13q deletion syndrome (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "13q deletion syndrome" in English language version.

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doi.org

Wang, Y. P.; Wang, D. J.; Niu, Z. B.; Cui, W. T. (2017). "Chromosome 13q deletion syndrome involving 13q31-qter: A case report". Molecular Medicine Reports. 15 (6): 3658–3664. doi:10.3892/mmr.2017.6425. PMC 5436299. PMID 28393221.
Rapini, Novella; Lidano, Roberta (2014). "De Novo 13q13.3-21.31 deletion involving RB1 gene in a patient with hemangioendothelioma of the liver". Italian Journal of Pediatrics. 40 (4): 5. doi:10.1186/1824-7288-40-5. PMC 3896849. PMID 24433316.

medicinenet.com

"Medical Definition Of Long Arm Of A Chromosome". www.medicinenet.com/script/main/hp.asp. Archived from the original on 2020-06-21. Retrieved 2019-11-28.

nih.gov

pubmed.ncbi.nlm.nih.gov

Wang, Y. P.; Wang, D. J.; Niu, Z. B.; Cui, W. T. (2017). "Chromosome 13q deletion syndrome involving 13q31-qter: A case report". Molecular Medicine Reports. 15 (6): 3658–3664. doi:10.3892/mmr.2017.6425. PMC 5436299. PMID 28393221.
Manolakos, E.; Peitsidis, P.; Garas, A.; Vetro, A.; Eleftheriades, M.; Petersen, M. B.; Papoulidis, I. (2012-01-01). "First trimester diagnosis of 13q-syndrome associated with increased fetal nuchal translucency thickness. Clinical findings and systematic review". Clinical and Experimental Obstetrics & Gynecology. 39 (1): 118–121. ISSN 0390-6663. PMID 22675970.
Rapini, Novella; Lidano, Roberta (2014). "De Novo 13q13.3-21.31 deletion involving RB1 gene in a patient with hemangioendothelioma of the liver". Italian Journal of Pediatrics. 40 (4): 5. doi:10.1186/1824-7288-40-5. PMC 3896849. PMID 24433316.

ncbi.nlm.nih.gov

Wang, Y. P.; Wang, D. J.; Niu, Z. B.; Cui, W. T. (2017). "Chromosome 13q deletion syndrome involving 13q31-qter: A case report". Molecular Medicine Reports. 15 (6): 3658–3664. doi:10.3892/mmr.2017.6425. PMC 5436299. PMID 28393221.
Rapini, Novella; Lidano, Roberta (2014). "De Novo 13q13.3-21.31 deletion involving RB1 gene in a patient with hemangioendothelioma of the liver". Italian Journal of Pediatrics. 40 (4): 5. doi:10.1186/1824-7288-40-5. PMC 3896849. PMID 24433316.

omim.org

"OMIM Entry - # 613884 - CHROMOSOME 13q14 DELETION SYNDROME". www.omim.org. Retrieved 2019-10-08.

rarediseases.org

"Chromosome 13, Partial Monosomy 13q". www.rarediseases.org. Retrieved 2015-07-22.

socialstyrelsen.se

"13q deletion syndrome". www.socialstyrelsen.se. Archived from the original on 2019-04-08. Retrieved 2019-11-28.

web.archive.org

"13q deletion syndrome". www.socialstyrelsen.se. Archived from the original on 2019-04-08. Retrieved 2019-11-28.
"Medical Definition Of Long Arm Of A Chromosome". www.medicinenet.com/script/main/hp.asp. Archived from the original on 2020-06-21. Retrieved 2019-11-28.

worldcat.org

search.worldcat.org

Manolakos, E.; Peitsidis, P.; Garas, A.; Vetro, A.; Eleftheriades, M.; Petersen, M. B.; Papoulidis, I. (2012-01-01). "First trimester diagnosis of 13q-syndrome associated with increased fetal nuchal translucency thickness. Clinical findings and systematic review". Clinical and Experimental Obstetrics & Gynecology. 39 (1): 118–121. ISSN 0390-6663. PMID 22675970.