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Items: 1 to 20 of 36

1.
Genome-wide interaction analysis of folate for colorectal cancer risk
Emmanouil Bouras, Andre E. Kim, Yi Lin, John Morrison, Mengmeng Du, Demetrius Albanes, Elizabeth L. Barry, James W. Baurley, Sonja I. Berndt, Stephanie A. Bien, Timothy D. Bishop, Hermann Brenner, Arif Budiarto, Andrea Burnett-Hartman, Peter T. Campbell, Robert Carreras-Torres, Graham Casey, Tjeng Wawan Cenggoro, Andrew T. Chan, Jenny Chang-Claude, David V. Conti, Michelle Cotterchio, Matthew Devall, Virginia Diez-Obrero, Niki Dimou, David A. Drew, Jane C. Figueiredo, Graham G. Giles, Stephen B. Gruber, Marc J. Gunter, Tabitha A. Harrison, Akihisa Hidaka, Michael Hoffmeister, Jeroen R. Huyghe, Amit D. Joshi, Eric S. Kawaguchi, Temitope O. Keku, Anshul Kundaje, Loic Le Marchand, Juan Pablo Lewinger, Li Li, Brigid M. Lynch, Bharuno Mahesworo, Satu Männistö, Victor Moreno, Neil Murphy, Polly A. Newcomb, Mireia Obón-Santacana, Jennifer Ose, Julie R. Palmer, Nikos Papadimitriou, Bens Pardamean, Andrew J. Pellatt, Anita R. Peoples, Elizabeth A. Platz, John D. Potter, Lihong Qi, Conghui Qu, Gad Rennert, Edward Ruiz-Narvaez, Lori C. Sakoda, Stephanie L. Schmit, Anna Shcherbina, Mariana C. Stern, Yu-Ru Su, Catherine M. Tangen, Duncan C. Thomas, Yu Tian, Caroline Y. Um, Franzel JB. van Duijnhoven, Bethany Van Guelpen, Kala Visvanathan, Jun Wang, Emily White, Alicja Wolk, Michael O. Woods, Cornelia M. Ulrich, Li Hsu, W James Gauderman, Ulrike Peters, Konstantinos K. Tsilidis
Am J Clin Nutr. 2023 Nov; 118(5): 881–891. Published online 2023 Aug 26. doi: 10.1016/j.ajcnut.2023.08.010
PMCID:
PMC10636229
AbstractArticlePDF–1.3M
2.
3q26.2/MECOM Rearrangements by Pericentric Inv(3): Diagnostic Challenges and Clinicopathologic Features
Zhenya Tang, Wei Wang, Su Yang, Hanadi El Achi, Hong Fang, Karen Amelia Nahmod, Gokce A. Toruner, Jie Xu, Beenu Thakral, Edward Ayoub, Ghayas C. Issa, C. Cameron Yin, M. James You, Roberto N. Miranda, Joseph D. Khoury, L. Jeffrey Medeiros, Guilin Tang
Cancers (Basel) 2023 Jan; 15(2): 458. Published online 2023 Jan 11. doi: 10.3390/cancers15020458
PMCID:
PMC9856433
AbstractArticlePDF–1.6M
3.
Partial Trisomy 13q/Monosomy 3p Resulting from a Paternal Reciprocal 3p;13q Translocation in a Boy with Facial Dysmorphism and Hypertrophic Cardiomyopathy
Monica Martin-de Saro, Zyndia Compean, Karina Aguilar, Luz María González-Huerta, Lautaro Plaza-Benhumea, Olga Messina-Baas, Sergio Alberto Cuevas-Covarrubiass
Mol Syndromol. 2021 Aug; 12(5): 305–311. Published online 2021 Jul 20. doi: 10.1159/000516058
PMCID:
PMC8436647
AbstractArticlePDF–396K
4.
Case Report: A Case Report and Literature Review of 3p Deletion Syndrome
Junxian Fu, Ting Wang, Zhuo Fu, Tianxia Li, Xiaomeng Zhang, Jingjing Zhao, Guanglu Yang
Front Pediatr. 2021; 9: 618059. Published online 2021 Feb 10. doi: 10.3389/fped.2021.618059
PMCID:
PMC7902511
AbstractArticlePDF–398K
5.
Application of array comparative genomic hybridization in Korean children under 6 years old with global developmental delay
Kyung Yeon Lee, Eunsim Shin
Korean J Pediatr. 2017 Sep; 60(9): 282–289. Published online 2017 Sep 21. doi: 10.3345/kjp.2017.60.9.282
PMCID:
PMC5638834
AbstractArticlePDF–645K
6.
Chromosome Rearrangements in Cornelia de Lange Syndrome (CdLS): Report of a der(3)t(3;12)(p25.3;p13.3) in Two Half Sibs With Features of CdLS and Review of Reported CdLS Cases With Chromosome Rearrangements
Cheryl DeScipio, Maninder Kaur, Dinah Yaeger, Jeffrey W. Innis, Nancy B. Spinner, Laird G. Jackson, Ian D. Krantz
Am J Med Genet A. Author manuscript; available in PMC 2016 Jun 7.
Published in final edited form as: Am J Med Genet A. 2005 Sep 1; 137A(3): 276–282. doi: 10.1002/ajmg.a.30857
PMCID:
PMC4896149
AbstractArticlePDF–364K
7.
Trisomy 1q41-qter and monosomy 3p26.3-pter in a family with a translocation (1;3): further delineation of the syndromes
Alicia Cervantes, Constanza García-Delgado, Fernando Fernández-Ramírez, Carolina Galaz-Montoya, Ariadna Berenice Morales-Jiménez, Karem Nieto-Martínez, Laura Gómez-Laguna, Judith Villa-Morales, Mónica Quintana-Palma, Jaime Berúmen, Susana Kofman, Verónica F Morán-Barroso
BMC Med Genomics. 2014; 7: 55. Published online 2014 Sep 15. doi: 10.1186/1755-8794-7-55
PMCID:
PMC4170088
AbstractArticlePDF–2.2M
8.
A familial inverted duplication/deletion of 2p25.1–25.3 provides new clues on the genesis of inverted duplications
Maria Clara Bonaglia, Roberto Giorda, Angelo Massagli, Rita Galluzzi, Roberto Ciccone, Orsetta Zuffardi
Eur J Hum Genet. 2009 Feb; 17(2): 179–186. Published online 2008 Sep 24. doi: 10.1038/ejhg.2008.160
PMCID:
PMC2986066
AbstractArticlePDF–312K
9.
3p-Syndrome Defines a Hearing Loss Locus in 3p25.3
Brendan J. McCullough, Joe C. Adams, Dustin J. Shilling, M. Patrick Feeney, Kathleen C. Y. Sie, Bruce L Tempel
Hear Res. Author manuscript; available in PMC 2007 Sep 30.
Published in final edited form as: Hear Res. 2007 Feb; 224(1-2): 51–60. Published online 2007 Jan 8. doi: 10.1016/j.heares.2006.11.006
PMCID:
PMC1995240
AbstractArticlePDF–350K
10.
Congenital variant Rett syndrome in a girl with terminal deletion of chromosome 3p
J. Wahlstrom, A. Uller, T. Johannesson, D. Holmqvist, C. Darnfors, M. Vujic, B. Tonnby, B. Hagberg, T. Martinsson
J Med Genet. 1999 Apr; 36(4): 343–345.
PMCID:
PMC1734344
SummaryPDF–120K
11.
Disruption of Contactin 4 (CNTN4) Results in Developmental Delay and Other Features of 3p Deletion Syndrome
Thomas Fernandez, Thomas Morgan, Nicole Davis, Ami Klin, Ashley Morris, Anita Farhi, Richard P. Lifton, Matthew W. State
Am J Hum Genet. 2004 Jun; 74(6): 1286–1293. Published online 2004 Apr 21. doi: 10.1086/421474
PMCID:
PMC1182094
AbstractArticlePDF–402K
12.
Precise localisation of 3p25 breakpoints in four patients with the 3p-syndrome.
T Drumheller, B C McGillivray, D Behrner, P MacLeod, D E McFadden, J Roberson, C Venditti, K Chorney, M Chorney, D I Smith
J Med Genet. 1996 Oct; 33(10): 842–847. doi: 10.1136/jmg.33.10.842
PMCID:
PMC1050764
SummaryPage BrowsePDF–1.2M
13.
Three children with partial trisomy 1q and partial monosomy 3p.
G T McCarthy, C N Fear, A C Berry
J Med Genet. 1986 Oct; 23(5): 466–467. doi: 10.1136/jmg.23.5.466
PMCID:
PMC1049787
SummaryPage BrowsePDF–390K
14.
Duplication-deletion with partial trisomy lq and partial monosomy 3p resulting from a maternal reciprocal translocation rcp (1;3) (q32;p25).
A Schinzel
J Med Genet. 1981 Feb; 18(1): 64–68. doi: 10.1136/jmg.18.1.64
PMCID:
PMC1048662
SummaryPage BrowsePDF–1.0M
15.
Detailed mapping of a congenital heart disease gene in chromosome 3p25
E. Green, M. Priestley, J. Waters, C. Maliszewska, F. Latif, E. Maher
J Med Genet. 2000 Aug; 37(8): 581–587. doi: 10.1136/jmg.37.8.581
PMCID:
PMC1734659
SummaryPDF–205K
16.
Segregation of a t(3;20) translocation through three generations resulting in unbalanced karyotypes in six persons.
K B Nielsen, N Tommerup, B Jespersen, P Nygaard, L Kleif
J Med Genet. 1986 Oct; 23(5): 446–451. doi: 10.1136/jmg.23.5.446
PMCID:
PMC1049782
SummaryPage BrowsePDF–885K
17.
The phenotype of ring chromosome 3.
G N Wilson, J Pooley, J Parker
J Med Genet. 1982 Dec; 19(6): 471–473. doi: 10.1136/jmg.19.6.471
PMCID:
PMC1048968
SummaryPage BrowsePDF–557K
18.
The novel Rho-GTPase activating gene MEGAP/ srGAP3 has a putative role in severe mental retardation
Volker Endris, Birgit Wogatzky, Uwe Leimer, Dusan Bartsch, Malgorzata Zatyka, Farida Latif, Eamonn R. Maher, Gholamali Tariverdian, Stefan Kirsch, Dieter Karch, Gudrun A. Rappold
Proc Natl Acad Sci U S A. 2002 Sep 3; 99(18): 11754–11759. Published online 2002 Aug 23. doi: 10.1073/pnas.162241099
PMCID:
PMC129341
AbstractArticlePDF–326K
19.
Fetal Cystic Hygroma Associated with Terminal 2p25.1 Duplication and Terminal 3p25.3 Deletion: Cytogenetic, Fluorescent in Situ Hybridization and Microarray Familial Characterization of Two Different Chromosomal Structural Rearrangements
Associate Professor F Stipoljev, M Barbalic, M Logara, A Vicic, M Vulic, S Zekic Tomas, R Gjergja Juraski
Balkan J Med Genet. 2020 Nov; 23(2): 79–86. Published online 2021 Mar 23. doi: 10.2478/bjmg-2020-0023
PMCID:
PMC8009571
AbstractArticlePDF–1020K
20.
Monosomy 3 Influences Epithelial-Mesenchymal Transition Gene Expression in Uveal Melanoma Patients; Consequences for Liquid Biopsy
Andrea Soltysova, Tatiana Sedlackova, Dana Dvorska, Karin Jasek, Pooneh Chokhachi Baradaran, Viera Horvathova Kajabova, Lucia Demkova, Verona Buocikova, Terezia Kurucova, Darina Lyskova, Alena Furdova, Gabriel Minarik, Pavel Babal, Zuzana Dankova, Bozena Smolkova
Int J Mol Sci. 2020 Dec; 21(24): 9651. Published online 2020 Dec 17. doi: 10.3390/ijms21249651
PMCID:
PMC7767066
AbstractArticlePDF–11M

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