BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

212 related articles for article (PubMed ID: 12833408)

  • 1. Newborn with malformations and a combined duplication of 9pter-q22 and 16q22-qter resulting from unbalanced segregation of a complex maternal translocation.
    Piram A; Ortolan D; Peres LC; Pina-Neto JM; Riegel M; Schinzel A
    Am J Med Genet A; 2003 Jul; 120A(2):247-52. PubMed ID: 12833408
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Phenotypic features of a boy with trisomy of 16q22-->qter due to paternal Y; 16 translocation.
    Tsien F; Morava E; Talarski A; Marble M
    Clin Dysmorphol; 2005 Oct; 14(4):177-181. PubMed ID: 16155418
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Double partial trisomy 9q34.1-->qter and 21pter-->q22.11: FISH and clinical findings.
    Mattina T; Pierluigi M; Mazzone D; Scardilli S; Perfumo C; Mollica F
    J Med Genet; 1997 Nov; 34(11):945-8. PubMed ID: 9391894
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A severely mental and motor retarded boy with monosomy 9pter-->p22 trisomy 10q26-->qter due to paternal reciprocal translocation 46,XY,t(9;10)(p23;q26).
    Akbas E; Polat S; Karakas-Celik S; Altintas ZM; Yildirim M; Yilgor E
    Genet Couns; 2011; 22(4):417-23. PubMed ID: 22303803
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Double partial trisomy of 6p23-pter and 9pter-q21.2 in a neonate resulting from 4:2 meiotic segregation of a maternal complex t(6;7;9)(p23;p15;q21.2) translocation.
    Cetin Z; Mihci E; Keser I; Karaali K; Berker S; Luleci G
    Genet Couns; 2012; 23(2):239-47. PubMed ID: 22876583
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Translocation/duplication of 9p onto a duplicated 4q.
    Rivera H; Figuera LE; Vasquez AI
    Genet Couns; 1992; 3(4):201-3. PubMed ID: 1472355
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Familial translocation t(9;16).
    Dowman C; Lockwood D; Allanson J
    J Med Genet; 1989 Aug; 26(8):525-8. PubMed ID: 2671373
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Duplication of 16q22-->qter confirmed by fluorescence in situ hybridisation and molecular analysis.
    Houlston RS; Renshaw RM; James RS; Ironton R; Temple IK
    J Med Genet; 1994 Nov; 31(11):884-7. PubMed ID: 7853376
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Cytogenetic analysis of partial trisomy 9p resulting from a reciprocal balanced 9/21 translocation].
    Wang XR; Luo RL; Dai XH; Liu JY
    Yi Chuan; 2007 Jul; 29(7):813-6. PubMed ID: 17646146
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Trisomy 16q21 --> qter: Seven-year follow-up of a girl with unusually long survival.
    de Carvalho AF; da Silva Bellucco FT; dos Santos NP; Pellegrino R; de Azevedo Moreira LM; Toralles MB; Kulikowski LD; Melaragno MI
    Am J Med Genet A; 2010 Aug; 152A(8):2074-8. PubMed ID: 20635361
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Perinatal findings and molecular cytogenetic analysis of de novo partial trisomy 16q (16q22.1-->qter) and partial monosomy 20q (20q13.3-->qter).
    Chen CP; Lin SP; Lin CC; Li YC; Chern SR; Chen WM; Lee CC; Hsieh LJ; Wang W
    Prenat Diagn; 2005 Feb; 25(2):112-8. PubMed ID: 15712324
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Partial trisomy 1q41-qter and partial trisomy 9pter-9q21.32 in a newborn infant: an array CGH analysis and review.
    Akalin I; Bozdag S; Spielmann M; Basaran SY; Nanda I; Klopocki E
    Am J Med Genet A; 2014 Feb; 164A(2):490-4. PubMed ID: 24311106
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Prenatal findings and molecular cytogenetic analyses of partial trisomy 12q (12q24.32-->qter) and partial monosomy 21q (21q22.2-->qter).
    Chen CP; Chern SR; Lin CC; Wang TH; Li YC; Hsieh LJ; Lee CC; Hua HM; Wang W
    Prenat Diagn; 2006 Apr; 26(4):313-20. PubMed ID: 16506269
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Partial duplication 16p resulting from a 3:1 segregation of a maternal reciprocal translocation.
    Mori MA; Gomar JL; Diaz de Bustamante A; Ananias A; Pinel I; Martinez-Frias ML
    Am J Med Genet; 1987 Jan; 26(1):203-6. PubMed ID: 3812563
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Adjacent-2 disjunction of a maternal t(9;22) leading to duplication 9pter----q22 and deficiency of 22pter----q11.2.
    Pivnick EK; Wilroy RS; Summitt JB; Tucker B; Herrod HG; Tharapel AT
    Am J Med Genet; 1990 Sep; 37(1):92-6. PubMed ID: 2240050
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Pure 9p trisomy derived from a terminal balanced unreciprocal translocation.
    Brambila-Tapia AJ; Neira VA; Vásquez-Velásquez AI; Jimenez-Arredondo RE; Chávez-González EL; Picos-Cárdenas VJ; Fletes-Rayas AL; Figuera LE
    Genet Couns; 2014; 25(3):289-97. PubMed ID: 25365851
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Duplication 11 (q22----qter) in an infant. A case report with review.
    Greig F; Rosenfeld W; Verma RS; Babu KA; David K
    Ann Genet; 1985; 28(3):185-8. PubMed ID: 3879155
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.