BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

663 related articles for article (PubMed ID: 9412788)

  • 21. Partial trisomy 1p due to paternal t(1;9) translocation in a family with recurrent miscarriages.
    Demirhan O; Tastemir D
    Fertil Steril; 2006 Jul; 86(1):219.e15-9. PubMed ID: 16818035
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Familial reciprocal translocation t(7;16) associated with maternal uniparental disomy 7 in a Silver-Russell patient.
    Dupont JM; Cuisset L; Cartigny M; Le Tessier D; Vasseur C; Rabineau D; Jeanpierre M
    Am J Med Genet; 2002 Sep; 111(4):405-8. PubMed ID: 12210300
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Maternal uniparental disomy for chromosome 14 in a boy with intrauterine growth retardation.
    Miyoshi O; Hayashi S; Fujimoto M; Tomita H; Sohda M; Niikawa N
    J Hum Genet; 1998; 43(2):138-42. PubMed ID: 9621521
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Two cases of partial trisomy 10q syndrome due to a familial 10;20 translocation.
    Tüysüz B; Hacihanefioglu S; Silahtaroglu A; Yilmaz S; Deviren A; Cenani A
    Genet Couns; 2000; 11(4):355-61. PubMed ID: 11140413
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Maternal uniparental disomy 16 and genetic counseling: new case and survey of published cases.
    Eggermann T; Curtis M; Zerres K; Hughes HE
    Genet Couns; 2004; 15(2):183-90. PubMed ID: 15287418
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Tetrasomy 5p mosaicism in a boy with delayed growth, hypotonia, minor anomalies, and an additional isochromosome 5p [46,XY/47,XY, + i(5p)].
    Sijmons RH; Leegte B; van Lingen RA; de Pater JM; van der Veen AY; del Canho H; Bos C; ten Kate LP; Breed AS
    Am J Med Genet; 1993 Sep; 47(4):559-62. PubMed ID: 7504882
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Partial trisomy 6p from a de novo translocation (6;18) with variable mosaicism in different tissues.
    Rudnik-Schöneborn S; Schubert R; Majewski F; Haverkamp F; Schwanitz G
    Clin Genet; 1997 Aug; 52(2):126-9. PubMed ID: 9298749
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Monozygotic twins discordant for partial trisomy 1.
    Watson WJ; Katz VL; Albright SG; Rao KW; Aylsworth AS
    Obstet Gynecol; 1990 Nov; 76(5 Pt 2):949-51. PubMed ID: 2216262
    [TBL] [Abstract][Full Text] [Related]  

  • 29. ["De novo" partial trisomy 16p (author's transl)].
    Gabarrón Llamas J; Cabrerizo Portero D; Montserrat Bernal F; Rodríguez Costa T; Cabrerizo Merino C; Rodríguez López F
    An Esp Pediatr; 1981 Dec; 15(6):587-91. PubMed ID: 7337311
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Cytogenetic and age-dependent risk factors associated with uniparental disomy 15.
    Robinson WP; Langlois S; Schuffenhauer S; Horsthemke B; Michaelis RC; Christian S; Ledbetter DH; Schinzel A
    Prenat Diagn; 1996 Sep; 16(9):837-44. PubMed ID: 8905898
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Uniparental disomy with and without confined placental mosaicism: a model for trisomic zygote rescue.
    Los FJ; van Opstal D; van den Berg C; Braat AP; Verhoef S; Wesby-van Swaay E; van den Ouweland AM; Halley DJ
    Prenat Diagn; 1998 Jul; 18(7):659-68. PubMed ID: 9706646
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Non-mosaic trisomy 16 in a third-trimester fetus.
    Yancey MK; Hardin EL; Pacheco C; Kuslich CD; Donlon TA
    Obstet Gynecol; 1996 May; 87(5 Pt 2):856-60. PubMed ID: 8677115
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Mosaic 13 trisomy due to de novo 13/13 translocation with subsequent fission. Karyotype: 46,XX,-13, +t(13;13)(p11;q11)/46,XX,del(13)(p11). A second example.
    Fryns JP; Kleczkowska A; Jaeken J; Van Herck K; Van den Berghe MH
    Ann Genet; 1989; 32(3):177-9. PubMed ID: 2486064
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Unusual mosaic trisomy 13 through 13/13 translocation and monosomy 13 with a small ring.
    Jalal SM; Martin JA; Benjamin TR; Kukolich MK; Townsend-Parcham JK
    Ann Genet; 1990; 33(3):173-5. PubMed ID: 2288463
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Trisomy 16pter to 16q12.1 and monosomy 22pter to 22q11.2 resulting from adjacent-2 segregation of a maternal complex chromosome rearrangement.
    Xu J; Chernos J; Roland B
    Am J Med Genet; 1997 Dec; 73(3):327-9. PubMed ID: 9415693
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Trisomy 6q22 leads to 6qter due to maternal 6;21 translocation. Case report review of the literature.
    Taysi K; Chao WT; Monaghan N; Monaco MP
    Ann Genet; 1983; 26(4):243-6. PubMed ID: 6364954
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Uniparental disomy: a review of causes and clinical sequelae].
    Engel E
    Ann Genet; 1995; 38(3):113-36. PubMed ID: 8540683
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Abnormal phenotypes in uniparental disomy (UPD): fundamental aspects and a critical review with bibliography of UPD other than 15.
    Kotzot D
    Am J Med Genet; 1999 Jan; 82(3):265-74. PubMed ID: 10215553
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Clinical and molecular cytogenetic studies in a case with partial trisomy 12p due to a de novo supernumerary ring chromosome.
    Ausems MG; Schuil J; Van Raveswaaij-Arts C; De Pater JM
    Genet Couns; 2004; 15(4):405-10. PubMed ID: 15658615
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Paternal meiotic origin of der(21;21)(q10;q10) mosaicism [46,XX/46, XX,der(21;21)(q10;q10),+21] in a girl with mild Down syndrome.
    Kotzot D; Schinzel A
    Eur J Hum Genet; 2000 Sep; 8(9):709-12. PubMed ID: 10980577
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 34.