Cromosoma 8 (humano) (Spanish Wikipedia)

Analysis of information sources in references of the Wikipedia article "Cromosoma 8 (humano)" in Spanish language version.

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doi.org

dx.doi.org

Blouin JL, Dombroski BA, Nath SK, et al (septiembre de 1998). «Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21». Nat. Genet. 20 (1): 70-3. PMID 9731535. doi:10.1038/1734.
Gurling HM, Kalsi G, Brynjolfson J, et al (marzo de 2001). «Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23». Am. J. Hum. Genet. 68 (3): 661-73. PMC 1274479. PMID 11179014. doi:10.1086/318788.
Suarez BK, Duan J, Sanders AR, et al (febrero de 2006). «Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia: suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sample». Am. J. Hum. Genet. 78 (2): 315-33. PMC 1380238. PMID 16400611. doi:10.1086/500272.

elsevier.com

linkinghub.elsevier.com

Gurling HM, Kalsi G, Brynjolfson J, et al (marzo de 2001). «Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23». Am. J. Hum. Genet. 68 (3): 661-73. PMC 1274479. PMID 11179014. doi:10.1086/318788.
Suarez BK, Duan J, Sanders AR, et al (febrero de 2006). «Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia: suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sample». Am. J. Hum. Genet. 78 (2): 315-33. PMC 1380238. PMID 16400611. doi:10.1086/500272.

emedicine.com

Poiquilodermia congénita

nih.gov

ncbi.nlm.nih.gov

Blouin JL, Dombroski BA, Nath SK, et al (septiembre de 1998). «Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21». Nat. Genet. 20 (1): 70-3. PMID 9731535. doi:10.1038/1734.
Gurling HM, Kalsi G, Brynjolfson J, et al (marzo de 2001). «Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23». Am. J. Hum. Genet. 68 (3): 661-73. PMC 1274479. PMID 11179014. doi:10.1086/318788.
Suarez BK, Duan J, Sanders AR, et al (febrero de 2006). «Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia: suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sample». Am. J. Hum. Genet. 78 (2): 315-33. PMC 1380238. PMID 16400611. doi:10.1086/500272.
M. Mantegazza et al.: Identification of an Nav1.1 sodium channel (SCN1A) loss-of-function mutation associated with familial simple febrile seizures (artículo completo disponible en inglés). Proc Natl Acad Sc USA. 2005; 102:18177-18182 PMID 16326807

pubmedcentral.nih.gov

M. Mantegazza et al.: Identification of an Nav1.1 sodium channel (SCN1A) loss-of-function mutation associated with familial simple febrile seizures (artículo completo disponible en inglés). Proc Natl Acad Sc USA. 2005; 102:18177-18182 PMID 16326807