References analysis of the Wikipedia article "Prader-Villi sindromu" in the Azerbaijani version

books.google.com

Teitelbaum, Jonathan E. In a Page: Pediatrics (ingilis). Lippincott Williams & Wilkins. 2007. səh. 330. ISBN 9780781770453. 2017-09-11 tarixində arxivləşdirilib. İstifadə tarixi: 2021-06-30.

Mia, Md Mohan. Classical and Molecular Genetics (ingilis). American Academic Press. 2016. səh. 195. ISBN 978-1-63181-776-2. September 11, 2017 tarixində arxivləşdirilib.

Jorde, Lynn B.; Carey, John C.; Bamshad, Michael J. Medical Genetics (ingilis) (5). Elsevier Health Sciences. 2015. səh. 120. ISBN 978-0-323-18837-1. 2020-12-15 tarixində arxivləşdirilib. İstifadə tarixi: 2021-06-30.

Killeen, Anthony A. Genetic Inheritance // Principles of Molecular Pathology. Humana Press. 2004. səh. 41. ISBN 978-1-58829-085-4. June 29, 2014 tarixində arxivləşdirilib.

doi.org

Cortés M, F; Alliende R, MA; Barrios R, A; Curotto L, B; Santa María V, L; Barraza O, X; Troncoso A, L; Mellado S, C; Pardo V, R. "[Clinical, genetic and molecular features in 45 patients with Prader-Willi syndrome]". Revista Médica de Chile. 133 (1). January 2005: 33–41. doi:10.4067/s0034-98872005000100005. PMID 15768148.

Cassidy, Suzanne B; Driscoll, Daniel J. "Prader–Willi syndrome". European Journal of Human Genetics. 17 (1). September 10, 2008: 3–13. doi:10.1038/ejhg.2008.165. PMC 2985966. PMID 18781185.

Buiting, K; Saitoh, S; Gross, S; Dittrich, B; Schwartz, S; Nicholls, RD; Horsthemke, B. "Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15". Nature Genetics. 9 (4). April 1995: 395–400. doi:10.1038/ng0495-395. PMID 7795645.

de los Santos T, Schweizer J, Rees CA, Francke U. "Small evolutionarily conserved RNA, resembling C/D box small nucleolar RNA, is transcribed from PWCR1, a novel imprinted gene in the Prader-Willi deletion region, which is highly expressed in brain". American Journal of Human Genetics. 67 (5). November 2000: 1067–82. doi:10.1086/303106. PMC 1288549. PMID 11007541.

Whittington J, Holland A, Webb T, Butler J, Clarke D, Boer H. "Cognitive abilities and genotype in a population-based sample of people with Prader-Willi syndrome". J Intellect Disabil Res. 48 (Pt 2). February 2004: 172–87. doi:10.1111/j.1365-2788.2004.00556.x. PMID 14723659.

Cavaillé J, Buiting K, Kiefmann M, Lalande M, Brannan CI, Horsthemke B, Bachellerie JP, Brosius J, Hüttenhofer A. "Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization". Proc. Natl. Acad. Sci. U.S.A. 97 (26). December 2000: 14311–6. Bibcode:2000PNAS...9714311C. doi:10.1073/pnas.250426397. PMC 18915. PMID 11106375.

Boer, H; Holland, A; Whittington, J; Butler, J; Webb, T; Clarke, D. "Psychotic illness in people with Prader Willi syndrome due to chromosome 15 maternal uniparental disomy". Lancet. 359 (9301). January 12, 2002: 135–6. doi:10.1016/S0140-6736(02)07340-3. PMID 11809260.

Runte M, Varon R, Horn D, Horsthemke B, Buiting K. "Exclusion of the C/D box snoRNA gene cluster HBII-52 from a major role in Prader-Willi syndrome". Hum Genet. 116 (3). 2005: 228–30. doi:10.1007/s00439-004-1219-2. PMID 15565282.

Cassidy, SB; Dykens, E. "Prader-Willi and Angelman syndromes: sister imprinted disorders". Am J Med Genet. 97 (2). 2000: 136–146. doi:10.1002/1096-8628(200022)97:2<136::aid-ajmg5>3.0.co;2-v. PMID 11180221.

Skryabin BV, Gubar LV, Seeger B, Pfeiffer J, Handel S, Robeck T, Karpova E, Rozhdestvensky TS, Brosius J. "Deletion of the MBII-85 snoRNA gene cluster in mice results in postnatal growth retardation". PLOS Genet. 3 (12). 2007: e235. doi:10.1371/journal.pgen.0030235. PMC 2323313. PMID 18166085.

Sahoo T, del Gaudio D, German JR, Shinawi M, Peters SU, Person RE, Garnica A, Cheung SW, Beaudet AL. "Prader-Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA cluster". Nat Genet. 40 (6). 2008: 719–21. doi:10.1038/ng.158. PMC 2705197. PMID 18500341.

Ding F, Li HH, Zhang S, Solomon NM, Camper SA, Cohen P, Francke U. "SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice". PLOS ONE. 3 (3). March 2008: e1709. Bibcode:2008PLoSO...3.1709D. doi:10.1371/journal.pone.0001709. PMC 2248623. PMID 18320030.

Ding F, Prints Y, Dhar MS, Johnson DK, Garnacho-Montero C, Nicholls RD, Francke U. "Lack of Pwcr1/MBII-85 snoRNA is critical for neonatal lethality in Prader-Willi syndrome mouse models". Mamm Genome. 16 (6). 2005: 424–31. doi:10.1007/s00335-005-2460-2. PMID 16075369.

de Smith AJ, Purmann C, Walters RG, Ellis RJ, Holder SE, Van Haelst MM, Brady AF, Fairbrother UL, Dattani M, Keogh JM, Henning E, Yeo GS, O'Rahilly S, Froguel P, Farooqi IS, Blakemore AI. "A Deletion of the HBII-85 Class of Small Nucleolar RNAs (snoRNAs) is Associated with Hyperphagia, Obesity and Hypogonadism". Hum. Mol. Genet. 18 (17). June 2009: 3257–65. doi:10.1093/hmg/ddp263. PMC 2722987. PMID 19498035.

Carrel AL, Myers SE, Whitman BY, Allen DB. "Benefits of long-term GH therapy in Prader-Willi syndrome: a 4-year study". J. Clin. Endocrinol. Metab. 87 (4). April 2002: 1581–5. doi:10.1210/jc.87.4.1581. PMID 11932286.

Höybye C, Hilding A, Jacobsson H, Thorén M. "Growth hormone treatment improves body composition in adults with Prader-Willi syndrome". Clin. Endocrinol. 58 (5). May 2003: 653–61. doi:10.1046/j.1365-2265.2003.01769.x. PMID 12699450.

Scheimann, AO; Butler, MG; Gourash, L; Cuffari, C; Klish, W. "Critical analysis of bariatric procedures in Prader-Willi syndrome". Journal of Pediatric Gastroenterology and Nutrition. 46 (1). January 2008: 80–3. doi:10.1097/01.mpg.0000304458.30294.31. PMC 6815229. PMID 18162838.

nih.gov

ncbi.nlm.nih.gov

Cassidy, Suzanne B; Driscoll, Daniel J. "Prader–Willi syndrome". European Journal of Human Genetics. 17 (1). September 10, 2008: 3–13. doi:10.1038/ejhg.2008.165. PMC 2985966. PMID 18781185.

Holm, V. A.; Cassidy, S. B.; Butler, M. G.; Hanchett, J. M.; Greenswag, L. R.; Whitman, B. Y.; Greenberg, F. "Prader-Willi syndrome: consensus diagnostic criteria". Pediatrics. 91 (2). Feb 1993: 398–402. ISSN 0031-4005. PMC 6714046. PMID 8424017. 2022-08-08 tarixində arxivləşdirilib. İstifadə tarixi: 2021-06-30.

Curfs LM, Fryns JP. "Prader-Willi syndrome: a review with special attention to the cognitive and behavioral profile". Birth Defects Orig. Artic. Ser. 28 (1). 1992: 99–104. PMID 1340242.

Holm VA, Cassidy SB, Butler MG, Hanchett JM, Greenswag LR, Whitman BY, Greenberg F. "Prader-Willi syndrome: consensus diagnostic criteria". Pediatrics. 91 (2). 1993: 398–402. PMC 6714046. PMID 8424017.

"Prader-Willi Syndrome - MeSH - NCBI." National Center for Biotechnology Information. U.S. National Library of Medicine, n.d. Web. November 1, 2016. <"Prader-Willi Syndrome - MeSH - NCBI". November 3, 2016 tarixində arxivləşdirilib. İstifadə tarixi: November 1, 2016.>.

Hered RW, Rogers S, Zang YF, Biglan AW. "Ophthalmologic features of Prader-Willi syndrome". J Pediatr Ophthalmol Strabismus. 25 (3). 1988: 145–50. PMID 3397859.

nichd.nih.gov

ghr.nlm.nih.gov

"Angelman syndrome". Genetic Home Reference. May 2015. August 27, 2016 tarixində arxivləşdirilib. İstifadə tarixi: August 20, 2016.

"Prader-Willi syndrome". Genetics Home Reference. June 2014. August 27, 2016 tarixində arxivləşdirilib. İstifadə tarixi: August 19, 2016.

pubmed.ncbi.nlm.nih.gov

web.archive.org

Teitelbaum, Jonathan E. In a Page: Pediatrics (ingilis). Lippincott Williams & Wilkins. 2007. səh. 330. ISBN 9780781770453. 2017-09-11 tarixində arxivləşdirilib. İstifadə tarixi: 2021-06-30.

"Angelman syndrome". Genetic Home Reference. May 2015. August 27, 2016 tarixində arxivləşdirilib. İstifadə tarixi: August 20, 2016.

"Is there a cure for Prader-Willi syndrome (PWS)?". NICHD. January 14, 2014. August 27, 2016 tarixində arxivləşdirilib. İstifadə tarixi: August 20, 2016.

"What are the treatments for Prader-Willi syndrome (PWS)?". NICHD. January 14, 2014. August 10, 2016 tarixində arxivləşdirilib. İstifadə tarixi: August 20, 2016.

"Prader-Willi syndrome". Genetics Home Reference. June 2014. August 27, 2016 tarixində arxivləşdirilib. İstifadə tarixi: August 19, 2016.

"Prader-Labhardt-Willi syndrome". Whonamedit?. August 21, 2016 tarixində arxivləşdirilib. İstifadə tarixi: August 20, 2016.

Mia, Md Mohan. Classical and Molecular Genetics (ingilis). American Academic Press. 2016. səh. 195. ISBN 978-1-63181-776-2. September 11, 2017 tarixində arxivləşdirilib.

"Mayo Clinic, Diseases and Conditions". Prader-Willi Syndrome, Symptoms and Causes. 16 December 2018 tarixində arxivləşdirilib. İstifadə tarixi: 6 February 2019.

"Major breakthrough in understanding Prader-Willi syndrome, a parental imprinting disorder". Medicalxpress.com. April 28, 2015 tarixində arxivləşdirilib. İstifadə tarixi: June 18, 2015.

Udwin O. "Prader-Willi syndrome: Psychological and behavioural characteristics". Contact a Family. November 1998. July 16, 2011 tarixində orijinalından arxivləşdirilib.

"What are the treatments for Prader-Willi syndrome (PWS)?". July 6, 2016 tarixində arxivləşdirilib. İstifadə tarixi: June 16, 2016.

Killeen, Anthony A. Genetic Inheritance // Principles of Molecular Pathology. Humana Press. 2004. səh. 41. ISBN 978-1-58829-085-4. June 29, 2014 tarixində arxivləşdirilib.

Tweed, Katherine. "Shawn Cooper Struggles with Prader Willi Syndrome". AOL Health. sentyabr 2009. sentyabr 9, 2009 tarixində arxivləşdirilib. İstifadə tarixi: sentyabr 9, 2009.

[1] Arxiv surəti 14 iyul 2014 tarixindən Wayback Machine saytında Arxivləşdirilib iyul 14, 2014, at the Wayback Machine

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Prader-Villi sindromu (Azerbaijani Wikipedia)

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cafamily.org.uk

disease-ontology.org

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ui.adsabs.harvard.edu

mayoclinic.org

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