Cromosoma 15 (Galician Wikipedia)

Analysis of information sources in references of the Wikipedia article "Cromosoma 15" in Galician language version.

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13nih.gov

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books.google.com

Tom Strachan; Andrew Read (2 April 2010). Human Molecular Genetics. Garland Science. p. 45. ISBN 978-1-136-84407-2.

doi.org

dx.doi.org

Gilbert F (1999). "Disease genes and chromosomes: disease maps of the human genome. Chromosome 15". Genet Test 3 (3): 309–322. PMID 10495933. doi:10.1089/109065799316653. PMID 10495933
Lee S, Wevrick R (2000). "Identification of novel imprinted transcripts in the Prader-Willi syndrome and Angelman syndrome deletion region: further evidence for regional imprinting control". Am J Hum Genet 66 (3): 848–858. PMC 1288168. PMID 10712201. doi:10.1086/302817. PMID 10712201
Clayton-Smith J, Laan L (2003). "Angelman syndrome: a review of the clinical and genetic aspects". J Med Genet 40 (2): 87–95. PMC 1735357. PMID 12566516. doi:10.1136/jmg.40.2.87. PMID 12566516
Bittel DC, Kibiryeva N, Talebizadeh Z, Driscoll DJ, Butler MG (2005). "Microarray analysis of gene/transcript expression in Angelman syndrome: deletion versus UPD". Genomics 85 (1): 85–91. PMID 15607424. doi:10.1016/j.ygeno.2004.10.010. PMID 15607424
Bittel DC, Butler MG (2005). "Prader-Willi syndrome: clinical genetics, cytogenetics and molecular biology". Expert Rev Mol Med 7 (14): 1–20. PMID 16038620. doi:10.1017/S1462399405009531. PMID 16038620
Bittel DC, Kibiryeva N, Talebizadeh Z, Butler MG (2003). "Microarray analysis of gene/transcript expression in Prader-Willi syndrome: deletion versus UPD". J Med Genet 40 (8): 568–574. PMC 1735542. PMID 12920063. doi:10.1136/jmg.40.8.568. PMID 12920063
Butler MG, Bittel DC, Kibiryeva N, Talebizadeh Z, Thompson T (2004). "Behavioral differences among subjects with Prader-Willi syndrome and type I or type II deletion and maternal disomy". Pediatrics 113 (3 Pt 1): 565–573. PMID 14993551. doi:10.1542/peds.113.3.565. PMID 14993551
Borgatti R, Piccinelli P, Passoni D, Dalpra L, Miozzo M, Micheli R, Gagliardi C, Balottin U (2001). "Relationship between clinical and genetic features in "inverted duplicated chromosome 15" patients". Pediatr Neurol 24 (2): 111–116. PMID 11275459. doi:10.1016/S0887-8994(00)00244-7. PMID 11275459

nih.gov

ncbi.nlm.nih.gov

"Human Genome Assembly GRCh38 – Genome Reference Consortium". National Center for Biotechnology Information (en inglés). 2013-12-24. Consultado o 2017-03-04.
"Search results – 15[CHR] AND "Homo sapiens"[Organism] AND ("has ccds"[Properties] AND alive[prop]) – Gene". NCBI. CCDS Release 20 for Homo sapiens. 2016-09-08. Consultado o 2017-05-28.
Gilbert F (1999). "Disease genes and chromosomes: disease maps of the human genome. Chromosome 15". Genet Test 3 (3): 309–322. PMID 10495933. doi:10.1089/109065799316653. PMID 10495933
Cassidy SB, Dykens E, Williams CA (2000). "Prader-Willi and Angelman syndromes: sister imprinted disorders". Am J Med Genet 97 (2): 136–146. PMID 11180221. PMID 11180221
Lee S, Wevrick R (2000). "Identification of novel imprinted transcripts in the Prader-Willi syndrome and Angelman syndrome deletion region: further evidence for regional imprinting control". Am J Hum Genet 66 (3): 848–858. PMC 1288168. PMID 10712201. doi:10.1086/302817. PMID 10712201
Clayton-Smith J, Laan L (2003). "Angelman syndrome: a review of the clinical and genetic aspects". J Med Genet 40 (2): 87–95. PMC 1735357. PMID 12566516. doi:10.1136/jmg.40.2.87. PMID 12566516
Bittel DC, Kibiryeva N, Talebizadeh Z, Driscoll DJ, Butler MG (2005). "Microarray analysis of gene/transcript expression in Angelman syndrome: deletion versus UPD". Genomics 85 (1): 85–91. PMID 15607424. doi:10.1016/j.ygeno.2004.10.010. PMID 15607424
Bittel DC, Butler MG (2005). "Prader-Willi syndrome: clinical genetics, cytogenetics and molecular biology". Expert Rev Mol Med 7 (14): 1–20. PMID 16038620. doi:10.1017/S1462399405009531. PMID 16038620
Bittel DC, Kibiryeva N, Talebizadeh Z, Butler MG (2003). "Microarray analysis of gene/transcript expression in Prader-Willi syndrome: deletion versus UPD". J Med Genet 40 (8): 568–574. PMC 1735542. PMID 12920063. doi:10.1136/jmg.40.8.568. PMID 12920063
Butler MG, Bittel DC, Kibiryeva N, Talebizadeh Z, Thompson T (2004). "Behavioral differences among subjects with Prader-Willi syndrome and type I or type II deletion and maternal disomy". Pediatrics 113 (3 Pt 1): 565–573. PMID 14993551. doi:10.1542/peds.113.3.565. PMID 14993551
Borgatti R, Piccinelli P, Passoni D, Dalpra L, Miozzo M, Micheli R, Gagliardi C, Balottin U (2001). "Relationship between clinical and genetic features in "inverted duplicated chromosome 15" patients". Pediatr Neurol 24 (2): 111–116. PMID 11275459. doi:10.1016/S0887-8994(00)00244-7. PMID 11275459
Rineer S, Finucane B, Simon EW (1998). "Autistic symptoms among children and young adults with isodicentric chromosome 15". Am J Med Genet 81 (5): 428–433. PMID 9754629. PMID 9754629
Zollino M, Tiziano F, Di Stefano C, Neri G (1999). "Partial duplication of the long arm of chromosome 15: confirmation of a causative role in craniosynostosis and definition of a 15q25-qter trisomy syndrome". Am J Med Genet 87 (5): 391–394. PMID 10594876. PMID 10594876 [1]

pbs.org

"Teacher's Guide". Ghost in Your Genes (season 35). Nova (TV series). October 16, 2007. Consultado o 2009-09-26. O programa...conta como un científico determinou como a deleción dunha secuencia chave do ADN no cromosoma humano 15 podía orixinar dúas síndromes diferentes dependendo de se a deleción se orixinaba na nai ou no pai [e] explica que isto era a primeira evidencia de que algo ademais dos xenes podía determinar como se expresan os xenes.