BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

284 related articles for article (PubMed ID: 21063078)

  • 21. Variability in a family with an insertion involving 5p.
    Marinescu RC; Mamunes P; Kline AD; Schmidt J; Rojas K; Overhauser J
    Am J Med Genet; 1999 Sep; 86(3):258-63. PubMed ID: 10482876
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. Phenotypic and cytogenetic spectrum of 9p trisomy.
    Temtamy SA; Kamel AK; Ismail S; Helmy NA; Aglan MS; El Gammal M; El Ruby M; Mohamed AM
    Genet Couns; 2007; 18(1):29-48. PubMed ID: 17515299
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Hunter-McAlpine craniosynostosis phenotype associated with skeletal anomalies and interstitial deletion of chromosome 17q.
    Thomas JA; Manchester DK; Prescott KE; Milner R; McGavran L; Cohen MM
    Am J Med Genet; 1996 Apr; 62(4):372-5. PubMed ID: 8723067
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Characterization of a complex chromosomal rearrangement in a patient with a typical catlike cry and no other clinical findings of cri-du-chat syndrome.
    Sreekantaiah C; Kronn D; Marinescu RC; Goldin B; Overhauser J
    Am J Med Genet; 1999 Sep; 86(3):264-8. PubMed ID: 10482877
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Cri du chat mosaicism: an unusual case of partial deletion and partial deletion/ duplication of the short arm of chromosome 5, leading to an unusual cri du chat phenotype.
    Murru D; Boccone L; Ristaldi MS; Nucaro AL
    Genet Couns; 2008; 19(4):381-6. PubMed ID: 19239081
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Molecular and cytogenetic characterization of 9p- abnormalities.
    Teebi AS; Gibson L; McGrath J; Meyn MS; Breg WR; Yang-Feng TL
    Am J Med Genet; 1993 May; 46(3):288-92. PubMed ID: 8488873
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Cri du chat-syndrome in combination with partial trisomy 9 p.
    Sigmund J; Frisch H; Heinz-Erian P; Rhomberg K; Wegner RD
    Padiatr Padol; 1986; 21(1):61-7. PubMed ID: 3960564
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Delineation of the dup5q phenotype by molecular cytogenetic analysis in a patient with dup5q/del 5p (cri du chat).
    Levy B; Dunn TM; Kern JH; Hirschhorn K; Kardon NB
    Am J Med Genet; 2002 Mar; 108(3):192-7. PubMed ID: 11891684
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Paternally originated Wolf-Hirschhorn syndrome detected by multiplex ligation-dependent probe amplification and microarray comparative genomic hybridization].
    Zhu CJ; Huang ZY; Wu WQ; Zhao Q; Jiang HY; Xie JS
    Zhonghua Er Ke Za Zhi; 2012 Jun; 50(6):460-4. PubMed ID: 22931946
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Genitourinary phenotype in XX patients with distal 9p monosomy.
    Fujimoto Y; Okuyama T; Iijima M; Tanaka T; Horikawa R; Yamada K; Ogata T
    Mol Genet Metab; 2004 Jun; 82(2):173-9. PubMed ID: 15172006
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Partial trisomy 1p (1p36.22-->pter) and partial monosomy 9p (9p22.2-->pter) associated with achalasia, flexion deformity of the fingers and epilepsy in a girl.
    Chen CP; Lin SP; Lee CC; Town DD; Wang W
    Genet Couns; 2006; 17(3):301-6. PubMed ID: 17100198
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Localization by FISH of centric fission breakpoints in a de novo trisomy 9p patient with i(9p) and t(9q;11p).
    Petit P; Devriendt K; Vermeesch JR; Meireleire J; Fryns JP
    Genet Couns; 1998; 9(3):215-21. PubMed ID: 9777345
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Characterization of a Complex Chromosomal Rearrangement Involving a de novo Duplication of 9p and 9q and a Deletion of 9q.
    Martín-De Saro MD; Valdés-Miranda JM; Plaza-Benhumea L; Pérez-Cabrera A; Gonzalez-Huerta LM; Guevara-Yañez R; Cuevas-Covarrubias SA
    Cytogenet Genome Res; 2015; 147(2-3):124-9. PubMed ID: 26900692
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Phenotype positioning on chromosomes in a patient with the syndrome of partial trisomy 7p21.2-->pter].
    Liang DS; Wu LQ; Cai F; Xia K; Long ZG; Pan Q; Dai HP; Xia JH
    Yi Chuan Xue Bao; 2005 Feb; 32(2):124-9. PubMed ID: 15759858
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Tandem duplication/deletion in a maternally derived chromosome 9 supernumerary derivative resulting in 9p trisomy and partial 9q tetrasomy.
    Wyandt HE; Lebo RV; Fenerci EY; Sadhu DN; Milunsky JM
    Am J Med Genet; 2000 Aug; 93(4):305-12. PubMed ID: 10946358
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Directly inherited partial trisomy of chromosome 6p identified in a father and daughter by chromosome microdissection.
    Delatycki MB; Voullaire L; Francis D; Petrovic V; Robertson A; Webber LM; Slater HR
    J Med Genet; 1999 Apr; 36(4):335-8. PubMed ID: 10227406
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Prenatal diagnosis and molecular cytogenetic characterization of a de novo unbalanced reciprocal translocation of der(9)t(9;14)(p24.2;q32.11) associated with 9p terminal deletion and 14q distal duplication.
    Chen CP; Lin CJ; Chern SR; Wu PS; Chen YN; Chen SW; Lee CC; Chen LF; Yang CW; Wang W
    Taiwan J Obstet Gynecol; 2016 Aug; 55(4):596-601. PubMed ID: 27590390
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. Case report. Familial balanced translocation leading to an offspring with phenotypic manifestations of 9p syndrome.
    Abreu LS; Brassesco MS; Moreira ML; Pina-Neto JM
    Genet Mol Res; 2014 Jun; 13(2):4302-10. PubMed ID: 25036174
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 15.