BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

157 related articles for article (PubMed ID: 19039519)

  • 1. Phenotypical manifestations of partial trisomy 9 and monosomy 4 in two siblings.
    Vanlandingham M; Nguyen TV; Abdul-Rahman OA; Parent A; Zhang J
    Neurol Sci; 2008 Dec; 29(6):467-70. PubMed ID: 19039519
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Two siblings with partial trisomy 15 and monosomy 21 associated with central nervous system anomalies.
    Ishida A; Sawaishi Y; Goto A; Takahashi Y; Arai H; Nakajima W; Onozaki M; Takada G
    Tohoku J Exp Med; 1993 Dec; 171(4):277-83. PubMed ID: 8184402
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Outcomes of two different unbalanced segregations from a maternal t(4;10)(q33;p15.1) translocation.
    Fan J; Senaratne TN; Liu JY; Bina M; Martinez-Agosto JA; Quintero-Rivera F; Wang JJ
    BMC Med Genomics; 2023 Mar; 16(1):65. PubMed ID: 36991446
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Partial monosomy 10q and partial trisomy 9q with anal atresia due to maternal translocation: t(9;10)(q32;q26).
    Tsukuda T; Nagata I; Sawada H; Murakami J; Hanaki K; Urashima H; Kaneda T; Shimizu N; Kaibara N; Kodama N; Ohzeki T; Shiraki K
    Clin Genet; 1996 Oct; 50(4):220-2. PubMed ID: 9001803
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Partial trisomy 4q and partial monosomy 9p in a girl with choanal atresia and various dysmorphic findings.
    Cakmak-Genc G; Karakas-Celik S; Dursun A; Piskin İE
    Gene; 2015 Sep; 568(2):211-4. PubMed ID: 25979671
    [TBL] [Abstract][Full Text] [Related]  

  • 6. An unusual clinical characterization of a male with distal partial trisomy 1q42.1 and monosomy 4q35.1 and review of the literature.
    Wang CB; Lin SP; Chen CP; Chen YJ; Lee CC
    Genet Couns; 2006; 17(4):435-40. PubMed ID: 17375530
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Partial trisomy and partial monosomy of the distal long arm of chromosome 4: patient report and literature review.
    Frints SG; Schrander-Stumpel CT; Engelen JJ; Da Costa AJ; Fryns JP
    Genet Couns; 1996; 7(2):135-42. PubMed ID: 8831133
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Segregation of a paternal insertional translocation results in partial 4q monosomy or 4q trisomy in two siblings.
    Hegmann KM; Spikes AS; Orr-Urtreger A; Shaffer LG
    Am J Med Genet; 1996 Jan; 61(1):10-5. PubMed ID: 8741910
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Case report of newborn with de novo partial trisomy 2q31.2-37.3 and monosomy 9p24.3.
    Colangelo M; Alfonsi M; Palka C; Zio EZ; Renzo SD; Guanciali-Franchi P; Palka G
    J Genet; 2018 Mar; 97(1):311-317. PubMed ID: 29666350
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Partial trisomy and partial monosomy resulting from a reciprocal segregating in a large family.
    Velagaleti GV; Hawkins JC; Panova NI; Lockhart LH
    Indian J Pediatr; 2008 Sep; 75(9):956-60. PubMed ID: 18568304
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Partial trisomy 4q and monosomy 9p resulting from a familial translocation t(4;9)(q27;p24) in a child with choanal atresia.
    Wouters CH; van Bodegom TM; Moll HA; Govaerts LC
    Ann Genet; 1999; 42(3):160-5. PubMed ID: 10526659
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Isolated myocardial non-compaction in an infant with distal 4q trisomy and distal 1q monosomy.
    De Rosa G; Pardeo M; Bria S; Caresta E; Vasta I; Zampino G; Zollino M; Zuppa AA; Piastra M
    Eur J Pediatr; 2005 Apr; 164(4):255-6. PubMed ID: 15666158
    [No Abstract]   [Full Text] [Related]  

  • 13. Partial trisomy of the long arm of chromosome 1: prenatal diagnosis, clinical evaluation and cytogenetic findings. Case report and review of the literature.
    Cambosu F; Capobianco G; Fogu G; Bandiera P; Pirino A; Moro MA; Sanna R; Soro G; Dessole M; Montella A
    J Obstet Gynaecol Res; 2013 Feb; 39(2):592-7. PubMed ID: 22925348
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mild phenotype in two siblings with distal monosomy 12p13.31-->pter.
    Glass IA; Trenholme A; Mildenhall L; Bailey RJ; Cotter PD
    Clin Genet; 2000 May; 57(5):401-5. PubMed ID: 10852377
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Blepharophimosis and mental retardation (BMR) phenotypes caused by chromosomal rearrangements: description in a boy with partial trisomy 10q and monosomy 4q and review of the literature.
    Bartholdi D; Toelle SP; Steiner B; Boltshauser E; Schinzel A; Riegel M
    Eur J Med Genet; 2008; 51(2):113-23. PubMed ID: 18262484
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A 14-year follow-up of a case detected prenatally of partial trisomy 13q21.32-qter and monosomy 18q22.3-qter as a result of a maternal complex chromosome rearrangement involving chromosomes 6, 13, and 18.
    Quadrelli R; Quadrelli A; Milunsky A; Zou YS; Huang XL; Viera E; Mechoso B; Bellini S; Costabel M; Vaglio A
    Genet Test Mol Biomarkers; 2009 Jun; 13(3):387-93. PubMed ID: 19473082
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Subtelomeric 6p monosomy and 12q trisomy in a patient with a 46,XX,der(6)t(6;12)(p25.3;q24.31) karyotype: Phenotypic overlap with Mutchinick syndrome.
    Semerci CN; Cinbis M; Ullmann R; Steininger A; Bahce M; Yagci B; Ozden S; Sabir N; Gumus D; Tepeli E; Arteaga J; Mutchinick OM
    Am J Med Genet A; 2010 Jul; 152A(7):1724-9. PubMed ID: 20578131
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Partial monosomy 2p and partial trisomy 4q due to paternal translocation t(2;4)(p25.1;q31.3).
    Skrlec I; Wagner J; Puseljić S; Heffer M; Stipoljev F
    Coll Antropol; 2014 Jun; 38(2):759-62. PubMed ID: 25145019
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Partial monosomy 8q and partial trisomy 9q due to the maternal translocation t(8;9(q24.3;q34.1): a case report.
    Tos T; Alp MY; Eker HK; Cebi AH; Ikbal M
    Genet Couns; 2014; 25(1):35-9. PubMed ID: 24783653
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.