BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

142 related articles for article (PubMed ID: 11754065)

  • 1. Two inv dup(15) chromosomes in a woman with repeated abortions.
    Shim SH; Lee CH; Park YJ; Lee HJ; Park WI; Cho YH
    Am J Med Genet; 2001 Dec; 104(4):303-6. PubMed ID: 11754065
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Refined molecular characterization of the breakpoints in small inv dup(15) chromosomes.
    Huang B; Crolla JA; Christian SL; Wolf-Ledbetter ME; Macha ME; Papenhausen PN; Ledbetter DH
    Hum Genet; 1997 Jan; 99(1):11-7. PubMed ID: 9003485
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Unusual features in children with inv dup(15) supernumerary marker: a study of genotype-phenotype correlation in Taiwan.
    Hou JW; Wang TR
    Eur J Pediatr; 1998 Feb; 157(2):122-7. PubMed ID: 9504785
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Supernumerary inv dup(15) in a patient with Angelman syndrome and a deletion of 15q11-q13.
    Spinner NB; Zackai E; Cheng SD; Knoll JH
    Am J Med Genet; 1995 May; 57(1):61-5. PubMed ID: 7645601
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The inv dup (15) or idic (15) syndrome (Tetrasomy 15q).
    Battaglia A
    Orphanet J Rare Dis; 2008 Nov; 3():30. PubMed ID: 19019226
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Molecular cytogenetic characterization of an inv dup(15) chromosome presenting as a small supernumerary marker chromosome associated with the inv dup(15) syndrome.
    Chen CP; Lin SP; Chern SR; Wu PS; Chen YN; Chen SW; Lee CC; Town DD; Yang CW; Wang W
    Taiwan J Obstet Gynecol; 2016 Oct; 55(5):728-732. PubMed ID: 27751425
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Infertility and marker chromosomes: application of molecular cytogenetic techniques in a case of inv dup(15).
    Vulcani-Freitas TM; Gil-da-Silva-Lopes VL; Varella-Garcia M; Maciel-Guerra AT
    J Appl Genet; 2006; 47(1):89-91. PubMed ID: 16424615
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mild generalized epilepsy and developmental disorder associated with large inv dup(15).
    Chifari R; Guerrini R; Pierluigi M; Cavani S; Sgrò V; Elia M; Canger R; Canevini MP
    Epilepsia; 2002 Sep; 43(9):1096-100. PubMed ID: 12199736
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Simultaneous formation of inv dup(15) and dup(15q) in a girl with developmental delay: origin of the abnormal chromosomes.
    Abeliovich D; Dagan J; Werner M; Lerer I; Shapira Y; Meiner V
    Eur J Hum Genet; 1995; 3(1):49-55. PubMed ID: 7767656
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular cytogenetic analysis of inv dup(15) chromosomes, using probes specific for the Prader-Willi/Angelman syndrome region: clinical implications.
    Leana-Cox J; Jenkins L; Palmer CG; Plattner R; Sheppard L; Flejter WL; Zackowski J; Tsien F; Schwartz S
    Am J Hum Genet; 1994 May; 54(5):748-56. PubMed ID: 8178816
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Triplication of 15q11-q13 with inv dup(15) in a female with developmental delay.
    Long FL; Duckett DP; Billam LJ; Williams DK; Crolla JA
    J Med Genet; 1998 May; 35(5):425-8. PubMed ID: 9610809
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Inv dup del(10q): identification by fluorescence in situ hybridization and array comparative genomic hybridization in a fetus with two concurrent chromosomal rearrangements.
    Chen CP; Chen M; Su YN; Huang JP; Ma GC; Chang SP; Chern SR; Chen YT; Su JW; Lee CC; Town DD; Wang W
    Taiwan J Obstet Gynecol; 2012 Jun; 51(2):245-52. PubMed ID: 22795102
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cytogenetic and molecular characterization of inverted duplicated chromosomes 15 from 11 patients.
    Cheng SD; Spinner NB; Zackai EH; Knoll JH
    Am J Hum Genet; 1994 Oct; 55(4):753-9. PubMed ID: 7942854
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Cytogenetic and molecular analysis of inv dup(15) chromosomes observed in two patients with autistic disorder and mental retardation.
    Flejter WL; Bennett-Baker PE; Ghaziuddin M; McDonald M; Sheldon S; Gorski JL
    Am J Med Genet; 1996 Jan; 61(2):182-7. PubMed ID: 8669450
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Maternal uniparental disomy in a patient with Prader-Willi syndrome with an additional small inv dup(15) chromosome.
    Wang YM; Chuang L; Wang BT; Kuo PL
    J Formos Med Assoc; 2004 Dec; 103(12):943-7. PubMed ID: 15624046
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Inv dup del(9p): prenatal diagnosis and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization.
    Chen CP; Su YN; Chern SR; Hsu CY; Tsai FJ; Wu PC; Lee CC; Chen YT; Lee MS; Wang W
    Taiwan J Obstet Gynecol; 2011 Mar; 50(1):67-73. PubMed ID: 21482378
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cytogenetic characterization of an extra structurally abnormal chromosome associated with severe mental retardation: inv dup (15) (q13).
    Gorla N; Slavutsky I; Lisanti J; Pedrazzini E; Vanella L; Larripa I
    Hereditas; 1998; 129(1):1-5. PubMed ID: 9868924
    [TBL] [Abstract][Full Text] [Related]  

  • 18. FISH characterisation of dynamic mosaicism involving an inv dup(15) in a patient with mental retardation.
    Cockwell AE; Dávalos IP; Rivera HR; Crolla JA
    Am J Med Genet; 2001 Nov; 103(4):289-94. PubMed ID: 11746008
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A Down syndrome case with a karyotype of 46,XY,rec(21)dup(21q)inv(21)(p11q22) derived from paternal pericentric inversion of chromosome 21.
    Ilgin Ruhi H; Tükün A; Karabulut H; Bayazit P; Bökesoy I
    Clin Genet; 2001 May; 59(5):368-70. PubMed ID: 11359472
    [No Abstract]   [Full Text] [Related]  

  • 20. Clinical and molecular analysis of five inv dup(15) patients.
    Robinson WP; Binkert F; Giné R; Vazquez C; Müller W; Rosenkranz W; Schinzel A
    Eur J Hum Genet; 1993; 1(1):37-50. PubMed ID: 8069650
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.