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Showing 25 to 36 of 64 entries
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Genomic mismatch scanning for the mapping of genetic traits.

Methods in molecular biology (Clifton, N.J.)

Mirzayans F, Walter MA.
PMID: 11462847
Methods Mol Biol. 2001;175:37-46. doi: 10.1385/1-59259-235-X:037.

No abstract available.

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Mirzayans F, Walter MA. Genomic mismatch scanning for the mapping of genetic traits. Methods Mol Biol. 2001;175:37-46doi: 10.1385/1-59259-235-X:037.
Mirzayans, F., & Walter, M. A. (2001). Genomic mismatch scanning for the mapping of genetic traits. Methods in molecular biology (Clifton, N.J.), 17537-46. https://doi.org/10.1385/1-59259-235-X:037
Mirzayans, F, and Walter, M A. "Genomic mismatch scanning for the mapping of genetic traits." Methods in molecular biology (Clifton, N.J.) vol. 175 (2001): 37-46. doi: https://doi.org/10.1385/1-59259-235-X:037
Mirzayans F, Walter MA. Genomic mismatch scanning for the mapping of genetic traits. Methods Mol Biol. 2001;175:37-46. doi: 10.1385/1-59259-235-X:037. PMID: 11462847.
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[Genetic mapping].

Ugeskrift for laeger

Nørby S.
PMID: 11014148
Ugeskr Laeger. 2000 Sep 18;162(38):5102-3.

No abstract available.

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Nørby S. Genetiske mappemaend. [Genetic mapping]. Ugeskr Laeger. 2000;162(38):5102-3
Nørby, S. (2000). Genetiske mappemaend. [Genetic mapping]. Ugeskrift for laeger, 162(38), 5102-3.
Nørby, S. "Genetiske mappemaend." [Genetic mapping]. Ugeskrift for laeger vol. 162,38 (2000): 5102-3.
Nørby S. Genetiske mappemaend. [Genetic mapping]. Ugeskr Laeger. 2000 Sep 18;162(38):5102-3. Danish. PMID: 11014148.
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[The quality of genetic association studies need to be improved].

Zhonghua xin xue guan bing za zhi

GU DF.
PMID: 19134268
Zhonghua Xin Xue Guan Bing Za Zhi. 2008 Dec;36(12):1057-8.

No abstract available.

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GU DF. [The quality of genetic association studies need to be improved]. Zhonghua Xin Xue Guan Bing Za Zhi. 2008;36(12):1057-8
GU, D. F. (2008). [The quality of genetic association studies need to be improved]. Zhonghua xin xue guan bing za zhi, 36(12), 1057-8.
GU, Dong-Feng. "[The quality of genetic association studies need to be improved]." Zhonghua xin xue guan bing za zhi vol. 36,12 (2008): 1057-8.
GU DF. [The quality of genetic association studies need to be improved]. Zhonghua Xin Xue Guan Bing Za Zhi. 2008 Dec;36(12):1057-8. Chinese. PMID: 19134268.
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Channeling DNA for optical mapping.

Nature biotechnology

Michaeli Y, Ebenstein Y.
PMID: 22871713
Nat Biotechnol. 2012 Aug;30(8):762-3. doi: 10.1038/nbt.2324.

No abstract available.

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Michaeli Y, Ebenstein Y. Channeling DNA for optical mapping. Nat Biotechnol. 2012;30(8):762-3doi: 10.1038/nbt.2324.
Michaeli, Y., & Ebenstein, Y. (2012). Channeling DNA for optical mapping. Nature biotechnology, 30(8), 762-3. https://doi.org/10.1038/nbt.2324
Michaeli, Yael, and Ebenstein, Yuval. "Channeling DNA for optical mapping." Nature biotechnology vol. 30,8 (2012): 762-3. doi: https://doi.org/10.1038/nbt.2324
Michaeli Y, Ebenstein Y. Channeling DNA for optical mapping. Nat Biotechnol. 2012 Aug;30(8):762-3. doi: 10.1038/nbt.2324. PMID: 22871713.
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[Systemic lupus erythematosus: genomics of the disease].

Gaceta medica de Mexico

Velázquez-Cruz R, Jiménez-Morales S, Ramírez-Bello J, Aguilar-Delfín I, Salas-Martínez G, Baca Ruíz V, Orozco Orozco L.
PMID: 22976755
Gac Med Mex. 2012 Jul-Aug;148(4):371-80.

Systemic lupus erythematosus (SLE) is the prototype of autoimmune diseases with multiple autoantigens as targets,resulting in damage to many organs of the body. The disease is more common in females (> 90%) and around 15% of the cases present...

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Velázquez-Cruz R, Jiménez-Morales S, Ramírez-Bello J, et al. Lupus eritematoso sistémico (LES): genómica de la enfermedad. [Systemic lupus erythematosus: genomics of the disease]. Gac Med Mex. 2012;148(4):371-80
Velázquez-Cruz, R., Jiménez-Morales, S., Ramírez-Bello, J., Aguilar-Delfín, I., Salas-Martínez, G., Baca Ruíz, V., & Orozco Orozco, L. (2012). Lupus eritematoso sistémico (LES): genómica de la enfermedad. [Systemic lupus erythematosus: genomics of the disease]. Gaceta medica de Mexico, 148(4), 371-80.
Velázquez-Cruz, Rafael, et al. "Lupus eritematoso sistémico (LES): genómica de la enfermedad." [Systemic lupus erythematosus: genomics of the disease]. Gaceta medica de Mexico vol. 148,4 (2012): 371-80.
Velázquez-Cruz R, Jiménez-Morales S, Ramírez-Bello J, Aguilar-Delfín I, Salas-Martínez G, Baca Ruíz V, Orozco Orozco L. Lupus eritematoso sistémico (LES): genómica de la enfermedad. [Systemic lupus erythematosus: genomics of the disease]. Gac Med Mex. 2012 Jul-Aug;148(4):371-80. Spanish. PMID: 22976755.
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Interacting with Genomic Data: Clinician Requirements and Prototype Structure.

Studies in health technology and informatics

Bradford D, Berkovsky S, Martyn M, Bakkar T, Krahnert M, Rodriguez M, Bauer D, Ireland D, Gaff C.
PMID: 28756429
Stud Health Technol Inform. 2017;239:1-7.

Healthcare is currently being transformed by the introduction of genomic sequencing - a major advancement in personalised medicine. This advent provides new opportunities for clinicians to use genomic data in decision making about patient diagnosis and treatment, but this...

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Bradford D, Berkovsky S, Martyn M, et al. Interacting with Genomic Data: Clinician Requirements and Prototype Structure. Stud Health Technol Inform. 2017;239:1-7
Bradford, D., Berkovsky, S., Martyn, M., Bakkar, T., Krahnert, M., Rodriguez, M., Bauer, D., Ireland, D., & Gaff, C. (2017). Interacting with Genomic Data: Clinician Requirements and Prototype Structure. Studies in health technology and informatics, 2391-7.
Bradford, Dana, et al. "Interacting with Genomic Data: Clinician Requirements and Prototype Structure." Studies in health technology and informatics vol. 239 (2017): 1-7.
Bradford D, Berkovsky S, Martyn M, Bakkar T, Krahnert M, Rodriguez M, Bauer D, Ireland D, Gaff C. Interacting with Genomic Data: Clinician Requirements and Prototype Structure. Stud Health Technol Inform. 2017;239:1-7. PMID: 28756429.
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Reporting of race in genome and exome sequencing studies of cancer: a scoping review of the literature.

Genetics in medicine : official journal of the American College of Medical Genetics

Nugent A, Conatser KR, Turner LL, Nugent JT, Sarino EMB, Ricks-Santi LJ.
PMID: 31160752
Genet Med. 2019 Dec;21(12):2676-2680. doi: 10.1038/s41436-019-0558-2. Epub 2019 Jun 04.

PURPOSE: Minorities are often underrepresented in clinical cancer research yet the frequency of reporting of race in genomic sequencing studies of cancer is unknown. This scoping review determines the rate at which race is reported as a demographic variable,...

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Nugent A, Conatser KR, Turner LL, et al. Reporting of race in genome and exome sequencing studies of cancer: a scoping review of the literature. Genet Med. 2019;21(12):2676-2680doi: 10.1038/s41436-019-0558-2.
Nugent, A., Conatser, K. R., Turner, L. L., Nugent, J. T., Sarino, E. M. B., & Ricks-Santi, L. J. (2019). Reporting of race in genome and exome sequencing studies of cancer: a scoping review of the literature. Genetics in medicine : official journal of the American College of Medical Genetics, 21(12), 2676-2680. https://doi.org/10.1038/s41436-019-0558-2
Nugent, Adrienne, et al. "Reporting of race in genome and exome sequencing studies of cancer: a scoping review of the literature." Genetics in medicine : official journal of the American College of Medical Genetics vol. 21,12 (2019): 2676-2680. doi: https://doi.org/10.1038/s41436-019-0558-2
Nugent A, Conatser KR, Turner LL, Nugent JT, Sarino EMB, Ricks-Santi LJ. Reporting of race in genome and exome sequencing studies of cancer: a scoping review of the literature. Genet Med. 2019 Dec;21(12):2676-2680. doi: 10.1038/s41436-019-0558-2. Epub 2019 Jun 04. PMID: 31160752; PMCID: PMC6891161.
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Multipoint genomic scanning for quantitative loci: effects of map density, sibship size and computational approach.

European journal of human genetics : EJHG

Goldgar DE, Shugart YY.
PMID: 10196691
Eur J Hum Genet. 1999 Feb-Mar;7(2):103-9. doi: 10.1038/sj.ejhg.5200280.

Multipoint interval mapping (MIM) and the MAPMAKER/SIBS program (M/S) are two methods of mapping quantitative loci by examining identity by descent (IBD) sharing in a region spanned by multiple microsatellite DNA markers. For the purpose of comparison, we simulated...

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Goldgar DE, Shugart YY. Multipoint genomic scanning for quantitative loci: effects of map density, sibship size and computational approach. Eur J Hum Genet. 1999;7(2):103-9doi: 10.1038/sj.ejhg.5200280.
Goldgar, D. E., & Shugart, Y. Y. (1999). Multipoint genomic scanning for quantitative loci: effects of map density, sibship size and computational approach. European journal of human genetics : EJHG, 7(2), 103-9. https://doi.org/10.1038/sj.ejhg.5200280
Goldgar, D E, and Shugart, Y Y. "Multipoint genomic scanning for quantitative loci: effects of map density, sibship size and computational approach." European journal of human genetics : EJHG vol. 7,2 (1999): 103-9. doi: https://doi.org/10.1038/sj.ejhg.5200280
Goldgar DE, Shugart YY. Multipoint genomic scanning for quantitative loci: effects of map density, sibship size and computational approach. Eur J Hum Genet. 1999 Feb-Mar;7(2):103-9. doi: 10.1038/sj.ejhg.5200280. PMID: 10196691.
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Tracing quantitative measurements on human chromosomes in family studies.

Annals of human genetics

Lauder IJ.
PMID: 921220
Ann Hum Genet. 1977 Jul;41(1):77-86. doi: 10.1111/j.1469-1809.1977.tb01963.x.

Statistical methods are developed for tracing quantitative measurements on human chromosomes from parents to offspring. Tests for transmission are briefly considered.

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Lauder IJ. Tracing quantitative measurements on human chromosomes in family studies. Ann Hum Genet. 1977;41(1):77-86doi: 10.1111/j.1469-1809.1977.tb01963.x.
Lauder, I. J. (1977). Tracing quantitative measurements on human chromosomes in family studies. Annals of human genetics, 41(1), 77-86. https://doi.org/10.1111/j.1469-1809.1977.tb01963.x
Lauder, I J. "Tracing quantitative measurements on human chromosomes in family studies." Annals of human genetics vol. 41,1 (1977): 77-86. doi: https://doi.org/10.1111/j.1469-1809.1977.tb01963.x
Lauder IJ. Tracing quantitative measurements on human chromosomes in family studies. Ann Hum Genet. 1977 Jul;41(1):77-86. doi: 10.1111/j.1469-1809.1977.tb01963.x. PMID: 921220.
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Human gene mapping 8. Helsinki conference (1985). Eighth International Workshop on Human Gene Mapping. Helsinki, Finland, August 4-10, 1985.

Cytogenetics and cell genetics

[No authors listed]
PMID: 4064765
Cytogenet Cell Genet. 1985;40(1):1-823.

No abstract available.

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Human gene mapping 8. Helsinki conference (1985). Eighth International Workshop on Human Gene Mapping. Helsinki, Finland, August 4-10, 1985. Cytogenet Cell Genet. 1985;40(1):1-823
(1985). Human gene mapping 8. Helsinki conference (1985). Eighth International Workshop on Human Gene Mapping. Helsinki, Finland, August 4-10, 1985. Cytogenetics and cell genetics, 40(1), 1-823.
"Human gene mapping 8. Helsinki conference (1985). Eighth International Workshop on Human Gene Mapping. Helsinki, Finland, August 4-10, 1985." Cytogenetics and cell genetics vol. 40,1 (1985): 1-823.
Human gene mapping 8. Helsinki conference (1985). Eighth International Workshop on Human Gene Mapping. Helsinki, Finland, August 4-10, 1985. Cytogenet Cell Genet. 1985;40(1):1-823. PMID: 4064765.
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A summary of the human gene map, 1973-1977.

Cytogenetics and cell genetics

Donald LJ, Hamerton JL.
PMID: 752529
Cytogenet Cell Genet. 1978;22(1):5-11. doi: 10.1159/000130914.

No abstract available.

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Donald LJ, Hamerton JL. A summary of the human gene map, 1973-1977. Cytogenet Cell Genet. 1978;22(1):5-11doi: 10.1159/000130914.
Donald, L. J., & Hamerton, J. L. (1978). A summary of the human gene map, 1973-1977. Cytogenetics and cell genetics, 22(1), 5-11. https://doi.org/10.1159/000130914
Donald, L J, and Hamerton, J L. "A summary of the human gene map, 1973-1977." Cytogenetics and cell genetics vol. 22,1 (1978): 5-11. doi: https://doi.org/10.1159/000130914
Donald LJ, Hamerton JL. A summary of the human gene map, 1973-1977. Cytogenet Cell Genet. 1978;22(1):5-11. doi: 10.1159/000130914. PMID: 752529.
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Peter John Langford Cook, 6 August 1939-23 January 1982.

Birth defects original article series

Robson EB.
PMID: 6760923
Birth Defects Orig Artic Ser. 1982;18(2):5-6.

No abstract available.

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Robson EB. Peter John Langford Cook, 6 August 1939-23 January 1982. Birth Defects Orig Artic Ser. 1982;18(2):5-6
Robson, E. B. (1982). Peter John Langford Cook, 6 August 1939-23 January 1982. Birth defects original article series, 18(2), 5-6.
Robson, E B. "Peter John Langford Cook, 6 August 1939-23 January 1982." Birth defects original article series vol. 18,2 (1982): 5-6.
Robson EB. Peter John Langford Cook, 6 August 1939-23 January 1982. Birth Defects Orig Artic Ser. 1982;18(2):5-6. PMID: 6760923.
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Showing 25 to 36 of 64 entries