BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

153 related articles for article (PubMed ID: 15057986)

  • 1. Phenotypical variation in cousins with the identical partial trisomy 9 (pter-q22.2) and 7 (q35-qter) at 16 and 23 weeks gestation.
    Metzke-Heidemann S; Kuhling-von Kaisenberg H; Caliebe A; Janssen D; Jonat W; Grote W; von Kaisenberg CS
    Am J Med Genet A; 2004 Apr; 126A(2):197-203. PubMed ID: 15057986
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Absence of 9q22-9qter in trisomy 9 does not prevent a Dandy-Walker phenotype.
    von Kaisenberg CS; Caliebe A; Krams M; Hackelöer BJ; Jonat W
    Am J Med Genet; 2000 Dec; 95(5):425-8. PubMed ID: 11146460
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Complete trisomy 9 with unusual phenotypic associations: Dandy-Walker malformation, cleft lip and cleft palate, cardiovascular abnormalities.
    Tonni G; Lituania M; Chitayat D; Bonasoni MP; Keating S; Thompson M; Shannon P
    Taiwan J Obstet Gynecol; 2014 Dec; 53(4):592-7. PubMed ID: 25510707
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A child with multiple congenital anomalies due to partial trisomy 7q22.1 → qter resulting from a maternally inherited balanced translocation: a case report and review of literature.
    Paththinige CS; Sirisena ND; Kariyawasam UGIU; Ediriweera RC; Kruszka P; Muenke M; Dissanayake VHW
    BMC Med Genomics; 2018 May; 11(1):44. PubMed ID: 29739404
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prenatal diagnosis of the Dandy-Walker malformation and ventriculomegaly associated with partial trisomy 9p and distal 12p deletion.
    Chen CP; Chang TY; Shih JC; Lin SP; Lin CJ; Wang W; Lee CC; Town DD; Pan CW; Tzen CY
    Prenat Diagn; 2002 Dec; 22(12):1063-6. PubMed ID: 12454959
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Partial trisomy 2q(2q37.3-->qter) and monosomy 7q(7q34--->qter) due to paternal reciprocal translocation 2;7: a case report.
    Ahn JM; Koo DH; Kwon KW; Lee YK; Lee YH; Lee HH; Nam KH; Lee KH
    J Korean Med Sci; 2003 Feb; 18(1):112-3. PubMed ID: 12589098
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Prenatal diagnosis of a fetus with partial monosomy 7(q34-->qter) and partial trisomy 18(q21-->qter).
    Pluchon E; Giovangrandi Y; Labbe F; Le Bris MJ; Collet M; Brettes JP; Riviere D; Riviere MR
    Prenat Diagn; 1993 Oct; 13(10):983-8. PubMed ID: 8309904
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Unbalanced translocation 6p/16q (partial monosomy 6p and trisomy 16q): prenatal diagnosis and cytogenetics.
    Puhl AG; Zelazny J; Galetzka D; Skala C; Frey-Mahn G; Wellek B; Koelbl H
    Eur J Obstet Gynecol Reprod Biol; 2010 Jun; 150(2):119-25. PubMed ID: 20211513
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 7p (7p15.3→pter) and partial monosomy 13q (13q33.3→qter) associated with Dandy-Walker malformation, abnormal skull development and microcephaly.
    Chen CP; Chen M; Su YN; Tsai FJ; Chern SR; Hsu CY; Wu PC; Town DD; Lee DJ; Ma GC; Wang W
    Taiwan J Obstet Gynecol; 2010 Sep; 49(3):320-6. PubMed ID: 21056318
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Ultrasound diagnosis of central nervous system anomalies (bifid choroid plexus, ventriculomegaly, Dandy-Walker malformation) associated with multicystic dysplastic kidney disease in a trisomy 9 fetus: case report with literature review.
    Tonni G; Grisolia G
    J Clin Ultrasound; 2013 Sep; 41(7):441-7. PubMed ID: 23055272
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Partial trisomy 3q syndrome inherited from familial t(3;9)(q26.1; p23).
    Tranebjaerg L; Baekmark UB; Dyhr-Nielsen M; Kreiborg S
    Clin Genet; 1987 Aug; 32(2):137-43. PubMed ID: 3652493
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prenatal diagnosis of supernumerary der(22)t(11;22) associated with the Dandy-Walker malformation in a fetus.
    Chen CP; Liu FF; Jan SW; Yang YC; Lan CC
    Prenat Diagn; 1996 Dec; 16(12):1137-40. PubMed ID: 8994250
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Trisomy 4p in four relatives: variability and lack of distinctive features in phenotypic expression.
    Reynolds JF; Shires MA; Wyandt HE; Kelly TE
    Clin Genet; 1983 Nov; 24(5):365-74. PubMed ID: 6418421
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Chromosomal 10Q26 trisomy resulting from paternal T(9;10)(PTER;Q26.1).
    Hou JW
    J Formos Med Assoc; 2003 Dec; 102(12):887-92. PubMed ID: 14976570
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Variable expression of phenotype in offspring with partial monosomy 7q and partial trisomy 8p in a family with a rcp (7;8)(134;p12) translocation.
    Frints SG; Moerman P; Fryns JP
    Genet Couns; 1996; 7(4):313-9. PubMed ID: 8985736
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prenatal diagnosis and molecular cytogenetics in a case of partial trisomy 14 and monosomy 21.
    Lee C; Fowler DJ; Lemyre E; Sandstrom MM; Holmes LB; Morton CC
    Am J Med Genet; 2001 May; 100(3):246-50. PubMed ID: 11343311
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Partial trisomy 16q21➔qter due to an unbalanced segregation of a maternally inherited balanced translocation 46,XX,t(15;16)(p13;q21): a case report and review of literature.
    Mishra R; Paththinige CS; Sirisena ND; Nanayakkara S; Kariyawasam UGIU; Dissanayake VHW
    BMC Pediatr; 2018 Jan; 18(1):4. PubMed ID: 29310616
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The phenotype of partial dup(7q) reconsidered: a report of five new cases.
    Forabosco A; Baroncini A; Dalpra L; Chessa L; Giannotti A; Maccagnani F; Dallapiccola B
    Clin Genet; 1988 Jul; 34(1):48-59. PubMed ID: 3409538
    [TBL] [Abstract][Full Text] [Related]  

  • 20. High risk for unbalanced segregation of some reciprocal translocations: a large pedigree containing distal 4q trisomy from t(4;7)(q28;p22).
    Francisco-Bagnariolli AM; Payão SL; Kawasaki-Oyama RS; Sabbag Filho D; Segato R; de Labio RW; Chauffaille ML; Priest JH
    Am J Med Genet; 2001 Nov; 103(4):302-7. PubMed ID: 11746010
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.