单亲二体 (Chinese Wikipedia)

Analysis of information sources in references of the Wikipedia article "单亲二体" in Chinese language version.

refsWebsite

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20doi.org

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15web.archive.org

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13worldcat.org

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10nih.gov

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6wiley.com

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2sciencedirect.com

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2elsevier.com

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1sciengine.com

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1yiigle.com

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8,430^th place

1biomedcentral.com

2,747^th place

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biomedcentral.com

molecularcytogenetics.biomedcentral.com

Chantot-Bastaraud, Sandra; Stratmann, Svea; Brioude, Frédéric; Begemann, Matthias; Elbracht, Miriam; Graul-Neumann, Luitgard; Harbison, Madeleine; Netchine, Irène; Eggermann, Thomas. Formation of upd(7)mat by trisomic rescue: SNP array typing provides new insights in chromosomal nondisjunction. Molecular Cytogenetics. 2017-12, 10 (1) [2024-01-19]. ISSN 1755-8166. PMC 5526280 . PMID 28770003. doi:10.1186/s13039-017-0329-1. （原始内容存档于2023-02-25）（英语）.

doi.org

Benn, Peter. Uniparental disomy: Origin, frequency, and clinical significance. Prenatal Diagnosis. 2021-04, 41 (5) [2024-01-23]. ISSN 0197-3851. doi:10.1002/pd.5837. （原始内容存档于2024-01-08）（英语）.
单亲二体及其在癌症中的作用研究进展. www.sciengine.com. [2024-01-16]. PMC 8800777 . PMID 31901032. doi:10.3785/j.issn.1008-9292.2019.10.15. （原始内容存档于2024-01-05）（中文）. Uniparental disomy (UPD) refers to a chromosome defect that an individual's homologous chromosome or segments are inherited from one parent.
Shaffer, Lisa G; Agan, Noelle; Goldberg, James D; Ledbetter, David H; Longshore, John W; Cassidy, Suzanne B. American College of Medical Genetics Statement on Diagnostic Testing for Uniparental Disomy. Genetics in Medicine. 2001-05, 3 (3). ISSN 1098-3600. PMC 3111049 . PMID 11388763. doi:10.1097/00125817-200105000-00011.
Engel, Eric. A new genetic concept: Uniparental disomy and its potential effect, isodisomy. American Journal of Medical Genetics. 1980-01, 6 (2) [2024-02-02]. ISSN 0148-7299. doi:10.1002/ajmg.1320060207. （原始内容存档于2024-02-02）（英语）.
崔婉婷赵彦艳. 染色体嵌合体及单亲二体的研究现状 Current research status on chromosomal mosaicism and uniparental disomy. 中华妇幼临床医学杂志(电子版). 2022 -04 -01 [2024-04-02]. doi:10.3877/cma.j.issn.1673-5250.2022.02.002. （原始内容存档于2024-04-03） –通过中华医学期刊全文数据库（中文）. 单亲二体(uniparental disomy，UPD)是指某一同源染色体均遗传自双亲之一请检查|date=中的日期值 (帮助)
Robinson, Wendy P. Mechanisms leading to uniparental disomy and their clinical consequences. BioEssays. 2000-04-24, 22 (5). doi:10.1002/(SICI)1521-1878(200005)22:5<452::AID-BIES7>3.0.CO;2-K （英语）. Uniparental disomy (UPD) refers to the situation in which both copies of a chromosome pair have originated from one parent.
Yamazawa, Kazuki; Ogata, Tsutomu; Ferguson‐Smith, Anne C. Uniparental disomy and human disease: An overview. American Journal of Medical Genetics Part C: Seminars in Medical Genetics. 2010-08-15, 154C (3) [2024-03-06]. ISSN 1552-4868. doi:10.1002/ajmg.c.30270. （原始内容存档于2024-04-30）（英语）.
贾静; 何梦舟; 张婧怡; 陈凯月; 唐红菊; 冯玲. 单亲二倍体染色体异常的研究进展. 国际生殖健康/计划生育杂志. 2017-09, 36 (5): 408-411. doi:10.3969/j.issn.1674-1889.2017.05.015 –通过SinoMed.
Cook, Jackie. 7 - Genes in Families. Pyeritz, Reed E. (编). Emery and Rimoin's Principles and Practice of Medical Genetics and Genomics (Seventh Edition). Academic Press. 2019-01-01: 201–225 [2024-01-16]. ISBN 978-0-12-812537-3. doi:10.1016/b978-0-12-812537-3.00007-x. （原始内容存档于2022-04-03）.
Xin, Yalan; Fang, Hui; Yuan, Penghui; Jiang, Yushen. [Genetic analysis of an adult with mosaicism of uniparental disomy 11p]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 2019-12-10, 36 (12) [2024-01-16]. ISSN 1003-9406. PMID 31813152. doi:10.3760/cma.j.issn.1003-9406.2019.12.017. （原始内容存档于2024-01-16）.
Eggermann, Thomas; Soellner, Lukas; Buiting, Karin; Kotzot, Dieter. Mosaicism and uniparental disomy in prenatal diagnosis. Trends in Molecular Medicine. 2015-02, 21 (2) [2024-01-23]. ISSN 1471-4914. doi:10.1016/j.molmed.2014.11.010. （原始内容存档于2024-01-23）.
Créau-Goldberg, Nicole; Gegonne, Anne; Delabar, Jean; Cochet, Chantal; Cabanis, Marie-Odile; Stehelin, Dominique; Turleau, Catherine; de Grouchy, Jean. Maternal origin of a de novo balanced t(21q21q) identified by ets-2 polymorphism. Human Genetics. 1987-08-01, 76 (4). ISSN 1432-1203. doi:10.1007/BF00272452 （英语）.
Wang, Y.; Li, Y.; Chen, Y.; Zhou, R.; Sang, Z.; Meng, L.; Tan, J.; Qiao, F.; Bao, Q.; Luo, D.; Peng, C. Systematic analysis of copy‐number variations associated with early pregnancy loss. Ultrasound in Obstetrics & Gynecology. 2020-01, 55 (1) [2024-02-02]. ISSN 0960-7692. doi:10.1002/uog.20412. （原始内容存档于2024-02-02）（英语）.
Trent, Ronald J. 4 - COMPLEX GENETIC TRAITS. Trent, Ronald J (编). Molecular Medicine (Third Edition). Burlington: Academic Press. 2005-01-01: 77–118 [2024-01-16]. ISBN 978-0-12-699057-7. doi:10.1016/b978-012699057-7/50004-7. （原始内容存档于2022-04-03）.
Chantot-Bastaraud, Sandra; Stratmann, Svea; Brioude, Frédéric; Begemann, Matthias; Elbracht, Miriam; Graul-Neumann, Luitgard; Harbison, Madeleine; Netchine, Irène; Eggermann, Thomas. Formation of upd(7)mat by trisomic rescue: SNP array typing provides new insights in chromosomal nondisjunction. Molecular Cytogenetics. 2017-12, 10 (1) [2024-01-19]. ISSN 1755-8166. PMC 5526280 . PMID 28770003. doi:10.1186/s13039-017-0329-1. （原始内容存档于2023-02-25）（英语）.
Shaffer, Lisa G; Agan, Noelle; Goldberg, James D; Ledbetter, David H; Longshore, John W; Cassidy, Suzanne B. American College of Medical Genetics Statement on Diagnostic Testing for Uniparental Disomy. Genetics in Medicine. 2001-05, 3 (3) [2024-01-17]. PMC 3111049 . PMID 11388763. doi:10.1097/00125817-200105000-00011. （原始内容存档于2023-11-18）（英语）.
Hoppman, Nicole; Rumilla, Kandelaria; Lauer, Emily; Kearney, Hutton; Thorland, Erik. Patterns of homozygosity in patients with uniparental disomy: detection rate and suggested reporting thresholds for SNP microarrays. Genetics in Medicine. 2018-12, 20 (12). ISSN 1098-3600. doi:10.1038/gim.2018.24.
Bis, Dana M.; Schüle, Rebecca; Reichbauer, Jennifer; Synofzik, Matthis; Rattay, Tim W.; Soehn, Anne; de Jonghe, Peter; Schöls, Ludger; Züchner, Stephan. Uniparental disomy determined by whole‐exome sequencing in a spectrum of rare motoneuron diseases and ataxias. Molecular Genetics & Genomic Medicine. 2017-05, 5 (3) [2024-01-28]. ISSN 2324-9269. PMC 5441426 . PMID 28546998. doi:10.1002/mgg3.285. （原始内容存档于2024-01-28）（英语）.
Yauy, Kevin; de Leeuw, Nicole; Yntema, Helger G.; Pfundt, Rolph; Gilissen, Christian. Accurate detection of clinically relevant uniparental disomy from exome sequencing data. Genetics in Medicine. 2020-04, 22 (4) [2024-01-28]. PMC 7118024 . PMID 31767986. doi:10.1038/s41436-019-0704-x. （原始内容存档于2024-04-12）（英语）.
Zlotogora, Joel. Parents of children with autosomal recessive diseases are not always carriers of the respective mutant alleles. Human Genetics. 2004-05-01, 114 (6). ISSN 1432-1203. doi:10.1007/s00439-004-1105-y （英语）.

elsevier.com

linkinghub.elsevier.com

Shaffer, Lisa G; Agan, Noelle; Goldberg, James D; Ledbetter, David H; Longshore, John W; Cassidy, Suzanne B. American College of Medical Genetics Statement on Diagnostic Testing for Uniparental Disomy. Genetics in Medicine. 2001-05, 3 (3) [2024-01-17]. PMC 3111049 . PMID 11388763. doi:10.1097/00125817-200105000-00011. （原始内容存档于2023-11-18）（英语）.
Yauy, Kevin; de Leeuw, Nicole; Yntema, Helger G.; Pfundt, Rolph; Gilissen, Christian. Accurate detection of clinically relevant uniparental disomy from exome sequencing data. Genetics in Medicine. 2020-04, 22 (4) [2024-01-28]. PMC 7118024 . PMID 31767986. doi:10.1038/s41436-019-0704-x. （原始内容存档于2024-04-12）（英语）.

nih.gov

ncbi.nlm.nih.gov

单亲二体及其在癌症中的作用研究进展. www.sciengine.com. [2024-01-16]. PMC 8800777 . PMID 31901032. doi:10.3785/j.issn.1008-9292.2019.10.15. （原始内容存档于2024-01-05）（中文）. Uniparental disomy (UPD) refers to a chromosome defect that an individual's homologous chromosome or segments are inherited from one parent.
Shaffer, Lisa G; Agan, Noelle; Goldberg, James D; Ledbetter, David H; Longshore, John W; Cassidy, Suzanne B. American College of Medical Genetics Statement on Diagnostic Testing for Uniparental Disomy. Genetics in Medicine. 2001-05, 3 (3). ISSN 1098-3600. PMC 3111049 . PMID 11388763. doi:10.1097/00125817-200105000-00011.
Xin, Yalan; Fang, Hui; Yuan, Penghui; Jiang, Yushen. [Genetic analysis of an adult with mosaicism of uniparental disomy 11p]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 2019-12-10, 36 (12) [2024-01-16]. ISSN 1003-9406. PMID 31813152. doi:10.3760/cma.j.issn.1003-9406.2019.12.017. （原始内容存档于2024-01-16）.
Chantot-Bastaraud, Sandra; Stratmann, Svea; Brioude, Frédéric; Begemann, Matthias; Elbracht, Miriam; Graul-Neumann, Luitgard; Harbison, Madeleine; Netchine, Irène; Eggermann, Thomas. Formation of upd(7)mat by trisomic rescue: SNP array typing provides new insights in chromosomal nondisjunction. Molecular Cytogenetics. 2017-12, 10 (1) [2024-01-19]. ISSN 1755-8166. PMC 5526280 . PMID 28770003. doi:10.1186/s13039-017-0329-1. （原始内容存档于2023-02-25）（英语）.
Riveiro-Alvarez, R.; Valverde, D.; Lorda-Sanchez, I.; Trujillo-Tiebas, M. J.; Cantalapiedra, D.; Vallespin, E.; Aguirre-Lamban, J.; Ramos, C.; Ayuso, C. Partial paternal uniparental disomy (UPD) of chromosome 1 in a patient with Stargardt disease. Molecular Vision. 2007-01-26, 13 [2024-01-16]. ISSN 1090-0535. PMC 2553007 . PMID 17277736. （原始内容存档于2024-01-16）.
Shaffer, Lisa G; Agan, Noelle; Goldberg, James D; Ledbetter, David H; Longshore, John W; Cassidy, Suzanne B. American College of Medical Genetics Statement on Diagnostic Testing for Uniparental Disomy. Genetics in Medicine. 2001-05, 3 (3) [2024-01-17]. PMC 3111049 . PMID 11388763. doi:10.1097/00125817-200105000-00011. （原始内容存档于2023-11-18）（英语）.
Bis, Dana M.; Schüle, Rebecca; Reichbauer, Jennifer; Synofzik, Matthis; Rattay, Tim W.; Soehn, Anne; de Jonghe, Peter; Schöls, Ludger; Züchner, Stephan. Uniparental disomy determined by whole‐exome sequencing in a spectrum of rare motoneuron diseases and ataxias. Molecular Genetics & Genomic Medicine. 2017-05, 5 (3) [2024-01-28]. ISSN 2324-9269. PMC 5441426 . PMID 28546998. doi:10.1002/mgg3.285. （原始内容存档于2024-01-28）（英语）.
Yauy, Kevin; de Leeuw, Nicole; Yntema, Helger G.; Pfundt, Rolph; Gilissen, Christian. Accurate detection of clinically relevant uniparental disomy from exome sequencing data. Genetics in Medicine. 2020-04, 22 (4) [2024-01-28]. PMC 7118024 . PMID 31767986. doi:10.1038/s41436-019-0704-x. （原始内容存档于2024-04-12）（英语）.

pubmed.ncbi.nlm.nih.gov

Xin, Yalan; Fang, Hui; Yuan, Penghui; Jiang, Yushen. [Genetic analysis of an adult with mosaicism of uniparental disomy 11p]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 2019-12-10, 36 (12) [2024-01-16]. ISSN 1003-9406. PMID 31813152. doi:10.3760/cma.j.issn.1003-9406.2019.12.017. （原始内容存档于2024-01-16）.
Riveiro-Alvarez, R.; Valverde, D.; Lorda-Sanchez, I.; Trujillo-Tiebas, M. J.; Cantalapiedra, D.; Vallespin, E.; Aguirre-Lamban, J.; Ramos, C.; Ayuso, C. Partial paternal uniparental disomy (UPD) of chromosome 1 in a patient with Stargardt disease. Molecular Vision. 2007-01-26, 13 [2024-01-16]. ISSN 1090-0535. PMC 2553007 . PMID 17277736. （原始内容存档于2024-01-16）.

sciencedirect.com

Cook, Jackie. 7 - Genes in Families. Pyeritz, Reed E. (编). Emery and Rimoin's Principles and Practice of Medical Genetics and Genomics (Seventh Edition). Academic Press. 2019-01-01: 201–225 [2024-01-16]. ISBN 978-0-12-812537-3. doi:10.1016/b978-0-12-812537-3.00007-x. （原始内容存档于2022-04-03）.
Trent, Ronald J. 4 - COMPLEX GENETIC TRAITS. Trent, Ronald J (编). Molecular Medicine (Third Edition). Burlington: Academic Press. 2005-01-01: 77–118 [2024-01-16]. ISBN 978-0-12-699057-7. doi:10.1016/b978-012699057-7/50004-7. （原始内容存档于2022-04-03）.

sciengine.com

单亲二体及其在癌症中的作用研究进展. www.sciengine.com. [2024-01-16]. PMC 8800777 . PMID 31901032. doi:10.3785/j.issn.1008-9292.2019.10.15. （原始内容存档于2024-01-05）（中文）. Uniparental disomy (UPD) refers to a chromosome defect that an individual's homologous chromosome or segments are inherited from one parent.

web.archive.org

Benn, Peter. Uniparental disomy: Origin, frequency, and clinical significance. Prenatal Diagnosis. 2021-04, 41 (5) [2024-01-23]. ISSN 0197-3851. doi:10.1002/pd.5837. （原始内容存档于2024-01-08）（英语）.
单亲二体及其在癌症中的作用研究进展. www.sciengine.com. [2024-01-16]. PMC 8800777 . PMID 31901032. doi:10.3785/j.issn.1008-9292.2019.10.15. （原始内容存档于2024-01-05）（中文）. Uniparental disomy (UPD) refers to a chromosome defect that an individual's homologous chromosome or segments are inherited from one parent.
Engel, Eric. A new genetic concept: Uniparental disomy and its potential effect, isodisomy. American Journal of Medical Genetics. 1980-01, 6 (2) [2024-02-02]. ISSN 0148-7299. doi:10.1002/ajmg.1320060207. （原始内容存档于2024-02-02）（英语）.
崔婉婷赵彦艳. 染色体嵌合体及单亲二体的研究现状 Current research status on chromosomal mosaicism and uniparental disomy. 中华妇幼临床医学杂志(电子版). 2022 -04 -01 [2024-04-02]. doi:10.3877/cma.j.issn.1673-5250.2022.02.002. （原始内容存档于2024-04-03） –通过中华医学期刊全文数据库（中文）. 单亲二体(uniparental disomy，UPD)是指某一同源染色体均遗传自双亲之一请检查|date=中的日期值 (帮助)
Yamazawa, Kazuki; Ogata, Tsutomu; Ferguson‐Smith, Anne C. Uniparental disomy and human disease: An overview. American Journal of Medical Genetics Part C: Seminars in Medical Genetics. 2010-08-15, 154C (3) [2024-03-06]. ISSN 1552-4868. doi:10.1002/ajmg.c.30270. （原始内容存档于2024-04-30）（英语）.
Cook, Jackie. 7 - Genes in Families. Pyeritz, Reed E. (编). Emery and Rimoin's Principles and Practice of Medical Genetics and Genomics (Seventh Edition). Academic Press. 2019-01-01: 201–225 [2024-01-16]. ISBN 978-0-12-812537-3. doi:10.1016/b978-0-12-812537-3.00007-x. （原始内容存档于2022-04-03）.
Xin, Yalan; Fang, Hui; Yuan, Penghui; Jiang, Yushen. [Genetic analysis of an adult with mosaicism of uniparental disomy 11p]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 2019-12-10, 36 (12) [2024-01-16]. ISSN 1003-9406. PMID 31813152. doi:10.3760/cma.j.issn.1003-9406.2019.12.017. （原始内容存档于2024-01-16）.
Eggermann, Thomas; Soellner, Lukas; Buiting, Karin; Kotzot, Dieter. Mosaicism and uniparental disomy in prenatal diagnosis. Trends in Molecular Medicine. 2015-02, 21 (2) [2024-01-23]. ISSN 1471-4914. doi:10.1016/j.molmed.2014.11.010. （原始内容存档于2024-01-23）.
Wang, Y.; Li, Y.; Chen, Y.; Zhou, R.; Sang, Z.; Meng, L.; Tan, J.; Qiao, F.; Bao, Q.; Luo, D.; Peng, C. Systematic analysis of copy‐number variations associated with early pregnancy loss. Ultrasound in Obstetrics & Gynecology. 2020-01, 55 (1) [2024-02-02]. ISSN 0960-7692. doi:10.1002/uog.20412. （原始内容存档于2024-02-02）（英语）.
Trent, Ronald J. 4 - COMPLEX GENETIC TRAITS. Trent, Ronald J (编). Molecular Medicine (Third Edition). Burlington: Academic Press. 2005-01-01: 77–118 [2024-01-16]. ISBN 978-0-12-699057-7. doi:10.1016/b978-012699057-7/50004-7. （原始内容存档于2022-04-03）.
Chantot-Bastaraud, Sandra; Stratmann, Svea; Brioude, Frédéric; Begemann, Matthias; Elbracht, Miriam; Graul-Neumann, Luitgard; Harbison, Madeleine; Netchine, Irène; Eggermann, Thomas. Formation of upd(7)mat by trisomic rescue: SNP array typing provides new insights in chromosomal nondisjunction. Molecular Cytogenetics. 2017-12, 10 (1) [2024-01-19]. ISSN 1755-8166. PMC 5526280 . PMID 28770003. doi:10.1186/s13039-017-0329-1. （原始内容存档于2023-02-25）（英语）.
Riveiro-Alvarez, R.; Valverde, D.; Lorda-Sanchez, I.; Trujillo-Tiebas, M. J.; Cantalapiedra, D.; Vallespin, E.; Aguirre-Lamban, J.; Ramos, C.; Ayuso, C. Partial paternal uniparental disomy (UPD) of chromosome 1 in a patient with Stargardt disease. Molecular Vision. 2007-01-26, 13 [2024-01-16]. ISSN 1090-0535. PMC 2553007 . PMID 17277736. （原始内容存档于2024-01-16）.
Shaffer, Lisa G; Agan, Noelle; Goldberg, James D; Ledbetter, David H; Longshore, John W; Cassidy, Suzanne B. American College of Medical Genetics Statement on Diagnostic Testing for Uniparental Disomy. Genetics in Medicine. 2001-05, 3 (3) [2024-01-17]. PMC 3111049 . PMID 11388763. doi:10.1097/00125817-200105000-00011. （原始内容存档于2023-11-18）（英语）.
Bis, Dana M.; Schüle, Rebecca; Reichbauer, Jennifer; Synofzik, Matthis; Rattay, Tim W.; Soehn, Anne; de Jonghe, Peter; Schöls, Ludger; Züchner, Stephan. Uniparental disomy determined by whole‐exome sequencing in a spectrum of rare motoneuron diseases and ataxias. Molecular Genetics & Genomic Medicine. 2017-05, 5 (3) [2024-01-28]. ISSN 2324-9269. PMC 5441426 . PMID 28546998. doi:10.1002/mgg3.285. （原始内容存档于2024-01-28）（英语）.
Yauy, Kevin; de Leeuw, Nicole; Yntema, Helger G.; Pfundt, Rolph; Gilissen, Christian. Accurate detection of clinically relevant uniparental disomy from exome sequencing data. Genetics in Medicine. 2020-04, 22 (4) [2024-01-28]. PMC 7118024 . PMID 31767986. doi:10.1038/s41436-019-0704-x. （原始内容存档于2024-04-12）（英语）.

wiley.com

onlinelibrary.wiley.com

Engel, Eric. A new genetic concept: Uniparental disomy and its potential effect, isodisomy. American Journal of Medical Genetics. 1980-01, 6 (2) [2024-02-02]. ISSN 0148-7299. doi:10.1002/ajmg.1320060207. （原始内容存档于2024-02-02）（英语）.
Robinson, Wendy P. Mechanisms leading to uniparental disomy and their clinical consequences. BioEssays. 2000-04-24, 22 (5). doi:10.1002/(SICI)1521-1878(200005)22:5<452::AID-BIES7>3.0.CO;2-K （英语）. Uniparental disomy (UPD) refers to the situation in which both copies of a chromosome pair have originated from one parent.
Yamazawa, Kazuki; Ogata, Tsutomu; Ferguson‐Smith, Anne C. Uniparental disomy and human disease: An overview. American Journal of Medical Genetics Part C: Seminars in Medical Genetics. 2010-08-15, 154C (3) [2024-03-06]. ISSN 1552-4868. doi:10.1002/ajmg.c.30270. （原始内容存档于2024-04-30）（英语）.
Bis, Dana M.; Schüle, Rebecca; Reichbauer, Jennifer; Synofzik, Matthis; Rattay, Tim W.; Soehn, Anne; de Jonghe, Peter; Schöls, Ludger; Züchner, Stephan. Uniparental disomy determined by whole‐exome sequencing in a spectrum of rare motoneuron diseases and ataxias. Molecular Genetics & Genomic Medicine. 2017-05, 5 (3) [2024-01-28]. ISSN 2324-9269. PMC 5441426 . PMID 28546998. doi:10.1002/mgg3.285. （原始内容存档于2024-01-28）（英语）.

obgyn.onlinelibrary.wiley.com

Benn, Peter. Uniparental disomy: Origin, frequency, and clinical significance. Prenatal Diagnosis. 2021-04, 41 (5) [2024-01-23]. ISSN 0197-3851. doi:10.1002/pd.5837. （原始内容存档于2024-01-08）（英语）.
Wang, Y.; Li, Y.; Chen, Y.; Zhou, R.; Sang, Z.; Meng, L.; Tan, J.; Qiao, F.; Bao, Q.; Luo, D.; Peng, C. Systematic analysis of copy‐number variations associated with early pregnancy loss. Ultrasound in Obstetrics & Gynecology. 2020-01, 55 (1) [2024-02-02]. ISSN 0960-7692. doi:10.1002/uog.20412. （原始内容存档于2024-02-02）（英语）.

worldcat.org

Benn, Peter. Uniparental disomy: Origin, frequency, and clinical significance. Prenatal Diagnosis. 2021-04, 41 (5) [2024-01-23]. ISSN 0197-3851. doi:10.1002/pd.5837. （原始内容存档于2024-01-08）（英语）.
Shaffer, Lisa G; Agan, Noelle; Goldberg, James D; Ledbetter, David H; Longshore, John W; Cassidy, Suzanne B. American College of Medical Genetics Statement on Diagnostic Testing for Uniparental Disomy. Genetics in Medicine. 2001-05, 3 (3). ISSN 1098-3600. PMC 3111049 . PMID 11388763. doi:10.1097/00125817-200105000-00011.
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崔婉婷赵彦艳. 染色体嵌合体及单亲二体的研究现状 Current research status on chromosomal mosaicism and uniparental disomy. 中华妇幼临床医学杂志(电子版). 2022 -04 -01 [2024-04-02]. doi:10.3877/cma.j.issn.1673-5250.2022.02.002. （原始内容存档于2024-04-03） –通过中华医学期刊全文数据库（中文）. 单亲二体(uniparental disomy，UPD)是指某一同源染色体均遗传自双亲之一请检查|date=中的日期值 (帮助)