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Showing 1 to 12 of 33 entries
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Direct effect of preferential segregation on the origin of polysomy.

Nature

SHULT EE, LINDEGREN CC.
PMID: 13418767
Nature. 1957 Mar 30;179(4561):683. doi: 10.1038/179683a0.

No abstract available.

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SHULT EE, LINDEGREN CC. Direct effect of preferential segregation on the origin of polysomy. Nature. 1957;179(4561):683doi: 10.1038/179683a0.
SHULT, E. E., & LINDEGREN, C. C. (1957). Direct effect of preferential segregation on the origin of polysomy. Nature, 179(4561), 683. https://doi.org/10.1038/179683a0
SHULT, E E, and LINDEGREN, C C. "Direct effect of preferential segregation on the origin of polysomy." Nature vol. 179,4561 (1957): 683. doi: https://doi.org/10.1038/179683a0
SHULT EE, LINDEGREN CC. Direct effect of preferential segregation on the origin of polysomy. Nature. 1957 Mar 30;179(4561):683. doi: 10.1038/179683a0. PMID: 13418767.
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Routine genetic testing for Asperger syndrome.

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

Chodirker BN, Chudley AE.
PMID: 18941416
Genet Med. 2008 Nov;10(11):843-5; author reply 845. doi: 10.1097/GIM.0b013e31818b0c76.

No abstract available.

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Chodirker BN, Chudley AE. Routine genetic testing for Asperger syndrome. Genet Med. 2008;10(11):843-5; author reply 845doi: 10.1097/GIM.0b013e31818b0c76.
Chodirker, B. N., & Chudley, A. E. (2008). Routine genetic testing for Asperger syndrome. Genetics in medicine : official journal of the American College of Medical Genetics, 10(11), 843-5; author reply 845. https://doi.org/10.1097/GIM.0b013e31818b0c76
Chodirker, Bernard N, and Chudley, Albert E. "Routine genetic testing for Asperger syndrome." Genetics in medicine : official journal of the American College of Medical Genetics vol. 10,11 (2008): 843-5; author reply 845. doi: https://doi.org/10.1097/GIM.0b013e31818b0c76
Chodirker BN, Chudley AE. Routine genetic testing for Asperger syndrome. Genet Med. 2008 Nov;10(11):843-5; author reply 845. doi: 10.1097/GIM.0b013e31818b0c76. PMID: 18941416.
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What do cytogenetic abnormalities after autotransplant really mean?.

Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation

Rossi G, Gale RP.
PMID: 25128616
Biol Blood Marrow Transplant. 2014 Nov;20(11):1870-1. doi: 10.1016/j.bbmt.2014.08.006. Epub 2014 Aug 14.

No abstract available.

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Rossi G, Gale RP. What do cytogenetic abnormalities after autotransplant really mean?. Biol Blood Marrow Transplant. 2014;20(11):1870-1doi: 10.1016/j.bbmt.2014.08.006.
Rossi, G., & Gale, R. P. (2014). What do cytogenetic abnormalities after autotransplant really mean?. Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 20(11), 1870-1. https://doi.org/10.1016/j.bbmt.2014.08.006
Rossi, Giuseppe, and Gale, Robert Peter. "What do cytogenetic abnormalities after autotransplant really mean?." Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation vol. 20,11 (2014): 1870-1. doi: https://doi.org/10.1016/j.bbmt.2014.08.006
Rossi G, Gale RP. What do cytogenetic abnormalities after autotransplant really mean?. Biol Blood Marrow Transplant. 2014 Nov;20(11):1870-1. doi: 10.1016/j.bbmt.2014.08.006. Epub 2014 Aug 14. PMID: 25128616.
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Cytogenetic analysis of tumor clonality.

Advances in cancer research

Teixeira MR, Heim S.
PMID: 21925303
Adv Cancer Res. 2011;112:127-49. doi: 10.1016/B978-0-12-387688-1.00005-3.

All or almost all neoplasias subjected to systematic cytogenetic scrutiny have been found to harbor acquired chromosomal aberrations. The paradigm stemming from the study of hematopoietic malignancies and sarcomas is that cancers are of monoclonal origin (i.e., they have...

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Teixeira MR, Heim S. Cytogenetic analysis of tumor clonality. Adv Cancer Res. 2011;112:127-49doi: 10.1016/B978-0-12-387688-1.00005-3.
Teixeira, M. R., & Heim, S. (2011). Cytogenetic analysis of tumor clonality. Advances in cancer research, 112127-49. https://doi.org/10.1016/B978-0-12-387688-1.00005-3
Teixeira, Manuel R, and Heim, Sverre. "Cytogenetic analysis of tumor clonality." Advances in cancer research vol. 112 (2011): 127-49. doi: https://doi.org/10.1016/B978-0-12-387688-1.00005-3
Teixeira MR, Heim S. Cytogenetic analysis of tumor clonality. Adv Cancer Res. 2011;112:127-49. doi: 10.1016/B978-0-12-387688-1.00005-3. PMID: 21925303.
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Evaluation of non-invasive prenatal testing to detect chromosomal aberrations in a Chinese cohort.

Journal of cellular and molecular medicine

Cui W, Liu X, Zhang Y, Wang Y, Chu G, He R, Zhao Y.
PMID: 31454164
J Cell Mol Med. 2019 Nov;23(11):7873-7878. doi: 10.1111/jcmm.14614. Epub 2019 Aug 27.

The aim of this study was to evaluate the clinical feasibility of non-invasive prenatal testing (NIPT) to detect foetal copy number variations (CNVs). Next-generation sequencing for detecting foetal copy number variations (CNVs) was performed on the collected samples from...

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Cui W, Liu X, Zhang Y, et al. Evaluation of non-invasive prenatal testing to detect chromosomal aberrations in a Chinese cohort. J Cell Mol Med. 2019;23(11):7873-7878doi: 10.1111/jcmm.14614.
Cui, W., Liu, X., Zhang, Y., Wang, Y., Chu, G., He, R., & Zhao, Y. (2019). Evaluation of non-invasive prenatal testing to detect chromosomal aberrations in a Chinese cohort. Journal of cellular and molecular medicine, 23(11), 7873-7878. https://doi.org/10.1111/jcmm.14614
Cui, Wanting, et al. "Evaluation of non-invasive prenatal testing to detect chromosomal aberrations in a Chinese cohort." Journal of cellular and molecular medicine vol. 23,11 (2019): 7873-7878. doi: https://doi.org/10.1111/jcmm.14614
Cui W, Liu X, Zhang Y, Wang Y, Chu G, He R, Zhao Y. Evaluation of non-invasive prenatal testing to detect chromosomal aberrations in a Chinese cohort. J Cell Mol Med. 2019 Nov;23(11):7873-7878. doi: 10.1111/jcmm.14614. Epub 2019 Aug 27. PMID: 31454164; PMCID: PMC6815821.
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[Application of single nucleotide polymorphism microarray in clinical diagnosis of intellectual disability or retardation].

Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences

Hu J, Qian Y, Sun Y, Yu J, Luo Y, Dong M.
PMID: 31901047
Zhejiang Da Xue Xue Bao Yi Xue Ban. 2019 Jun 25;48(4):420-428.

OBJECTIVE: To assess the clinical application of single nucleotide polymorphism microarray (SNP array) in patients with intellectual disability/developmental delay(ID/DD).METHODS: SNP array was performed to detect genome-wide DNA copy number variants (CNVs) for 145 patients with ID/DD in Women's Hospital,...

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Hu J, Qian Y, Sun Y, et al. [Application of single nucleotide polymorphism microarray in clinical diagnosis of intellectual disability or retardation]. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2019;48(4):420-428
Hu, J., Qian, Y., Sun, Y., Yu, J., Luo, Y., & Dong, M. (2019). [Application of single nucleotide polymorphism microarray in clinical diagnosis of intellectual disability or retardation]. Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences, 48(4), 420-428.
Hu, Junjie, et al. "[Application of single nucleotide polymorphism microarray in clinical diagnosis of intellectual disability or retardation]." Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences vol. 48,4 (2019): 420-428.
Hu J, Qian Y, Sun Y, Yu J, Luo Y, Dong M. [Application of single nucleotide polymorphism microarray in clinical diagnosis of intellectual disability or retardation]. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2019 Jun 25;48(4):420-428. Chinese. PMID: 31901047.
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Adaptive classifiers for dicentric chromosomes.

Journal of radiation research

Piper J, Sprey J.
PMID: 1507167
J Radiat Res. 1992 Mar;33:159-70. doi: 10.1269/jrr.33.supplement_159.
Free Article

Classification of dicentric chromosomes in a practical automatic screening system comprises three stages. The first generates plausible centromere candidates from each chromosome in an automatically segmented metaphase, and uses contextual knowledge to generate distributions of "probably true" and "probably...

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Piper J, Sprey J. Adaptive classifiers for dicentric chromosomes. J Radiat Res. 1992;33:159-70doi: 10.1269/jrr.33.supplement_159.
Piper, J., & Sprey, J. (1992). Adaptive classifiers for dicentric chromosomes. Journal of radiation research, 33159-70. https://doi.org/10.1269/jrr.33.supplement_159
Piper, J, and Sprey, J. "Adaptive classifiers for dicentric chromosomes." Journal of radiation research vol. 33 (1992): 159-70. doi: https://doi.org/10.1269/jrr.33.supplement_159
Piper J, Sprey J. Adaptive classifiers for dicentric chromosomes. J Radiat Res. 1992 Mar;33:159-70. doi: 10.1269/jrr.33.supplement_159. PMID: 1507167.
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Cytogenetic abnormalities in lung cancer.

Cancer treatment and research

Campbell L, Brown J, Garson OM, Morstyn G.
PMID: 2577168
Cancer Treat Res. 1989;45:123-36. doi: 10.1007/978-1-4613-1593-3_8.

No abstract available.

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Campbell L, Brown J, Garson OM, et al. Cytogenetic abnormalities in lung cancer. Cancer Treat Res. 1989;45:123-36doi: 10.1007/978-1-4613-1593-3_8.
Campbell, L., Brown, J., Garson, O. M., & Morstyn, G. (1989). Cytogenetic abnormalities in lung cancer. Cancer treatment and research, 45123-36. https://doi.org/10.1007/978-1-4613-1593-3_8
Campbell, L, et al. "Cytogenetic abnormalities in lung cancer." Cancer treatment and research vol. 45 (1989): 123-36. doi: https://doi.org/10.1007/978-1-4613-1593-3_8
Campbell L, Brown J, Garson OM, Morstyn G. Cytogenetic abnormalities in lung cancer. Cancer Treat Res. 1989;45:123-36. doi: 10.1007/978-1-4613-1593-3_8. PMID: 2577168.
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Monitoring of genetic instability in subjects with increased risk of cancer.

Annali dell'Istituto superiore di sanita

Nuzzo F, Stefanini M.
PMID: 2751199
Ann Ist Super Sanita. 1989;25(1):81-9.

Results of investigations performed to obtain data on genomic instability in subjects with increased risk of cancer are reported. People at risk for environmental or genetic factors included in this study were: 1) individuals from the Seveso population exposed...

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Nuzzo F, Stefanini M. Monitoring of genetic instability in subjects with increased risk of cancer. Ann Ist Super Sanita. 1989;25(1):81-9
Nuzzo, F., & Stefanini, M. (1989). Monitoring of genetic instability in subjects with increased risk of cancer. Annali dell'Istituto superiore di sanita, 25(1), 81-9.
Nuzzo, F, and Stefanini, M. "Monitoring of genetic instability in subjects with increased risk of cancer." Annali dell'Istituto superiore di sanita vol. 25,1 (1989): 81-9.
Nuzzo F, Stefanini M. Monitoring of genetic instability in subjects with increased risk of cancer. Ann Ist Super Sanita. 1989;25(1):81-9. PMID: 2751199.
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Letter: Do only a few chromosomes carry genes of prime importance for malignant transformation?.

Lancet (London, England)

Mitelman F, Levan G.
PMID: 59288
Lancet. 1976 Jul 31;2(7979):264. doi: 10.1016/s0140-6736(76)91076-x.

No abstract available.

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Mitelman F, Levan G. Letter: Do only a few chromosomes carry genes of prime importance for malignant transformation?. Lancet. 1976;2(7979):264doi: 10.1016/s0140-6736(76)91076-x.
Mitelman, F., & Levan, G. (1976). Letter: Do only a few chromosomes carry genes of prime importance for malignant transformation?. Lancet (London, England), 2(7979), 264. https://doi.org/10.1016/s0140-6736(76)91076-x
Mitelman, F, and Levan, G. "Letter: Do only a few chromosomes carry genes of prime importance for malignant transformation?." Lancet (London, England) vol. 2,7979 (1976): 264. doi: https://doi.org/10.1016/s0140-6736(76)91076-x
Mitelman F, Levan G. Letter: Do only a few chromosomes carry genes of prime importance for malignant transformation?. Lancet. 1976 Jul 31;2(7979):264. doi: 10.1016/s0140-6736(76)91076-x. PMID: 59288.
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On the localization of genes on certain autosomes of man through chromosome aberrations. 3. Exclusion of the possibility of gene assignment.

Humangenetik

Bender K, Burckhardt K.
PMID: 5488998
Humangenetik. 1970;9(1):75-85. doi: 10.1007/BF00696016.

No abstract available.

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Bender K, Burckhardt K. On the localization of genes on certain autosomes of man through chromosome aberrations. 3. Exclusion of the possibility of gene assignment. Humangenetik. 1970;9(1):75-85doi: 10.1007/BF00696016.
Bender, K., & Burckhardt, K. (1970). On the localization of genes on certain autosomes of man through chromosome aberrations. 3. Exclusion of the possibility of gene assignment. Humangenetik, 9(1), 75-85. https://doi.org/10.1007/BF00696016
Bender, K, and Burckhardt, K. "On the localization of genes on certain autosomes of man through chromosome aberrations. 3. Exclusion of the possibility of gene assignment." Humangenetik vol. 9,1 (1970): 75-85. doi: https://doi.org/10.1007/BF00696016
Bender K, Burckhardt K. On the localization of genes on certain autosomes of man through chromosome aberrations. 3. Exclusion of the possibility of gene assignment. Humangenetik. 1970;9(1):75-85. doi: 10.1007/BF00696016. PMID: 5488998.
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Y-CHROMOSOME DE NOVO RECOMBINANTS. IMPLICATIONS FOR NOMENCLATURE.

Genetic counseling (Geneva, Switzerland)

Rivera H.
PMID: 27192897
Genet Couns. 2016;27(1):91-3.

No abstract available.

Cite
Rivera H. Y-CHROMOSOME DE NOVO RECOMBINANTS. IMPLICATIONS FOR NOMENCLATURE. Genet Couns. 2016;27(1):91-3
Rivera, H. (2016). Y-CHROMOSOME DE NOVO RECOMBINANTS. IMPLICATIONS FOR NOMENCLATURE. Genetic counseling (Geneva, Switzerland), 27(1), 91-3.
Rivera, H. "Y-CHROMOSOME DE NOVO RECOMBINANTS. IMPLICATIONS FOR NOMENCLATURE." Genetic counseling (Geneva, Switzerland) vol. 27,1 (2016): 91-3.
Rivera H. Y-CHROMOSOME DE NOVO RECOMBINANTS. IMPLICATIONS FOR NOMENCLATURE. Genet Couns. 2016;27(1):91-3. PMID: 27192897.
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Showing 1 to 12 of 33 entries