片親性ダイソミー (Japanese Wikipedia)

Analysis of information sources in references of the Wikipedia article "片親性ダイソミー" in Japanese language version.

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archive.org

Human Molecular Genetics 3. Garland Science. pp. 58. ISBN 0-8153-4183-0

archive.today

Bhatt, Arpan; Liehr, Thomas; Bakshi, Sonal R. (2013). “Phenotypic spectrum in uniparental disomy: Low incidence or lack of study”. Indian Journal of Human Genetics 19 (3): 131–34. doi:10.4103/0971-6866.120819. PMC 3841555. PMID 24339543. オリジナルの2014-02-20時点におけるアーカイブ。.

diseasesdatabase.com

“Chromosome 14 uniparental disomy syndrome information Diseases Database” (英語). www.diseasesdatabase.com (2020年9月1日). 2020年9月1日閲覧。

doi.org

Robinson WP (May 2000). “Mechanisms leading to uniparental disomy and their clinical consequences”. BioEssays 22 (5): 452–9. doi:10.1002/(SICI)1521-1878(200005)22:5<452::AID-BIES7>3.0.CO;2-K. PMID 10797485.
King DA (2013). “A novel method for detecting uniparental disomy from trio genotypes identifies a significant excess in children with developmental disorders”. Genome Research 24 (4): 673–687. doi:10.1101/gr.160465.113. PMC 3975066. PMID 24356988.
Nakka, Priyanka; Smith, Samuel Pattillo; O’Donnell-Luria, Anne H.; McManus, Kimberly F.; Agee, Michelle; Auton, Adam; Bell, Robert K.; Bryc, Katarzyna et al. (2019-11-07). “Characterization of Prevalence and Health Consequences of Uniparental Disomy in Four Million Individuals from the General Population” (英語). The American Journal of Human Genetics 105 (5): 921–932. doi:10.1016/j.ajhg.2019.09.016. ISSN 0002-9297. PMC 6848996. PMID 31607426.
Bhatt, Arpan; Liehr, Thomas; Bakshi, Sonal R. (2013). “Phenotypic spectrum in uniparental disomy: Low incidence or lack of study”. Indian Journal of Human Genetics 19 (3): 131–34. doi:10.4103/0971-6866.120819. PMC 3841555. PMID 24339543. オリジナルの2014-02-20時点におけるアーカイブ。.
Bens, Susanne; Luedeke, Manuel; Richter, Tanja; Graf, Melanie; Kolarova, Julia; Barbi, Gotthold; Lato, Krisztian; Barth, Thomas F. et al. (2017). “Mosaic genome-wide maternal isodiploidy: an extreme form of imprinting disorder presenting as prenatal diagnostic challenge”. Clinical Epigenetics 9: 111. doi:10.1186/s13148-017-0410-y. ISSN 1868-7083. PMC 5640928. PMID 29046733.

ijhg.com

Bhatt, Arpan; Liehr, Thomas; Bakshi, Sonal R. (2013). “Phenotypic spectrum in uniparental disomy: Low incidence or lack of study”. Indian Journal of Human Genetics 19 (3): 131–34. doi:10.4103/0971-6866.120819. PMC 3841555. PMID 24339543. オリジナルの2014-02-20時点におけるアーカイブ。.

nih.gov

pubmed.ncbi.nlm.nih.gov

Robinson WP (May 2000). “Mechanisms leading to uniparental disomy and their clinical consequences”. BioEssays 22 (5): 452–9. doi:10.1002/(SICI)1521-1878(200005)22:5<452::AID-BIES7>3.0.CO;2-K. PMID 10797485.
King DA (2013). “A novel method for detecting uniparental disomy from trio genotypes identifies a significant excess in children with developmental disorders”. Genome Research 24 (4): 673–687. doi:10.1101/gr.160465.113. PMC 3975066. PMID 24356988.
Nakka, Priyanka; Smith, Samuel Pattillo; O’Donnell-Luria, Anne H.; McManus, Kimberly F.; Agee, Michelle; Auton, Adam; Bell, Robert K.; Bryc, Katarzyna et al. (2019-11-07). “Characterization of Prevalence and Health Consequences of Uniparental Disomy in Four Million Individuals from the General Population” (英語). The American Journal of Human Genetics 105 (5): 921–932. doi:10.1016/j.ajhg.2019.09.016. ISSN 0002-9297. PMC 6848996. PMID 31607426.
Bhatt, Arpan; Liehr, Thomas; Bakshi, Sonal R. (2013). “Phenotypic spectrum in uniparental disomy: Low incidence or lack of study”. Indian Journal of Human Genetics 19 (3): 131–34. doi:10.4103/0971-6866.120819. PMC 3841555. PMID 24339543. オリジナルの2014-02-20時点におけるアーカイブ。.
Bens, Susanne; Luedeke, Manuel; Richter, Tanja; Graf, Melanie; Kolarova, Julia; Barbi, Gotthold; Lato, Krisztian; Barth, Thomas F. et al. (2017). “Mosaic genome-wide maternal isodiploidy: an extreme form of imprinting disorder presenting as prenatal diagnostic challenge”. Clinical Epigenetics 9: 111. doi:10.1186/s13148-017-0410-y. ISSN 1868-7083. PMC 5640928. PMID 29046733.
“Uniparental disomy as a mechanism for human genetic disease”. American Journal of Human Genetics 42 (2): 217–226. (1988). PMC 1715272. PMID 2893543.

pmc.ncbi.nlm.nih.gov

King DA (2013). “A novel method for detecting uniparental disomy from trio genotypes identifies a significant excess in children with developmental disorders”. Genome Research 24 (4): 673–687. doi:10.1101/gr.160465.113. PMC 3975066. PMID 24356988.
Nakka, Priyanka; Smith, Samuel Pattillo; O’Donnell-Luria, Anne H.; McManus, Kimberly F.; Agee, Michelle; Auton, Adam; Bell, Robert K.; Bryc, Katarzyna et al. (2019-11-07). “Characterization of Prevalence and Health Consequences of Uniparental Disomy in Four Million Individuals from the General Population” (英語). The American Journal of Human Genetics 105 (5): 921–932. doi:10.1016/j.ajhg.2019.09.016. ISSN 0002-9297. PMC 6848996. PMID 31607426.
Bhatt, Arpan; Liehr, Thomas; Bakshi, Sonal R. (2013). “Phenotypic spectrum in uniparental disomy: Low incidence or lack of study”. Indian Journal of Human Genetics 19 (3): 131–34. doi:10.4103/0971-6866.120819. PMC 3841555. PMID 24339543. オリジナルの2014-02-20時点におけるアーカイブ。.
Bens, Susanne; Luedeke, Manuel; Richter, Tanja; Graf, Melanie; Kolarova, Julia; Barbi, Gotthold; Lato, Krisztian; Barth, Thomas F. et al. (2017). “Mosaic genome-wide maternal isodiploidy: an extreme form of imprinting disorder presenting as prenatal diagnostic challenge”. Clinical Epigenetics 9: 111. doi:10.1186/s13148-017-0410-y. ISSN 1868-7083. PMC 5640928. PMID 29046733.
“Uniparental disomy as a mechanism for human genetic disease”. American Journal of Human Genetics 42 (2): 217–226. (1988). PMC 1715272. PMID 2893543.

ncbi.nlm.nih.gov

King DA (2013). “A novel method for detecting uniparental disomy from trio genotypes identifies a significant excess in children with developmental disorders”. Genome Research 24 (4): 673–687. doi:10.1101/gr.160465.113. PMC 3975066. PMID 24356988.
Nakka, Priyanka; Smith, Samuel Pattillo; O’Donnell-Luria, Anne H.; McManus, Kimberly F.; Agee, Michelle; Auton, Adam; Bell, Robert K.; Bryc, Katarzyna et al. (2019-11-07). “Characterization of Prevalence and Health Consequences of Uniparental Disomy in Four Million Individuals from the General Population” (英語). The American Journal of Human Genetics 105 (5): 921–932. doi:10.1016/j.ajhg.2019.09.016. ISSN 0002-9297. PMC 6848996. PMID 31607426.
“Uniparental disomy as a mechanism for human genetic disease”. American Journal of Human Genetics 42 (2): 217–226. (1988). PMC 1715272. PMID 2893543.

omim.org

“OMIM Entry - # 608149 - KAGAMI-OGATA SYNDROME” (英語). omim.org. 2020年9月1日閲覧。

ufl.edu

peds.ufl.edu

“Meiosis: Uniparental Disomy”. 2016年2月29日閲覧。

web.archive.org

“OMIM Entry - # 105830 - ANGELMAN SYNDROME; AS”. web.archive.org (2014年5月29日). 2022年7月10日閲覧。

worldcat.org

search.worldcat.org

Nakka, Priyanka; Smith, Samuel Pattillo; O’Donnell-Luria, Anne H.; McManus, Kimberly F.; Agee, Michelle; Auton, Adam; Bell, Robert K.; Bryc, Katarzyna et al. (2019-11-07). “Characterization of Prevalence and Health Consequences of Uniparental Disomy in Four Million Individuals from the General Population” (英語). The American Journal of Human Genetics 105 (5): 921–932. doi:10.1016/j.ajhg.2019.09.016. ISSN 0002-9297. PMC 6848996. PMID 31607426.
Bens, Susanne; Luedeke, Manuel; Richter, Tanja; Graf, Melanie; Kolarova, Julia; Barbi, Gotthold; Lato, Krisztian; Barth, Thomas F. et al. (2017). “Mosaic genome-wide maternal isodiploidy: an extreme form of imprinting disorder presenting as prenatal diagnostic challenge”. Clinical Epigenetics 9: 111. doi:10.1186/s13148-017-0410-y. ISSN 1868-7083. PMC 5640928. PMID 29046733.