William Rees Brebner Robertson (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "William Rees Brebner Robertson" in English language version.

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11doi.org

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10nih.gov

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1harvard.edu

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doi.org

Robertson, W. R. B.; Bohren, B. B.; Warren, D. C. (1943). "The Inheritance of Plumage in the Turkey". Journal of Heredity. 34 (8): 246–256. doi:10.1093/oxfordjournals.jhered.a105298.
Robertson, W.R.B. (1916). "Chromosome studies. I. Taxonomic relationships shown in the chromosomes of Tettigidae and Acrididae. V-shaped chromosomes and their significance in Acrididae, Locustidae and Gryllidae: chromosome and variation". Journal of Morphology. 27 (2): 179–331. doi:10.1002/jmor.1050270202. S2CID 86497936.
Nabors, R.K. (January 30, 1942). "Obituary: William Rees Brebner Robertson (1881-1941)". Science. 95 (2457): 113–114. doi:10.1126/science.95.2457.113. PMID 17795644.
Therman, E (February 1989). "The nonrandom participation of human afrocentric chromosomes in Robertsonian translocations". Annals of Human Genetics. 53 (53(Pt1)): 49–65. doi:10.1111/j.1469-1809.1989.tb01121.x. PMID 2658738. S2CID 1949436.
Zhao, WW (May 1, 2015). "Robertsonian Translocations: An Overview of 872 Robertsonian Translocations Identified in a Diagnostic Laboratory in China". PLOS ONE. 10 (5): e0122647. Bibcode:2015PLoSO..1022647Z. doi:10.1371/journal.pone.0122647. PMC 4416705. PMID 25932913.
Dolskiy, Alexander A.; Lemskaya, Natalya A.; Maksimova, Yulia V.; Shorina, Asia R.; Kolesnikova, Irina S.; Yudkin, Dmitry V. (2018). "Robertsonian translocation 13/14 associated with rRNA genes overexpression and intellectual disability". Egyptian Journal of Medical Human Genetics. 19 (2): 141–145. doi:10.1016/j.ejmhg.2017.11.002.
Engels, Hartmut; Eggermann, Thomas; Caliebe, Almut; Jelska, Anna; Schubert, Regine; Schüler, Herdit M.; Panasiuk, Barbara; Zaremba, Jacek; Latos-BieleńSka, Anna; Jakubowski, Lucjusz; Zerres, Klaus P.; Schwanitz, Gesa; Midro, Alina T. (2008). "Genetic counseling in Robertsonian translocations der(13;14): Frequencies of reproductive outcomes and infertility in 101 pedigrees**". American Journal of Medical Genetics Part A. 146A (20): 2611–2616. doi:10.1002/ajmg.a.32500. PMID 18798317. S2CID 42829871.
RACHISAN AL; NICULAE AS; TINTEA I; POP B; MILITARU M; BIZO A; HRUSCA A (2017). "Association of fragile X syndrome, Robertsonian translocation (13, 22) and autism in a child". Clujul Medical. 90 (4): 445–448. doi:10.15386/cjmed-763. PMC 5683837. PMID 29151796.
Buoni, S.; Zannolli, R.; MacUcci, F.; Pucci, L.; Mogni, M.; Pierluigi, M.; Fois, A. (2006). "Familial robertsonian 13;14 translocation with mental retardation and epilepsy". Journal of Child Neurology. 21 (6): 531–3. doi:10.1177/08830738060210060701. PMID 16948942. S2CID 44812342.
Jung, Moses (1940). "Modern Marriage". American Journal of Sociology. 47 (2). New York: F.S. Crofts & Company: 183–230. doi:10.1086/218887.
Bidau, Claudio J.; Martí, Dardo A. (2010). "110 Years of Orthopteran Cytogenetics, the Chromosomal Evolutionary Viewpoint, and Michael White's Signal Contributions to the Field". Journal of Orthoptera Research. 19 (2): 165–182. doi:10.1665/034.019.0202. hdl:11336/59292. S2CID 84319868.

findagrave.com

"William Rees Brebner Robertson". Find a Grave.

handle.net

hdl.handle.net

Bidau, Claudio J.; Martí, Dardo A. (2010). "110 Years of Orthopteran Cytogenetics, the Chromosomal Evolutionary Viewpoint, and Michael White's Signal Contributions to the Field". Journal of Orthoptera Research. 19 (2): 165–182. doi:10.1665/034.019.0202. hdl:11336/59292. S2CID 84319868.

harvard.edu

ui.adsabs.harvard.edu

Zhao, WW (May 1, 2015). "Robertsonian Translocations: An Overview of 872 Robertsonian Translocations Identified in a Diagnostic Laboratory in China". PLOS ONE. 10 (5): e0122647. Bibcode:2015PLoSO..1022647Z. doi:10.1371/journal.pone.0122647. PMC 4416705. PMID 25932913.

nih.gov

pubmed.ncbi.nlm.nih.gov

Nabors, R.K. (January 30, 1942). "Obituary: William Rees Brebner Robertson (1881-1941)". Science. 95 (2457): 113–114. doi:10.1126/science.95.2457.113. PMID 17795644.
Therman, E (February 1989). "The nonrandom participation of human afrocentric chromosomes in Robertsonian translocations". Annals of Human Genetics. 53 (53(Pt1)): 49–65. doi:10.1111/j.1469-1809.1989.tb01121.x. PMID 2658738. S2CID 1949436.
Zhao, WW (May 1, 2015). "Robertsonian Translocations: An Overview of 872 Robertsonian Translocations Identified in a Diagnostic Laboratory in China". PLOS ONE. 10 (5): e0122647. Bibcode:2015PLoSO..1022647Z. doi:10.1371/journal.pone.0122647. PMC 4416705. PMID 25932913.
Engels, Hartmut; Eggermann, Thomas; Caliebe, Almut; Jelska, Anna; Schubert, Regine; Schüler, Herdit M.; Panasiuk, Barbara; Zaremba, Jacek; Latos-BieleńSka, Anna; Jakubowski, Lucjusz; Zerres, Klaus P.; Schwanitz, Gesa; Midro, Alina T. (2008). "Genetic counseling in Robertsonian translocations der(13;14): Frequencies of reproductive outcomes and infertility in 101 pedigrees**". American Journal of Medical Genetics Part A. 146A (20): 2611–2616. doi:10.1002/ajmg.a.32500. PMID 18798317. S2CID 42829871.
RACHISAN AL; NICULAE AS; TINTEA I; POP B; MILITARU M; BIZO A; HRUSCA A (2017). "Association of fragile X syndrome, Robertsonian translocation (13, 22) and autism in a child". Clujul Medical. 90 (4): 445–448. doi:10.15386/cjmed-763. PMC 5683837. PMID 29151796.
Buoni, S.; Zannolli, R.; MacUcci, F.; Pucci, L.; Mogni, M.; Pierluigi, M.; Fois, A. (2006). "Familial robertsonian 13;14 translocation with mental retardation and epilepsy". Journal of Child Neurology. 21 (6): 531–3. doi:10.1177/08830738060210060701. PMID 16948942. S2CID 44812342.
Venkateshwari, A.; Srilekha, A.; Sunitha, T.; Pratibha, N.; Jyothy, A. (2010). "Robertsonian Translocation rob (14;15) (q10:q10) in a Patient with Recurrent Abortions: A Case Report". Journal of Reproduction & Infertility. 11 (3): 197–200. PMC 3719299. PMID 23926490.

ncbi.nlm.nih.gov

Zhao, WW (May 1, 2015). "Robertsonian Translocations: An Overview of 872 Robertsonian Translocations Identified in a Diagnostic Laboratory in China". PLOS ONE. 10 (5): e0122647. Bibcode:2015PLoSO..1022647Z. doi:10.1371/journal.pone.0122647. PMC 4416705. PMID 25932913.
RACHISAN AL; NICULAE AS; TINTEA I; POP B; MILITARU M; BIZO A; HRUSCA A (2017). "Association of fragile X syndrome, Robertsonian translocation (13, 22) and autism in a child". Clujul Medical. 90 (4): 445–448. doi:10.15386/cjmed-763. PMC 5683837. PMID 29151796.
Venkateshwari, A.; Srilekha, A.; Sunitha, T.; Pratibha, N.; Jyothy, A. (2010). "Robertsonian Translocation rob (14;15) (q10:q10) in a Patient with Recurrent Abortions: A Case Report". Journal of Reproduction & Infertility. 11 (3): 197–200. PMC 3719299. PMID 23926490.

semanticscholar.org

api.semanticscholar.org

Robertson, W.R.B. (1916). "Chromosome studies. I. Taxonomic relationships shown in the chromosomes of Tettigidae and Acrididae. V-shaped chromosomes and their significance in Acrididae, Locustidae and Gryllidae: chromosome and variation". Journal of Morphology. 27 (2): 179–331. doi:10.1002/jmor.1050270202. S2CID 86497936.
Therman, E (February 1989). "The nonrandom participation of human afrocentric chromosomes in Robertsonian translocations". Annals of Human Genetics. 53 (53(Pt1)): 49–65. doi:10.1111/j.1469-1809.1989.tb01121.x. PMID 2658738. S2CID 1949436.
Engels, Hartmut; Eggermann, Thomas; Caliebe, Almut; Jelska, Anna; Schubert, Regine; Schüler, Herdit M.; Panasiuk, Barbara; Zaremba, Jacek; Latos-BieleńSka, Anna; Jakubowski, Lucjusz; Zerres, Klaus P.; Schwanitz, Gesa; Midro, Alina T. (2008). "Genetic counseling in Robertsonian translocations der(13;14): Frequencies of reproductive outcomes and infertility in 101 pedigrees**". American Journal of Medical Genetics Part A. 146A (20): 2611–2616. doi:10.1002/ajmg.a.32500. PMID 18798317. S2CID 42829871.
Buoni, S.; Zannolli, R.; MacUcci, F.; Pucci, L.; Mogni, M.; Pierluigi, M.; Fois, A. (2006). "Familial robertsonian 13;14 translocation with mental retardation and epilepsy". Journal of Child Neurology. 21 (6): 531–3. doi:10.1177/08830738060210060701. PMID 16948942. S2CID 44812342.
Bidau, Claudio J.; Martí, Dardo A. (2010). "110 Years of Orthopteran Cytogenetics, the Chromosomal Evolutionary Viewpoint, and Michael White's Signal Contributions to the Field". Journal of Orthoptera Research. 19 (2): 165–182. doi:10.1665/034.019.0202. hdl:11336/59292. S2CID 84319868.

zenodo.org

Robertson, W.R.B. (1916). "Chromosome studies. I. Taxonomic relationships shown in the chromosomes of Tettigidae and Acrididae. V-shaped chromosomes and their significance in Acrididae, Locustidae and Gryllidae: chromosome and variation". Journal of Morphology. 27 (2): 179–331. doi:10.1002/jmor.1050270202. S2CID 86497936.