PubMed for id: 272854

Year	Number of Results
1980	1
1984	2
1986	1
1991	2
1992	5
1993	6
1994	4
1995	2
1996	7
1997	5
1998	5
1999	2
2000	10
2001	1
2002	3
2003	6
2004	9
2005	4
2006	5
2007	5
2008	2
2009	1
2010	3
2012	2
2013	1
2014	3
2015	2
2016	3
2017	4
2018	1
2020	1
2021	2
2022	3
2023	0

1

Germline CHEK2 and ATM Variants in Myeloid and Other Hematopoietic Malignancies.

Stubbins RJ, Korotev S, Godley LA. Stubbins RJ, et al. Curr Hematol Malig Rep. 2022 Aug;17(4):94-104. doi: 10.1007/s11899-022-00663-7. Epub 2022 Jun 8. Curr Hematol Malig Rep. 2022. PMID: 35674998 Review.

2

Typical, atypical and cryptic t(15;17)(q24;q21) (PML::RARA) observed in acute promyelocytic leukemia: A retrospective review of 831 patients with concurrent chromosome and PML::RARA dual-color dual-fusion FISH studies.

Gagnon MF, Berg HE, Meyer RG, Sukov WR, Van Dyke DL, Jenkins RB, Greipp PT, Thorland EC, Hoppman NL, Xu X, Baughn LB, Reichard KK, Ketterling RP, Peterson JF. Gagnon MF, et al. Genes Chromosomes Cancer. 2022 Oct;61(10):629-634. doi: 10.1002/gcc.23070. Epub 2022 Jun 10. Genes Chromosomes Cancer. 2022. PMID: 35639830

3

A novel coexistence of tetrasomy 8 and FLT3-ITD along with variant 3 way translocation t(4;17;15) in acute promyelocytic leukemia: Case study and literature review.

Pais A, Fernandes C, Dalvi R, Bafna V, Pawar R, Chavan D, Ahmad F. Pais A, et al. Cancer Genet. 2022 Apr;262-263:111-117. doi: 10.1016/j.cancergen.2022.02.004. Epub 2022 Feb 16. Cancer Genet. 2022. PMID: 35219054 Review.

4

Drug resistance in diploid yeast is acquired through dominant alleles, haploinsufficiency, gene duplication and aneuploidy.

Barney JB, Chandrashekarappa DG, Soncini SR, Schmidt MC. Barney JB, et al. PLoS Genet. 2021 Sep 23;17(9):e1009800. doi: 10.1371/journal.pgen.1009800. eCollection 2021 Sep. PLoS Genet. 2021. PMID: 34555030 Free PMC article.

5

Tetrasomy of 11q13.4-q14.3 due to an intrachromosomal triplication associated with paternal uniparental isodisomy for 11q14.3-qter, intrauterine growth restriction, developmental delay, corpus callosum dysgenesis, microcephaly, congenital heart defects and facial dysmorphism.

Chen CP, Lin SP, Chern SR, Wu PS, Chen SW, Wu FT, Town DD, Wang W. Chen CP, et al. Taiwan J Obstet Gynecol. 2021 Jan;60(1):169-172. doi: 10.1016/j.tjog.2020.11.027. Taiwan J Obstet Gynecol. 2021. PMID: 33494996 Free article.

6

Cytogenetic Investigation in 136 Consecutive Stillbirths: Does the Tissue Type Affect the Success Rate of Chromosomal Microarray Analysis and Karyotype?

Marquès B, Benitez L, Peguero A, Madrigal I, Gómez O, Figueras F, Borrell A. Marquès B, et al. Fetal Diagn Ther. 2020;47(4):315-320. doi: 10.1159/000505399. Epub 2020 Jan 17. Fetal Diagn Ther. 2020. PMID: 31955157

7

Fetoplacental cytogenetic discrepancy in a pregnancy with fetal mosaic tetrasomy 12p and Pallister-Killian syndrome detected by amniocentesis.

Chen CP, Wang LK, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Chen LF, Wang W. Chen CP, et al. Taiwan J Obstet Gynecol. 2017 Dec;56(6):852-856. doi: 10.1016/j.tjog.2017.10.034. Taiwan J Obstet Gynecol. 2017. PMID: 29241934 Free article.

8

Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaicism for tetrasomy 18p at amniocentesis in a pregnancy with a favorable outcome.

Chen CP, Ko TM, Chen YY, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Yang CW, Pan CW, Wang W. Chen CP, et al. Taiwan J Obstet Gynecol. 2017 Dec;56(6):836-839. doi: 10.1016/j.tjog.2017.10.024. Taiwan J Obstet Gynecol. 2017. PMID: 29241930 Free article.

9

A review of structural brain abnormalities in Pallister-Killian syndrome.

Poulton C, Baynam G, Yates C, Alinejad-Rokny H, Williams S, Wright H, Woodward KJ, Sivamoorthy S, Peverall J, Shipman P, Ravine D, Beilby J, Heng JI. Poulton C, et al. Mol Genet Genomic Med. 2018 Jan;6(1):92-98. doi: 10.1002/mgg3.351. Epub 2017 Dec 9. Mol Genet Genomic Med. 2018. PMID: 29222831 Free PMC article. Review.

10

Pallister-Killian syndrome: Cytogenetics and molecular investigations of mosaic tetrasomy 12p in prenatal chorionic villus and in amniocytes. Strategy of prenatal diagnosis.

Libotte F, Bizzoco D, Gabrielli I, Mesoraca A, Cignini P, Vitale SG, Marilli I, Gulino FA, Rapisarda AM, Giorlandino C. Libotte F, et al. Taiwan J Obstet Gynecol. 2016 Dec;55(6):863-866. doi: 10.1016/j.tjog.2016.07.010. Taiwan J Obstet Gynecol. 2016. PMID: 28040135 Free article.

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