221 related articles for article (PubMed ID: 31807870)
1. Multiple methods used for type detection of uniparental disomy in paternity testing.
Su H; Sun T; Chen M; Liu J; Wang X; Chen Y; Ren W; Zhang G; Yan J; Yun K
Int J Legal Med; 2020 May; 134(3):885-893. PubMed ID: 31807870
[TBL] [Abstract][Full Text] [Related]
2. Effect of uniparental disomy in parentage testing.
Ma D; Lin Y; Zhang R; Wang S; Hu W; Ye M; Gao H; Wang L; Song Y; Guo H
Leg Med (Tokyo); 2024 Mar; 67():102381. PubMed ID: 38154315
[TBL] [Abstract][Full Text] [Related]
3. [Influence of uniparental disomy on the conclusion of paternity testing].
Kang B; Wu D; Wang X; Wang H; He M; Liao S
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Sep; 36(9):938-942. PubMed ID: 31515795
[TBL] [Abstract][Full Text] [Related]
4. Non-pathological complete paternal uniparental isodisomy of chromosome 2 revealed in a maternity testing case.
Chen M; Jiang J; Li C; Ren H; Chen W; Liu Z; Cheng F; Zhao J; Chen T; Chen C; Yan J
Int J Legal Med; 2019 Jul; 133(4):993-997. PubMed ID: 29802460
[TBL] [Abstract][Full Text] [Related]
5. Complete Paternal Uniparental Disomy of Chromosome 2 in an Asian Female Identified by Short Tandem Repeats and Whole Genome Sequencing.
Zhang X; Ding Z; He R; Qi J; Zhang Z; Cui B
Cytogenet Genome Res; 2019; 157(4):197-202. PubMed ID: 30991391
[TBL] [Abstract][Full Text] [Related]
6. Maternal uniparental disomy of chromosome 21 as a cause of pseudo-exclusion from paternity.
Semikhodskii A; Makarova T; Sutyagina D
Mol Genet Genomics; 2023 Nov; 298(6):1389-1394. PubMed ID: 37656271
[TBL] [Abstract][Full Text] [Related]
7. Confirmation of Paternity despite Three Genetic Incompatibilities at Chromosome 2.
Doniec A; Łuczak W; Wróbel M; Januła M; Ossowski A; Grzmil P; Kupiec T
Genes (Basel); 2021 Jan; 12(1):. PubMed ID: 33406744
[TBL] [Abstract][Full Text] [Related]
8. SNP chromosome microarray genotyping for detection of uniparental disomy in the clinical diagnostic laboratory.
Ngo C; Baluyot M; Bennetts B; Carmichael J; Clark A; Darmanian A; Gayagay T; Jones L; Nash B; Clark M; Jose N; Robinson S; St Heaps L; Wright D
Pathology; 2023 Oct; 55(6):818-826. PubMed ID: 37414616
[TBL] [Abstract][Full Text] [Related]
9. Case reports on uniparental disomy of chromosomes 6 and 3 in paternity testing.
Ren H; Liu Z; Chen C; Shi Y; Zhang J; Chen Y; Jia L; Liu Y; Yan J
Forensic Sci Res; 2024 Jun; 9(2):owae027. PubMed ID: 38774862
[TBL] [Abstract][Full Text] [Related]
10. Global analysis of uniparental disomy using high density genotyping arrays.
Bruce S; Leinonen R; Lindgren CM; Kivinen K; Dahlman-Wright K; Lipsanen-Nyman M; Hannula-Jouppi K; Kere J
J Med Genet; 2005 Nov; 42(11):847-51. PubMed ID: 15879501
[TBL] [Abstract][Full Text] [Related]
11. UPD detection using homozygosity profiling with a SNP genotyping microarray.
Papenhausen P; Schwartz S; Risheg H; Keitges E; Gadi I; Burnside RD; Jaswaney V; Pappas J; Pasion R; Friedman K; Tepperberg J
Am J Med Genet A; 2011 Apr; 155A(4):757-68. PubMed ID: 21594998
[TBL] [Abstract][Full Text] [Related]
12. Complete paternal uniparental isodisomy for Chromosome 2 revealed in a parentage testing case.
Ou X; Liu C; Chen S; Yu J; Zhang Y; Liu S; Sun H
Transfusion; 2013 Jun; 53(6):1266-9. PubMed ID: 22924962
[TBL] [Abstract][Full Text] [Related]
13. Uniparental disomy of chromosome 21: A statistical approach and application in paternity tests.
Cavalheiro CP; Avila E; Gastaldo AZ; Graebin P; Motta CHA; Rodenbusch R; Alho CS
Forensic Sci Int Genet; 2020 Nov; 49():102368. PubMed ID: 32911454
[TBL] [Abstract][Full Text] [Related]
14. Inference of maternal uniparental disomy of the entire chromosome 2 from a paternity test.
Guzmán-Alberto JC; Martínez-Cortes G; Rangel-Villalobos H
Int J Legal Med; 2019 Jan; 133(1):71-75. PubMed ID: 29511852
[TBL] [Abstract][Full Text] [Related]
15. Loss of heterozygosity detected at three short tandem repeat locus commonly used for human DNA identification in a case of paternity testing.
Zhou S; Wang H; Wang QK; Wang P; Wang F; Xu C
Leg Med (Tokyo); 2017 Jan; 24():7-11. PubMed ID: 28081793
[TBL] [Abstract][Full Text] [Related]
16. Detection of Hereditary 1,25-Hydroxyvitamin D-Resistant Rickets Caused by Uniparental Disomy of Chromosome 12 Using Genome-Wide Single Nucleotide Polymorphism Array.
Tamura M; Isojima T; Kawashima M; Yoshida H; Yamamoto K; Kitaoka T; Namba N; Oka A; Ozono K; Tokunaga K; Kitanaka S
PLoS One; 2015; 10(7):e0131157. PubMed ID: 26153892
[TBL] [Abstract][Full Text] [Related]
17. Rapid Diagnosis of Imprinting Disorders Involving Copy Number Variation and Uniparental Disomy Using Genome-Wide SNP Microarrays.
Liu W; Zhang R; Wei J; Zhang H; Yu G; Li Z; Chen M; Sun X
Cytogenet Genome Res; 2015; 146(1):9-18. PubMed ID: 26184742
[TBL] [Abstract][Full Text] [Related]
18. Uniparental disomy in the human blastocyst is exceedingly rare.
Gueye NA; Devkota B; Taylor D; Pfundt R; Scott RT; Treff NR
Fertil Steril; 2014 Jan; 101(1):232-6. PubMed ID: 24083874
[TBL] [Abstract][Full Text] [Related]
19. Contribution of uniparental disomy in a clinical trio exome cohort of 2675 patients.
Wang L; Liu P; Bi W; Sim T; Wang X; Walkiewicz M; Leduc MS; Meng L; Xia F; Eng CM; Yang Y; Yuan B; Dai H
Mol Genet Genomic Med; 2021 Nov; 9(11):e1792. PubMed ID: 34587367
[TBL] [Abstract][Full Text] [Related]
20. Uniparental disomy analysis in trios using genome-wide SNP array and whole-genome sequencing data imply segmental uniparental isodisomy in general populations.
Sasaki K; Mishima H; Miura K; Yoshiura K
Gene; 2013 Jan; 512(2):267-74. PubMed ID: 23111162
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
