Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 25 to 33 of 33 entries
Sorted by: Best Match Show Resources per page
[CHROMOSOME ABNORMALITIES AND OLIGOPHRENIA].

Revista clinica espanola

ORTIZMANCHADO O, HERREROSFERNANDEZ B, BANUELOS J, VELASCOALONSO R, VILLACIANREBOLLO JM.
PMID: 14312931
Rev Clin Esp. 1965 Jan 31;96:93-7.

No abstract available.

Cite
ORTIZMANCHADO O, HERREROSFERNANDEZ B, BANUELOS J, et al. ANOMAL'IAS CROMOS'OMICAS Y OLIGOFRENIA. [CHROMOSOME ABNORMALITIES AND OLIGOPHRENIA]. Rev Clin Esp. 1965;96:93-7
ORTIZMANCHADO, O., HERREROSFERNANDEZ, B., BANUELOS, J., VELASCOALONSO, R., & VILLACIANREBOLLO, J. M. (1965). ANOMAL'IAS CROMOS'OMICAS Y OLIGOFRENIA. [CHROMOSOME ABNORMALITIES AND OLIGOPHRENIA]. Revista clinica espanola, 9693-7.
ORTIZMANCHADO, O, et al. "ANOMAL'IAS CROMOS'OMICAS Y OLIGOFRENIA." [CHROMOSOME ABNORMALITIES AND OLIGOPHRENIA]. Revista clinica espanola vol. 96 (1965): 93-7.
ORTIZMANCHADO O, HERREROSFERNANDEZ B, BANUELOS J, VELASCOALONSO R, VILLACIANREBOLLO JM. ANOMAL'IAS CROMOS'OMICAS Y OLIGOFRENIA. [CHROMOSOME ABNORMALITIES AND OLIGOPHRENIA]. Rev Clin Esp. 1965 Jan 31;96:93-7. Spanish. PMID: 14312931.
Copy Download .nbib Format: NLM
Intratumor diversity and clonal evolution in cancer--a skeptical standpoint.

Advances in cancer research

Gisselsson D.
PMID: 21925299
Adv Cancer Res. 2011;112:1-9. doi: 10.1016/B978-0-12-387688-1.00001-6.

Clonal evolution in cancer is intimately linked to the concept of intratumor cellular diversity, as the latter is a prerequisite for Darwinian selection at the micro-level. It has been frequently suggested in the literature that clonal evolution can be...

Cite
Gisselsson D. Intratumor diversity and clonal evolution in cancer--a skeptical standpoint. Adv Cancer Res. 2011;112:1-9doi: 10.1016/B978-0-12-387688-1.00001-6.
Gisselsson, D. (2011). Intratumor diversity and clonal evolution in cancer--a skeptical standpoint. Advances in cancer research, 1121-9. https://doi.org/10.1016/B978-0-12-387688-1.00001-6
Gisselsson, David. "Intratumor diversity and clonal evolution in cancer--a skeptical standpoint." Advances in cancer research vol. 112 (2011): 1-9. doi: https://doi.org/10.1016/B978-0-12-387688-1.00001-6
Gisselsson D. Intratumor diversity and clonal evolution in cancer--a skeptical standpoint. Adv Cancer Res. 2011;112:1-9. doi: 10.1016/B978-0-12-387688-1.00001-6. PMID: 21925299.
Copy Download .nbib Format: NLM
[The research progress on the effects of genetic damage induced by power frequency magnetic fields with harmful physical and chemical factors].

Zhonghua lao dong wei sheng zhi ye bing za zhi = Zhonghua laodong weisheng zhiyebing zazhi = Chinese journal of industrial hygiene and occupational diseases

Hua JN, Lv Y, Cheng Q.
PMID: 22804897
Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi. 2012 Mar;30(3):227-9.

No abstract available.

Cite
Hua JN, Lv Y, Cheng Q. [The research progress on the effects of genetic damage induced by power frequency magnetic fields with harmful physical and chemical factors]. Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi. 2012;30(3):227-9
Hua, J. N., Lv, Y., & Cheng, Q. (2012). [The research progress on the effects of genetic damage induced by power frequency magnetic fields with harmful physical and chemical factors]. Zhonghua lao dong wei sheng zhi ye bing za zhi = Zhonghua laodong weisheng zhiyebing zazhi = Chinese journal of industrial hygiene and occupational diseases, 30(3), 227-9.
Hua, Jia-ning, et al. "[The research progress on the effects of genetic damage induced by power frequency magnetic fields with harmful physical and chemical factors]." Zhonghua lao dong wei sheng zhi ye bing za zhi = Zhonghua laodong weisheng zhiyebing zazhi = Chinese journal of industrial hygiene and occupational diseases vol. 30,3 (2012): 227-9.
Hua JN, Lv Y, Cheng Q. [The research progress on the effects of genetic damage induced by power frequency magnetic fields with harmful physical and chemical factors]. Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi. 2012 Mar;30(3):227-9. Chinese. PMID: 22804897.
Copy Download .nbib Format: NLM
Symposium on chromosomes and neoplasia.

Human pathology

[No authors listed]
PMID: 7275091
Hum Pathol. 1981 Jun;12(6):493-549.

No abstract available.

Cite
Symposium on chromosomes and neoplasia. Hum Pathol. 1981;12(6):493-549
(1981). Symposium on chromosomes and neoplasia. Human pathology, 12(6), 493-549.
"Symposium on chromosomes and neoplasia." Human pathology vol. 12,6 (1981): 493-549.
Symposium on chromosomes and neoplasia. Hum Pathol. 1981 Jun;12(6):493-549. PMID: 7275091.
Copy Download .nbib Format: NLM
Cells with double minutes divided into two categories.

Cancer genetics and cytogenetics

Bullerdiek J, Bartnitzke S, Schloot W.
PMID: 6861119
Cancer Genet Cytogenet. 1983 Jul;9(3):301-4. doi: 10.1016/0165-4608(83)90014-6.

No abstract available.

Cite
Bullerdiek J, Bartnitzke S, Schloot W. Cells with double minutes divided into two categories. Cancer Genet Cytogenet. 1983;9(3):301-4doi: 10.1016/0165-4608(83)90014-6.
Bullerdiek, J., Bartnitzke, S., & Schloot, W. (1983). Cells with double minutes divided into two categories. Cancer genetics and cytogenetics, 9(3), 301-4. https://doi.org/10.1016/0165-4608(83)90014-6
Bullerdiek, J, et al. "Cells with double minutes divided into two categories." Cancer genetics and cytogenetics vol. 9,3 (1983): 301-4. doi: https://doi.org/10.1016/0165-4608(83)90014-6
Bullerdiek J, Bartnitzke S, Schloot W. Cells with double minutes divided into two categories. Cancer Genet Cytogenet. 1983 Jul;9(3):301-4. doi: 10.1016/0165-4608(83)90014-6. PMID: 6861119.
Copy Download .nbib Format: NLM
Turner's syndrome karyotypes.

JAMA

Gendel E.
PMID: 5107616
JAMA. 1971 Feb 15;215(7):1160. doi: 10.1001/jama.1971.03180200082037.

No abstract available.

Cite
Gendel E. Turner's syndrome karyotypes. JAMA. 1971;215(7):1160doi: 10.1001/jama.1971.03180200082037.
Gendel, E. (1971). Turner's syndrome karyotypes. JAMA, 215(7), 1160. https://doi.org/10.1001/jama.1971.03180200082037
Gendel, E. "Turner's syndrome karyotypes." JAMA vol. 215,7 (1971): 1160. doi: https://doi.org/10.1001/jama.1971.03180200082037
Gendel E. Turner's syndrome karyotypes. JAMA. 1971 Feb 15;215(7):1160. doi: 10.1001/jama.1971.03180200082037. PMID: 5107616.
Copy Download .nbib Format: NLM
Effective normalization for copy number variation in Hi-C data.

BMC bioinformatics

Servant N, Varoquaux N, Heard E, Barillot E, Vert JP.
PMID: 30189838
BMC Bioinformatics. 2018 Sep 06;19(1):313. doi: 10.1186/s12859-018-2256-5.

BACKGROUND: Normalization is essential to ensure accurate analysis and proper interpretation of sequencing data, and chromosome conformation capture data such as Hi-C have particular challenges. Although several methods have been proposed, the most widely used type of normalization of...

Cite
Servant N, Varoquaux N, Heard E, et al. Effective normalization for copy number variation in Hi-C data. BMC Bioinformatics. 2018;19(1):313doi: 10.1186/s12859-018-2256-5.
Servant, N., Varoquaux, N., Heard, E., Barillot, E., & Vert, J. P. (2018). Effective normalization for copy number variation in Hi-C data. BMC bioinformatics, 19(1), 313. https://doi.org/10.1186/s12859-018-2256-5
Servant, Nicolas, et al. "Effective normalization for copy number variation in Hi-C data." BMC bioinformatics vol. 19,1 (2018): 313. doi: https://doi.org/10.1186/s12859-018-2256-5
Servant N, Varoquaux N, Heard E, Barillot E, Vert JP. Effective normalization for copy number variation in Hi-C data. BMC Bioinformatics. 2018 Sep 06;19(1):313. doi: 10.1186/s12859-018-2256-5. PMID: 30189838; PMCID: PMC6127909.
Copy Download .nbib Format: NLM
A cross-comparison of cognitive ability across 8 genomic disorders.

Current opinion in genetics & development

Mortillo M, Mulle JG.
PMID: 34082144
Curr Opin Genet Dev. 2021 Jun;68:106-116. doi: 10.1016/j.gde.2021.04.001. Epub 2021 May 31.

Genomic disorders result from rearrangement of the human genome. Most genomic disorders are caused by copy number variants (CNV), deletions or duplications of several hundred kilobases. Many CNV loci are associated with autism, schizophrenia, and most commonly, intellectual disability...

Cite
Mortillo M, Mulle JG. A cross-comparison of cognitive ability across 8 genomic disorders. Curr Opin Genet Dev. 2021;68:106-116doi: 10.1016/j.gde.2021.04.001.
Mortillo, M., & Mulle, J. G. (2021). A cross-comparison of cognitive ability across 8 genomic disorders. Current opinion in genetics & development, 68106-116. https://doi.org/10.1016/j.gde.2021.04.001
Mortillo, Michael, and Mulle, Jennifer G. "A cross-comparison of cognitive ability across 8 genomic disorders." Current opinion in genetics & development vol. 68 (2021): 106-116. doi: https://doi.org/10.1016/j.gde.2021.04.001
Mortillo M, Mulle JG. A cross-comparison of cognitive ability across 8 genomic disorders. Curr Opin Genet Dev. 2021 Jun;68:106-116. doi: 10.1016/j.gde.2021.04.001. Epub 2021 May 31. PMID: 34082144; PMCID: PMC8259020.
Copy Download .nbib Format: NLM
Cytogenomic aberrations associated with prostate cancer.

Cancer genetics

Gu G, Brothman AR.
PMID: 21504704
Cancer Genet. 2011 Feb;204(2):57-67. doi: 10.1016/j.cancergencyto.2010.10.003.

Genetic changes associated with prostate cancer have finally begun to elucidate some of the mechanisms involved in the etiology of this complex and common disease. We highlight consistent and relatively frequent abnormalities seen by various methodologies. Specifically, the results...

Cite
Gu G, Brothman AR. Cytogenomic aberrations associated with prostate cancer. Cancer Genet. 2011;204(2):57-67doi: 10.1016/j.cancergencyto.2010.10.003.
Gu, G., & Brothman, A. R. (2011). Cytogenomic aberrations associated with prostate cancer. Cancer genetics, 204(2), 57-67. https://doi.org/10.1016/j.cancergencyto.2010.10.003
Gu, Guangyu, and Brothman, Arthur R. "Cytogenomic aberrations associated with prostate cancer." Cancer genetics vol. 204,2 (2011): 57-67. doi: https://doi.org/10.1016/j.cancergencyto.2010.10.003
Gu G, Brothman AR. Cytogenomic aberrations associated with prostate cancer. Cancer Genet. 2011 Feb;204(2):57-67. doi: 10.1016/j.cancergencyto.2010.10.003. PMID: 21504704.
Copy Download .nbib Format: NLM
Showing 25 to 33 of 33 entries