BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

874 related articles for article (PubMed ID: 16719278)

  • 21. Molecular characterization of partial trisomy 16q24.1-qter: clinical report and review of the literature.
    Brisset S; Joly G; Ozilou C; Lapierre JM; Gosset P; LeLorc'h M; Raoul O; Turleau C; Vekemans M; Romana SP
    Am J Med Genet; 2002 Dec; 113(4):339-45. PubMed ID: 12457405
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Two cases of 9p deletion syndrome and a case of partial trisomy 8 and partial monosomy 9p.
    Okten G; Sezer O; Günes S; Küçüködük S; Oğur G
    Genet Couns; 2009; 20(4):341-7. PubMed ID: 20162869
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. Characterization of a derivative chromosome 17 by fish-technique.
    Ramesh KH; Shah HO; Sherman J; Lin JH; Verma RS
    Ann Genet; 1996; 39(3):177-80. PubMed ID: 8839891
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Prenatal diagnosis of partial trisomy 3p(3p23-->pter) and monosomy 7q(7q36-->qter) in a fetus with microcephaly alobar holoprosencephaly and cyclopia.
    Chen CP; Devriendt K; Lee CC; Chen WL; Wang W; Wang TY
    Prenat Diagn; 1999 Oct; 19(10):986-9. PubMed ID: 10521829
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Prenatal diagnosis of partial monosomy 18p(18p11.2-->pter) and trisomy 21q(21q22.3-->qter) with alobar holoprosencephaly and premaxillary agenesis.
    Chen CP; Chern SR; Wang W; Lee CC; Chen WL; Chen LF; Chang TY; Tzen CY
    Prenat Diagn; 2001 May; 21(5):346-50. PubMed ID: 11360273
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Severe upper airway stenosis in a boy with partial monosomy 16p13.3pter and partial trisomy 16q22qter.
    Yamada K; Uchiyama A; Arai M; Kubodera K; Yamamoto Y; Orii KO; Nagasawa H; Masuno M; Kohno Y
    Congenit Anom (Kyoto); 2009 Jun; 49(2):85-8. PubMed ID: 19489960
    [TBL] [Abstract][Full Text] [Related]  

  • 28. True telomeric translocation in a baby with the Prader-Willi phenotype.
    Reeve A; Norman A; Sinclair P; Whittington-Smith R; Hamey Y; Donnai D; Read A
    Am J Med Genet; 1993 Aug; 47(1):1-6. PubMed ID: 8368237
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Prenatal diagnosis of a fetus affected with Down syndrome and deletion 1p36 syndrome by fluorescence in situ hybridization and spectral karyotyping.
    Hsieh LJ; Hsieh TC; Yeh GP; Lin MI; Chen M; Wang BB
    Fetal Diagn Ther; 2004; 19(4):356-60. PubMed ID: 15192296
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A de novo subtelomeric monosomy 11q (11q24.2-qter) and trisomy 20q (20q13.3-qter) in a girl with findings compatible with Jacobsen syndrome: case report and review.
    Courtens W; Wauters J; Wojciechowski M; Reyniers E; Scheers S; van Luijk R; Rooms L; Kooy F; Wuyts W
    Clin Dysmorphol; 2007 Oct; 16(4):231-9. PubMed ID: 17786114
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Partial 6q monosomy/partial 12q trisomy in a child with features of Kabuki make-up syndrome.
    Jardine PE; Burvill-Holmes LC; Schutt WH; Lunt PW
    Clin Dysmorphol; 1993 Jul; 2(3):269-73. PubMed ID: 8287190
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A severely mentally and motor retarded girl with monosomy 3pter-->p25 and trisomy 8q24-->qter due to a familial reciprocal translocation t(3;8)(p25;q24).
    Balci S; Aypar E; Beksaç MS; Bartsch O
    Genet Couns; 2009; 20(2):125-32. PubMed ID: 19650409
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Congenital glaucoma and Silver-Russell phenotype associated with partial trisomy 7q and monosomy 15q.
    Kato R; Kishibayashi J; Shimokawa O; Harada N; Niikawa N; Matsumoto N
    Am J Med Genet; 2001 Dec; 104(4):319-22. PubMed ID: 11754068
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Partial trisomy 13q identified by sequential fluorescence in situ hybridization.
    Rao VV; Carpenter NJ; Gucsavas M; Coldwell J; Say B
    Am J Med Genet; 1995 Jul; 58(1):50-3. PubMed ID: 7573156
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Cytogenetic and molecular studies of an X;21 translocation previously diagnosed as complete monosomy 21.
    Cardoso LC; Moraes L; Camilo MJ; Mulatinho MV; Ramos H; Almeida JC; Llerena JC; Seuánez HN; Vargas FR
    Eur J Med Genet; 2008; 51(6):588-97. PubMed ID: 18674646
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Beckwith-Wiedemann syndrome due to 11p15.5 paternal duplication associated with Klinefelter syndrome and a "de novo" pericentric inversion of chromosome Y.
    Delicado A; Lapunzina P; Palomares M; Molina MA; Galán E; López Pajares I
    Eur J Med Genet; 2005; 48(2):159-66. PubMed ID: 16053907
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Two cousins with partial trisomy 12q and monosomy 12p recombinants of a familial pericentric inversion of the chromosome 12.
    Lagier-Tourenne C; Ginglinger E; Alembik Y; De Saint Martin A; Peter MO; Dulucq P; Jonveaux P; Jeandidier E
    Am J Med Genet A; 2004 Feb; 125A(1):77-85. PubMed ID: 14755471
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Untreated growth hormone deficiency with extremely short stature, bone dysplasia, cleft lip--palate and severe mental retardation in a 26-year-old man with a de novo unbalanced translocation t(1;12)(q24;q24).
    Callier P; Faivre L; Marle N; Thauvin-Robinet C; Mosca AL; Masurel-Paulet A; Borgnon J; Falcon-Eicher S; Danino A; Malka G; Le Merrer M; Huet F; Mugneret F
    Eur J Med Genet; 2007; 50(6):455-64. PubMed ID: 17720646
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Prenatal diagnosis of a micropenis in a male fetus with partial trisomy 12q (12q24.32-->qter) and partial monosomy 21q (21q22.2-->ter-->qter).
    Chen CP; Lin CC; Chang TY; Li YC; Hsieh LJ; Lee CC; Chen LF; Wang W
    Prenat Diagn; 2006 Aug; 26(8):757-9. PubMed ID: 16865745
    [No Abstract]   [Full Text] [Related]  

  • 40. Partial trisomy of the distal part of 10q: a report of two Egyptian cases.
    Aglan MS; Kamel AK; Helmy NA
    Genet Couns; 2008; 19(2):199-209. PubMed ID: 18618995
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 44.