Base Sequence, Gene Dosage, Mutation, Genome, Human, Algorithms, Female, Male, Genomic Structural Variation, Segmental Duplications, Genomic, Genetic Linkage, Chromosomes, Human, Y, Sequence Analysis, DNA, Genome, Segmental Duplications, Genomic
وصف الملف: application/pdf
URL الوصول: https://escholarship.org/uc/item/2h71h1dc
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10Academic Journal
المؤلفون: Kaur, Maninder, Blair, Justin, Devkota, Batsal, Fortunato, Sierra, Clark, Dinah, Lawrence, Audrey, Kim, Jiwoo, Do, Wonwook, Semeo, Benjamin, Katz, Olivia, Mehta, Devanshi, Yamamoto, Nobuko, Schindler, Emma, Al Rawi, Zayd, Wallace, Nina, Wilde, Jonathan J., McCallum, Jennifer, Liu, Jinglan, Xu, Dongbin, Jackson, Marie, Rentas, Stefan, Tayoun, Ahmad Abou, Zhe, Zhang, Abdul-Rahman, Omar, Allen, Bill, Angula, Moris A., Anyane-Yeboa, Kwame, Argente, Jesús, Arn, Pamela H., Armstrong, Linlea, Basel-Salmon, Lina, Baynam, Gareth, Bird, Lynne M., Bruegger, Daniel, Ch'ng, Gaik-Siew, Chitayat, David, Clark, Robin, Cox, Gerald F., Dave, Usha, DeBaere, Elfrede, Field, Michael, Graham Jr, John M., Gripp, Karen W., Greenstein, Robert, Gupta, Neerja, Heidenreich, Randy, Hoffman, Jodi, Hopkin, Robert J., Jones, Kenneth L., Jones, Marilyn C., Kariminejad, Ariana, Kogan, Jillene, Lace, Baiba, Leroy, Julian, Lynch, Sally Ann, McDonald, Marie, Meagher, Kirsten, Mendelsohn, Nancy, Micule, Ieva, Moeschler, John, Nampoothiri, Sheela, Ohashi, Kaoru, Powell, Cynthia M., Ramanathan, Subhadra, Raskin, Salmo, Roeder, Elizabeth, Rio, Marlene, Rope, Alan F., Sangha, Karan, Scheuerle, Angela E., Schneider, Adele, Shalev, Stavit, Siu, Victoria, Smith, Rosemarie, Stevens, Cathy, Tkemaladze, Tinatin, Toimie, John, Toriello, Helga, Turner, Anne, Wheeler, Patricia G., White, Susan M., Young, Terri, Loomes, Kathleen M., Pipan, Mary, Harrington, Ann Tokay, Zackai, Elaine, Rajagopalan, Ramakrishnan, Conlin, Laura, Deardorff, Matthew A., McEldrew, Deborah, Pie, Juan, Ramos, Feliciano, Musio, Antonio, Kline, Antonie D., Izumi, Kosuke, Raible, Sarah E., Krantz, Ian D.
وصف الملف: application/pdf
Relation: http://zaguan.unizar.es/record/127785
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11Academic Journal
المؤلفون: Luo, Minjie, Conlin, Laura K, Rajagopalan, Ramakrishnan
المصدر: Clinical Chemistry ; volume 69, issue 6, page 545-547 ; ISSN 0009-9147 1530-8561
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12Academic Journal
المؤلفون: Young, Eleanor, Pastor, Steven, Rajagopalan, Ramakrishnan, McCaffrey, Jennifer, Sibert, Justin, Mak, Angel CY, Kwok, Pui-Yan, Riethman, Harold, Xiao, Ming
المصدر: Nucleic Acids Research. 45(9)
مصطلحات موضوعية: Biological Sciences, Bioinformatics and Computational Biology, Genetics, Human Genome, 1.1 Normal biological development and functioning, Generic health relevance, Automation, Chromosome Mapping, DNA, Feasibility Studies, Genetic Variation, Haplotypes, Humans, Repetitive Sequences, Nucleic Acid, Telomere, Environmental Sciences, Information and Computing Sciences, Developmental Biology, Biological sciences, Chemical sciences, Environmental sciences
وصف الملف: application/pdf
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13Academic Journal
المؤلفون: Narasimhan, Sharanya, Rajagopalan, Ramakrishnan, Justin Margret, Jeffrey, Visvanathan, Gnanaprakash, Jayasankaran, Chandru, Rekha, Kota, Srisailapathy, C. R. Srikumari
المساهمون: Tamil Nadu Pollution Control Board, UGC Research Scientist Scheme
المصدر: Hearing Balance and Communication ; volume 20, issue 1, page 21-31 ; ISSN 2169-5717
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14Periodical
المؤلفون: Walker, Roger C., Meddeb, Amira B., Perini, Steve, Furman, Eugene, Norrell, Michael, Woodward, William H., Person, Tim, Sengupta, Saurav, Rajagopalan, Ramakrishnan, Lanagan, Michael
المصدر: IEEE Transactions on Dielectrics and Electrical Insulation; October 2024, Vol. 31 Issue: 5 p2632-2641, 10p
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15Academic Journal
المؤلفون: Ganesh, Santhi K, Tragante, Vinicius, Guo, Wei, Guo, Yiran, Lanktree, Matthew B, Smith, Erin N, Johnson, Toby, Castillo, Berta Almoguera, Barnard, John, Baumert, Jens, Chang, Yen-Pei Christy, Elbers, Clara C, Farrall, Martin, Fischer, Mary E, Franceschini, Nora, Gaunt, Tom R, Gho, Johannes MIH, Gieger, Christian, Gong, Yan, Isaacs, Aaron, Kleber, Marcus E, Leach, Irene Mateo, McDonough, Caitrin W, Meijs, Matthijs FL, Mellander, Olle, Molony, Cliona M, Nolte, Ilja M, Padmanabhan, Sandosh, Price, Tom S, Rajagopalan, Ramakrishnan, Shaffer, Jonathan, Shah, Sonia, Shen, Haiqing, Soranzo, Nicole, van der Most, Peter J, Van Iperen, Erik PA, Van Setten, Jessic A, Vonk, Judith M, Zhang, Li, Beitelshees, Amber L, Berenson, Gerald S, Bhatt, Deepak L, Boer, Jolanda MA, Boerwinkle, Eric, Burkley, Ben, Burt, Amber, Chakravarti, Aravinda, Chen, Wei, Cooper-DeHoff, Rhonda M, Curtis, Sean P, Dreisbach, Albert, Duggan, David, Ehret, Georg B, Fabsitz, Richard R, Fornage, Myriam, Fox, Ervin, Furlong, Clement E, Gansevoort, Ron T, Hofker, Marten H, Hovingh, G Kees, Kirkland, Susan A, Kottke-Marchant, Kandice, Kutlar, Abdullah, LaCroix, Andrea Z, Langaee, Taimour Y, Li, Yun R, Lin, Honghuang, Liu, Kiang, Maiwald, Steffi, Malik, Rainer, Murugesan, Gurunathan, Newton-Cheh, Christopher, O'Connell, Jeffery R, Onland-Moret, N Charlotte, Ouwehand, Willem H, Palmas, Walter, Penninx, Brenda W, Pepine, Carl J, Pettinger, Mary, Polak, Joseph F, Ramachandran, Vasan S, Ranchalis, Jane, Redline, Susan, Ridker, Paul M, Rose, Lynda M, Scharnag, Hubert, Schork, Nicholas J, Shimbo, Daichi, Shuldiner, Alan R, Srinivasan, Sathanur R, Stolk, Ronald P, Taylor, Herman A, Thorand, Barbara, Trip, Mieke D, van Duijn, Cornelia M, Verschuren, W Monique, Wijmenga, Cisca, Winkelmann, Bernhard R, Wyatt, Sharon, Young, J Hunter
المصدر: Human Molecular Genetics. 22(8)
مصطلحات موضوعية: Hypertension, Heart Disease, Human Genome, Genetics, Clinical Research, Cardiovascular, Aetiology, 2.1 Biological and endogenous factors, Adult, Aged, Blood Pressure, Cardiovascular Diseases, Chromosome Mapping, Cohort Studies, Female, Genetic Predisposition to Disease, Genome-Wide Association Study, Genotype, Humans, Male, Middle Aged, Polymorphism, Single Nucleotide, White People, CARDIOGRAM, METASTROKE, LifeLines Cohort Study, Biological Sciences, Medical and Health Sciences, Genetics & Heredity
URL الوصول: https://escholarship.org/uc/item/16d246b2
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16Academic Journal
المؤلفون: Asselbergs, Folkert W, Guo, Yiran, van Iperen, Erik PA, Sivapalaratnam, Suthesh, Tragante, Vinicius, Lanktree, Matthew B, Lange, Leslie A, Almoguera, Berta, Appelman, Yolande E, Barnard, John, Baumert, Jens, Beitelshees, Amber L, Bhangale, Tushar R, Chen, Yii-Der Ida, Gaunt, Tom R, Gong, Yan, Hopewell, Jemma C, Johnson, Toby, Kleber, Marcus E, Langaee, Taimour Y, Li, Mingyao, Li, Yun R, Liu, Kiang, McDonough, Caitrin W, Meijs, Matthijs FL, Middelberg, Rita PS, Musunuru, Kiran, Nelson, Christopher P, O’Connell, Jeffery R, Padmanabhan, Sandosh, Pankow, James S, Pankratz, Nathan, Rafelt, Suzanne, Rajagopalan, Ramakrishnan, Romaine, Simon PR, Schork, Nicholas J, Shaffer, Jonathan, Shen, Haiqing, Smith, Erin N, Tischfield, Sam E, van der Most, Peter J, van Vliet-Ostaptchouk, Jana V, Verweij, Niek, Volcik, Kelly A, Zhang, Li, Bailey, Kent R, Bailey, Kristian M, Bauer, Florianne, Boer, Jolanda MA, Braund, Peter S, Burt, Amber, Burton, Paul R, Buxbaum, Sarah G, Chen, Wei, Cooper-DeHoff, Rhonda M, Cupples, L Adrienne, deJong, Jonas S, Delles, Christian, Duggan, David, Fornage, Myriam, Furlong, Clement E, Glazer, Nicole, Gums, John G, Hastie, Claire, Holmes, Michael V, Illig, Thomas, Kirkland, Susan A, Kivimaki, Mika, Klein, Ronald, Klein, Barbara E, Kooperberg, Charles, Kottke-Marchant, Kandice, Kumari, Meena, LaCroix, Andrea Z, Mallela, Laya, Murugesan, Gurunathan, Ordovas, Jose, Ouwehand, Willem H, Post, Wendy S, Saxena, Richa, Scharnagl, Hubert, Schreiner, Pamela J, Shah, Tina, Shields, Denis C, Shimbo, Daichi, Srinivasan, Sathanur R, Stolk, Ronald P, Swerdlow, Daniel I, Taylor, Herman A, Topol, Eric J, Toskala, Elina, van Pelt, Joost L, van Setten, Jessica, Yusuf, Salim, Whittaker, John C, Zwinderman, AH, Study, LifeLines Cohort, Anand, Sonia S, Balmforth, Anthony J, Berenson, Gerald S
المصدر: American Journal of Human Genetics. 91(5)
مصطلحات موضوعية: Biological Sciences, Biomedical and Clinical Sciences, Genetics, Epidemiology, Health Sciences, Human Genome, Atherosclerosis, Cholesterol, HDL, Cholesterol, LDL, Female, Genome-Wide Association Study, Genotype, Humans, Lipids, Male, Phenotype, Polymorphism, Single Nucleotide, Quantitative Trait Loci, Sex Factors, Triglycerides, White People, LifeLines Cohort Study, Medical and Health Sciences, Genetics & Heredity, Biological sciences, Biomedical and clinical sciences, Health sciences
URL الوصول: https://escholarship.org/uc/item/6tz7g5xd
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17Academic Journal
المؤلفون: Seo, Joo-Hwan, Fan, Zhongming, Nakaya, Hiroto, Rajagopalan, Ramakrishnan, Gomez, Enrique D., Iwasaki, Masato, Randall, Clive A.
المساهمون: NGK Spark Plug Co., Ltd.
المصدر: Japanese Journal of Applied Physics ; volume 60, issue 3, page 037001 ; ISSN 0021-4922 1347-4065
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18Academic Journal
المؤلفون: Rajagopalan, Ramakrishnan, Gilbert, Melissa A., McEldrew, Deborah A., Nassur, James A., Loomes, Kathleen M., Piccoli, David A., Krantz, Ian D., Conlin, Laura K., Spinner, Nancy B.
المصدر: Genetics in Medicine ; volume 23, issue 2, page 323-330 ; ISSN 1098-3600
الاتاحة: http://dx.doi.org/10.1038/s41436-020-00989-8
https://www.nature.com/articles/s41436-020-00989-8.pdf
https://www.nature.com/articles/s41436-020-00989-8
https://api.elsevier.com/content/article/PII:S1098360021025491?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S1098360021025491?httpAccept=text/plain -
19Academic Journal
المؤلفون: Lanktree, Matthew B, Guo, Yiran, Murtaza, Muhammed, Glessner, Joseph T, Bailey, Swneke D, Onland-Moret, N Charlotte, Lettre, Guillaume, Ongen, Halit, Rajagopalan, Ramakrishnan, Johnson, Toby, Shen, Haiqing, Nelson, Christopher P, Klopp, Norman, Baumert, Jens, Padmanabhan, Sandosh, Pankratz, Nathan, Pankow, James S, Shah, Sonia, Taylor, Kira, Barnard, John, Peters, Bas J, Maloney, Cliona M, Lobmeyer, Maximilian T, Stanton, Alice, Zafarmand, M Hadi, Romaine, Simon PR, Mehta, Amar, van Iperen, Erik PA, Gong, Yan, Price, Tom S, Smith, Erin N, Kim, Cecilia E, Li, Yun R, Asselbergs, Folkert W, Atwood, Larry D, Bailey, Kristian M, Bhatt, Deepak, Bauer, Florianne, Behr, Elijah R, Bhangale, Tushar, Boer, Jolanda MA, Boehm, Bernhard O, Bradfield, Jonathan P, Brown, Morris, Braund, Peter S, Burton, Paul R, Carty, Cara, Chandrupatla, Hareesh R, Chen, Wei, Connell, John, Dalgeorgou, Chrysoula, de Boer, Anthonius, Drenos, Fotios, Elbers, Clara C, Fang, James C, Fox, Caroline S, Frackelton, Edward C, Fuchs, Barry, Furlong, Clement E, Gibson, Quince, Gieger, Christian, Goel, Anuj, Grobbee, Diederik E, Hastie, Claire, Howard, Philip J, Huang, Guan-Hua, Johnson, W Craig, Li, Qing, Kleber, Marcus E, Klein, Barbara EK, Klein, Ronald, Kooperberg, Charles, Ky, Bonnie, LaCroix, Andrea, Lanken, Paul, Lathrop, Mark, Li, Mingyao, Marshall, Vanessa, Melander, Olle, Mentch, Frank D, Meyer, Nuala J, Monda, Keri L, Montpetit, Alexandre, Murugesan, Gurunathan, Nakayama, Karen, Nondahl, Dave, Onipinla, Abiodun, Rafelt, Suzanne, Newhouse, Stephen J, Otieno, F George, Patel, Sanjey R, Putt, Mary E, Rodriguez, Santiago, Safa, Radwan N, Sawyer, Douglas B, Schreiner, Pamela J, Simpson, Claire, Sivapalaratnam, Suthesh, Srinivasan, Sathanur R, Suver, Christine
المصدر: American Journal of Human Genetics. 88(1)
مصطلحات موضوعية: Epidemiology, Biological Sciences, Health Sciences, Genetics, Human Genome, 2.1 Biological and endogenous factors, Aetiology, Adult, Black or African American, Asian People, Body Height, Cardiovascular System, Female, Gene Frequency, Genetic Heterogeneity, Genetic Loci, Genome-Wide Association Study, Hispanic or Latino, Humans, Interleukin-11, Male, Polymorphism, Single Nucleotide, Smad3 Protein, White People, Hugh Watkins on behalf of PROCARDIS, Meena Kumari on behalf of the Whitehall II Study and the WHII 50K Group, Medical and Health Sciences, Genetics & Heredity, Biological sciences, Biomedical and clinical sciences, Health sciences
URL الوصول: https://escholarship.org/uc/item/9mk379qd
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20Academic Journal
المساهمون: National Human Genome Research Institute
المصدر: Genome Medicine ; volume 12, issue 1 ; ISSN 1756-994X