These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

150 related articles for article (PubMed ID: 36468027)

  • 21. A dispermic chimera was identified in a healthy man with mixed field agglutination reaction in ABO blood grouping and mosaic 46, XY/46, XX karyotype.
    Hong X; Ying Y; Xu X; Liu Y; Chen Z; Lan X; Ma K; He J; Zhu F; Lv H; Yan L
    Transfus Apher Sci; 2013 Apr; 48(2):223-8. PubMed ID: 23165007
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Clinical and Genetic Analysis of an Infertile Male with 46,XX/46,XY Chimerism.
    Choi EJ; Kim SR; Kim YJ; Kang SM; Kim GY; Kim JH; Lee YJ
    Andrologia; 2019 Apr; 51(3):e13215. PubMed ID: 30536450
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Prenatal diagnosis and normal outcome of a 46,XX/46,XY chimera: a case report.
    Malan V; Gesny R; Morichon-Delvallez N; Aubry MC; Benachi A; Sanlaville D; Turleau C; Bonnefont JP; Fekete-Nihoul C; Vekemans M
    Hum Reprod; 2007 Apr; 22(4):1037-41. PubMed ID: 17272360
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Low-level mosaicism for trisomy 16 at amniocentesis in a pregnancy associated with intrauterine growth restriction and a favorable outcome.
    Chen CP; Chen M; Wang LK; Chern SR; Wu PS; Ma GC; Chang SP; Chen SW; Wu FT; Lee CC; Chen YY; Wang W
    Taiwan J Obstet Gynecol; 2021 Mar; 60(2):345-349. PubMed ID: 33678340
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Blood cell chimerism in dizygotic twins conceived by in vitro fertilization].
    Martos-Moreno GÁ; Campos C; Flores R; Yturriaga R; Pérez-Jurado LA; Argente J
    An Pediatr (Barc); 2013 Oct; 79(4):248-52. PubMed ID: 23726690
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Rare case of XX/XY mosaicism and trisomy 13 in early prenatal diagnosis.
    Sifakis S; Anagnostopoulou K; Plastira K; Vrachnis N; Konstantinidou A; Sklavounou E
    Birth Defects Res A Clin Mol Teratol; 2012 Apr; 94(4):245-8. PubMed ID: 22282126
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Prenatal diagnosis of low-level mosaicism for a small supernumerary marker chromosome derived from chromosome 9q (9q13-q21.33) in a pregnancy with a favorable outcome, and cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes.
    Chen CP; Lo LM; Ko TM; Chern SR; Wu PS; Chen SW; Wu FT; Town DD; Chen LF; Chen YY; Wang W
    Taiwan J Obstet Gynecol; 2021 Mar; 60(2):331-334. PubMed ID: 33678337
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Chimerism resulting from parthenogenetic activation and dispermic fertilization.
    Winberg J; Gustavsson P; Lagerstedt-Robinson K; Blennow E; Lundin J; Iwarsson E; Nordenström A; Anderlid BM; Bondeson ML; Nordenskjöld A; Nordgren A
    Am J Med Genet A; 2010 Sep; 152A(9):2277-86. PubMed ID: 20803645
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Uniparental Disomy in Somatic Mosaicism 45,X/46,XY/46,XX Associated with Ambiguous Genitalia.
    Serra A; Denzer F; Hiort O; Barth TF; Henne-Bruns D; Barbi G; Rettenberger G; Wabitsch M; Just W; Leriche C
    Sex Dev; 2015; 9(3):136-43. PubMed ID: 26043854
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Detection of paternal uniparental disomy 9 in a neonate with prenatally detected mosaicism for a small supernumerary marker chromosome 9 and a supernumerary ring chromosome 9.
    Chen CP; Chen M; Wang LK; Chern SR; Wu PS; Chen SW; Lai ST; Chang SP; Yang CW; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2017 Aug; 56(4):527-533. PubMed ID: 28805612
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A variant Klinefelter syndrome patient with an XXY/XX/XY karyotype studied by GTG-banding and fluorescence in situ hybridization.
    Mark HF; Bai H; Sotomayor E; Mark S; Zolnierz K; Airall E; Sigman M
    Exp Mol Pathol; 1999 Sep; 67(1):50-6. PubMed ID: 10493892
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Analysis of a female with a peripheral blood lymphocytic karyotype of trisomy 18 but normal intelligence].
    Gao J; Yu X; Rong L; Mei B
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Apr; 37(4):483-485. PubMed ID: 32219843
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Prenatal diagnosis of maternal uniparental disomy 21 in association with low-level mosaic trisomy 21 at amniocentesis in a pregnancy associated with intrauterine growth restriction and a favorable outcome.
    Chen CP; Liou JD; Chern SR; Wu PS; Chen SW; Wu FT; Lee MS; Chen YY; Wang W
    Taiwan J Obstet Gynecol; 2022 Jan; 61(1):146-149. PubMed ID: 35181027
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Polymorphic detection of a parthenogenetic maternal and double paternal contribution to a 46,XX/46,XY hermaphrodite.
    Giltay JC; Brunt T; Beemer FA; Wit JM; van Amstel HK; Pearson PL; Wijmenga C
    Am J Hum Genet; 1998 Apr; 62(4):937-40. PubMed ID: 9529354
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Quantitative analysis of chimerism after allogeneic stem cell transplantation by real-time polymerase chain reaction with single nucleotide polymorphisms, standard tandem repeats, and Y-chromosome-specific sequences.
    Koldehoff M; Steckel NK; Hlinka M; Beelen DW; Elmaagacli AH
    Am J Hematol; 2006 Oct; 81(10):735-46. PubMed ID: 16838323
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Prenatal diagnosis and molecular cytogenetic characterization of low-level true mosaicism for trisomy 21 using uncultured amniocytes.
    Chen CP; Wang YL; Chern SR; Wu PS; Chen YN; Chen SW; Chen LF; Lee MS; Yang CW; Wang W
    Taiwan J Obstet Gynecol; 2016 Apr; 55(2):285-7. PubMed ID: 27125416
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Familial ring (18) mosaicism in a 23-year-old young adult with 46,XY,r(18) (::p11→q21::)/46,XY karyotype, intellectual disability, motor retardation and single maxillary incisor and in his phenotypically normal mother, karyotype 47,XX,+r(18)(::p11→q21::)/46,XX.
    Balci S; Tümer C; Karaca C; Bartsch O
    Am J Med Genet A; 2011 May; 155A(5):1129-35. PubMed ID: 21484996
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Mechanisms of mosaicism, chimerism and uniparental disomy identified by single nucleotide polymorphism array analysis.
    Conlin LK; Thiel BD; Bonnemann CG; Medne L; Ernst LM; Zackai EH; Deardorff MA; Krantz ID; Hakonarson H; Spinner NB
    Hum Mol Genet; 2010 Apr; 19(7):1263-75. PubMed ID: 20053666
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 15 in a pregnancy associated with recurrent Down syndrome.
    Chen CP; Chan CH; Chern SR; Wu PS; Chen SW; Wu FT; Town DD; Lee MS; Wang W
    Taiwan J Obstet Gynecol; 2021 Jan; 60(1):152-156. PubMed ID: 33494992
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Prenatal diagnosis of maternal uniparental disomy 16 associated with mosaic trisomy 16 at amniocentesis, and pericardial effusion and intrauterine growth restriction in the fetus.
    Chen CP; Ko TM; Chern SR; Wu PS; Chen SW; Wu FT; Chen YY; Town DD; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2021 May; 60(3):534-539. PubMed ID: 33966743
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.