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Select item 82466601.

Single-cell chromatin accessibility landscape of human umbilical cord blood in trisomy 18 syndrome

Xiaofen Qiu, Haiyan Yu, Hongwei Wu, Zhiyang Hu, Jun Zhou, Hua Lin, Wen Xue, Wanxia Cai, Jiejing Chen, Qiang Yan, Weier Dai, Ming Yang, Donge Tang, Yong Dai

Hum Genomics. 2021; 15: 40. Published online 2021 Jun 30. doi: 10.1186/s40246-021-00338-z

PMCID:: PMC8246660

Abstract Article PDF–2.8M

Select item 56809282.

The spontaneous differentiation and chromosome loss in iPSCs of human trisomy 18 syndrome

Ting Li, Hanzhi Zhao, Xu Han, Jiaying Yao, Lingling Zhang, Ying Guo, Zhen Shao, Ying Jin, Dongmei Lai

Cell Death Dis. 2017 Oct; 8(10): e3149. Published online 2017 Oct 26. doi: 10.1038/cddis.2017.565

PMCID:: PMC5680928

Abstract Article PDF–4.3M

Select item 49498023.

Trisomy 18 syndrome: Towards a balanced approach

Hassan Batees, Khalid A Altirkawi

Sudan J Paediatr. 2014; 14(2): 76–84.

PMCID:: PMC4949802

Abstract Article PDF–2.5M

Select item 35208244.

The trisomy 18 syndrome

Anna Cereda, John C Carey

Orphanet J Rare Dis. 2012; 7: 81. Published online 2012 Oct 23. doi: 10.1186/1750-1172-7-81

PMCID:: PMC3520824

Abstract Article PDF–1.3M

Select item 14985235.

Decrease in gamma-glutamyl transpeptidase activity in early amniotic fluid in fetal trisomy 18 syndrome.

H Janlanko, P Aula

Br Med J (Clin Res Ed) 1982 May 29; 284(6329): 1593–1594. doi: 10.1136/bmj.284.6329.1593

PMCID:: PMC1498523

Summary Page Browse PDF–354K

Select item 10800376.

Trisomy 18 syndrome with cleft foot.

D Castle, R Bernstein

J Med Genet. 1988 Aug; 25(8): 568–570. doi: 10.1136/jmg.25.8.568

PMCID:: PMC1080037

Summary Page Browse PDF–633K

Select item 10493017.

Four cases of trisomy 18 syndrome with limb reduction malformations.

A L Christianson, M M Nelson

J Med Genet. 1984 Aug; 21(4): 293–297. doi: 10.1136/jmg.21.4.293

PMCID:: PMC1049301

Summary Page Browse PDF–907K

Select item 10128288.

Trisomy 18 syndrome with an unusual karyotype: possible double isochromosome.

L M Larson, W A Wasdahl, J H Saumur, M L Coleman, S M Jalal

J Med Genet. 1978 Feb; 15(1): 73–76. doi: 10.1136/jmg.15.1.73

PMCID:: PMC1012828

Summary Page Browse PDF–1.0M

Select item 110817949.

Cardiac care in trisomy 18: A path to improved outcomes (case report)

Abdullghany Dowaikh, Atif Alsahari, Saad Khoshhal, Tarek Momenah

J Taibah Univ Med Sci. 2024 Jun; 19(3): 545–548. Published online 2024 Apr 25. doi: 10.1016/j.jtumed.2024.04.003

PMCID:: PMC11081794

Abstract Article PDF–1.9M

Select item 1107346310.

Anesthetic Management of a Patient With Trisomy 18 Undergoing a Multilevel Spinal Fusion

Davis Frease, David Rico Mora

J Med Cases. 2024 May; 15(4-5): 78–81. Published online 2024 May 2. doi: 10.14740/jmc4202

PMCID:: PMC11073463

Abstract Article PDF–237K

Select item 1104981511.

Therapeutic Management and Outcomes of Hepatoblastoma in a Pediatric Patient with Mosaic Edwards Syndrome

Patrycja Sosnowska-Sienkiewicz, Alicja Kamińska, Iwona Anderko, Gabriela Telman-Kołodziejczyk, Przemysław Mańkowski, Danuta Januszkiewicz-Lewandowska

Genes (Basel) 2024 Apr; 15(4): 463. Published online 2024 Apr 7. doi: 10.3390/genes15040463

PMCID:: PMC11049815

Abstract Article PDF–752K

Select item 1089861212.

A Rare Presentation of Edwards Syndrome in a Three-Month-Old Infant: A Case Report

Anirudh Kommareddy, Jayant D Vagha, Keta Vagha, Amar Taksande, Chaitanya Kumar Javvaji

Cureus. 2024 Jan; 16(1): e53105. Published online 2024 Jan 28. doi: 10.7759/cureus.53105

PMCID:: PMC10898612

Abstract Article PDF–1.1M

Select item 1087916513.

Cases of trisomy 21 and trisomy 18 among historic and prehistoric individuals discovered from ancient DNA

Adam Benjamin Rohrlach, Maïté Rivollat, Patxuka de-Miguel-Ibáñez, Ulla Moilanen, Anne-Mari Liira, João C. Teixeira, Xavier Roca-Rada, Javier Armendáriz-Martija, Kamen Boyadzhiev, Yavor Boyadzhiev, Bastien Llamas, Anthi Tiliakou, Angela Mötsch, Jonathan Tuke, Eleni-Anna Prevedorou, Naya Polychronakou-Sgouritsa, Jane Buikstra, Päivi Onkamo, Philipp W. Stockhammer, Henrike O. Heyne, Johannes R. Lemke, Roberto Risch, Stephan Schiffels, Johannes Krause, Wolfgang Haak, Kay Prüfer

Nat Commun. 2024; 15: 1294. Published online 2024 Feb 20. doi: 10.1038/s41467-024-45438-1

PMCID:: PMC10879165

Abstract Article PDF–1000K

Select item 1087636214.

Coorte retrospectiva de trissomia do cromossomo 18 (síndrome de Edwards) no sul do Brasil: Retrospective cohort of trisomy 18 (Edwards syndrome) in southern Brazil

Daniela Denardin, Fabíola Elizabete Savaris, André Campos da Cunha, Rosilene da Silveira Betat, Jorge Alberto Bianchi Telles, Luciano Vieira Targa, Aline Weiss, Paulo Ricardo Gazzola Zen, Rafael Fabiano Machado Rosa

Sao Paulo Med J. 2015; 133(4): 320–325. Published online 2014 Nov 7. doi: 10.1590/1516-3180.2013.79900715