BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

263 related articles for article (PubMed ID: 19215885)

  • 1. A paternity case with three genetic incompatibilities between father and child due to maternal uniparental disomy 21 and a mutation at the Y chromosome.
    Mansuet-Lupo A; Henke J; Henke L; Blank C; Ernsting A; Kozlowski P; Rouger P; Van Huffel V
    Forensic Sci Int Genet; 2009 Mar; 3(2):141-3. PubMed ID: 19215885
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Paternal uniparental isodisomy of the entire chromosome 3 revealed in a person with no apparent phenotypic disorders.
    Xiao P; Liu P; Weber JL; Papasian CJ; Recker RR; Deng HW
    Hum Mutat; 2006 Feb; 27(2):133-7. PubMed ID: 16429396
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Maternal uniparental disomy (UPD) for chromosome 2 discovered by exclusion of paternity.
    Heide E; Heide KG; Rodewald A
    Am J Med Genet; 2000 Jun; 92(4):260-3. PubMed ID: 10842292
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Pseudo-exclusion from paternity due to maternal uniparental disomy 16.
    Bein G; Driller B; Schürmann M; Schneider PM; Kirchner H
    Int J Legal Med; 1998; 111(6):328-30. PubMed ID: 9826094
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Kinship determination using DNA markers].
    Jorquera G H; Acuña P M; Cifuentes L L
    Rev Med Chil; 2008 Feb; 136(2):193-200. PubMed ID: 18483673
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Prader-Willi syndrome due to uniparental disomy in a patient with a balanced chromosomal translocation.
    Calounova G; Novotna D; Simandlova M; Havlovicova M; Zumrová A; Kocarek E; Sedlacek Z
    Neuro Endocrinol Lett; 2006 Oct; 27(5):579-85. PubMed ID: 17159828
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Two fathers for the same child: a deficient paternity case of false inclusion with autosomic STRs.
    González-Andrade F; Sánchez D; Penacino G; Martínez Jarreta B
    Forensic Sci Int Genet; 2009 Mar; 3(2):138-40. PubMed ID: 19215884
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mutation in the STR locus D21S1 1 of father causing allele mismatch in the child.
    Thangaraj K; Reddy AG; Singh L
    J Forensic Sci; 2004 Jan; 49(1):99-103. PubMed ID: 14979352
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Exclusion of uniparental inheritance of chromosome 15 in a fetus with a familial dicentric (Y;15) translocation.
    White LM; Treat K; Leff A; Styers D; Mitchell M; Knoll JH
    Prenat Diagn; 1998 Feb; 18(2):111-6. PubMed ID: 9516010
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A case of segmental paternal isodisomy of chromosome 14.
    Coveler KJ; Yang SP; Sutton R; Milstein JM; Wu YQ; Bois KD; Beischel LS; Johnson JP; Shaffer LG
    Hum Genet; 2002 Mar; 110(3):251-6. PubMed ID: 11935337
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Uniparental disomy of chromosome 2 resulting in lethal trifunctional protein deficiency due to homozygous alpha-subunit mutations.
    Spiekerkoetter U; Eeds A; Yue Z; Haines J; Strauss AW; Summar M
    Hum Mutat; 2002 Dec; 20(6):447-51. PubMed ID: 12442268
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [An unusual case of investigation into the child's disputable descent complicated by manifestation of a rare genomic mutation (disomy)].
    Ivanov PL; Bin'ko IA; Orekhov VA
    Sud Med Ekspert; 2010; 53(1):38-43. PubMed ID: 20394199
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Paternal isodisomy for chromosome 2 as the cause of Crigler-Najjar type I syndrome.
    Petit FM; Gajdos V; Parisot F; Capel L; Aboura A; Lachaux A; Tachdjian G; Poüs C; Labrune P
    Eur J Hum Genet; 2005 Mar; 13(3):278-82. PubMed ID: 15586176
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Myoclonus-dystonia due to maternal uniparental disomy.
    Guettard E; Portnoi MF; Lohmann-Hedrich K; Keren B; Rossignol S; Winkler S; El Kamel I; Leu S; Apartis E; Vidailhet M; Klein C; Roze E
    Arch Neurol; 2008 Oct; 65(10):1380-5. PubMed ID: 18852357
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Multistep microsatellite mutation leading to father-child mismatch of FGA locus in a case of non-exclusion parentage.
    Jia YS; Zhang L; Qi LY; Mei K; Zhou FL; Huang DX; Yi SH
    Leg Med (Tokyo); 2015 Sep; 17(5):364-5. PubMed ID: 25979606
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Mosaic maternal uniparental disomy of chromosome 11 in a patient with Silver-Russell syndrome.
    Bullman H; Lever M; Robinson DO; Mackay DJ; Holder SE; Wakeling EL
    J Med Genet; 2008 Jun; 45(6):396-9. PubMed ID: 18474587
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.