These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

177 related articles for article (PubMed ID: 15633165)

  • 21. Partial trisomy of chromosome 6q: an interstitial duplication of the long arm.
    Zneimer SM; Ziel B; Bachman R
    Am J Med Genet; 1998 Nov; 80(2):133-5. PubMed ID: 9805129
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Supernumerary ring chromosome 8: clinical and molecular cytogenetic characterization in a case report.
    Demori E; Devescovi R; Benussi DG; Dolce S; Carrozzi M; Villa N; Miertus J; Amoroso A; Pecile V
    Am J Med Genet A; 2004 Oct; 130A(3):288-94. PubMed ID: 15378554
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Trisomy 17p10-p12 due to mosaic supernumerary marker chromosome: delineation of molecular breakpoints and clinical phenotype, and comparison to other proximal 17p segmental duplications.
    Yatsenko SA; Treadwell-Deering D; Krull K; Lewis RA; Glaze D; Stankiewicz P; Lupski JR; Potocki L
    Am J Med Genet A; 2005 Oct; 138A(2):175-80. PubMed ID: 16152635
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Partial duplication of the short arm of chromosome 2 (dup(2)(p13----p21) associated with mental retardation and an Aarskog-like phenotype.
    Fryns JP; Kleczkowska A; Kenis H; Decock P; Van den Berghe H
    Ann Genet; 1989; 32(3):174-6. PubMed ID: 2573314
    [TBL] [Abstract][Full Text] [Related]  

  • 25. De novo 1q32q44 duplication and distal 1q trisomy syndrome.
    Nowaczyk MJ; Bayani J; Freeman V; Watts J; Squire J; Xu J
    Am J Med Genet A; 2003 Jul; 120A(2):229-33. PubMed ID: 12833404
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Partial tetrasomy 15 due to a unique inverted triplication of chromosome15q24-q26.
    James PA; Aftimos S; Oei P
    Am J Med Genet A; 2004 Oct; 130A(2):208-10. PubMed ID: 15372521
    [No Abstract]   [Full Text] [Related]  

  • 27. First clinical case of small de novo duplication of 19q (13.3-13.4) confirmed by FISH.
    Bhat M; Morrison PJ; Getty A; McManus D; Tubman R; Nevin NC
    Am J Med Genet; 2000 Mar; 91(3):201-3. PubMed ID: 10756343
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Genotype/phenotype analysis in a patient with pure and complete trisomy 12p.
    Zumkeller W; Volleth M; Muschke P; Tönnies H; Heller A; Liehr T; Wieacker P; Stumm M
    Am J Med Genet A; 2004 Sep; 129A(3):261-4. PubMed ID: 15326625
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Duplication of distal 22q.
    Abeliovich D; Maor E; Bashan N; Carmi R
    Am J Med Genet; 1989 Mar; 32(3):346-9. PubMed ID: 2729354
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Partial trisomy for short arm of chromosome 5.
    Yasutomo K; Suzue T; Nishioka A; Kozan H; Sekiguchi T; Ohara K; Okamoto T; Iwai T; Endo S
    Acta Paediatr Jpn; 1993 Aug; 35(4):336-9. PubMed ID: 8379327
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Clinical and molecular cytogenetic studies in a case with partial trisomy 12p due to a de novo supernumerary ring chromosome.
    Ausems MG; Schuil J; Van Raveswaaij-Arts C; De Pater JM
    Genet Couns; 2004; 15(4):405-10. PubMed ID: 15658615
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Trisomy of the short arm of chromosome 5: autopsy data in a malformed newborn with inv dup (5) (p13.1----p15.3).
    Kleczkowska A; Fryns JP; Moerman P; Vandenberghe K; Van den Berghe H
    Clin Genet; 1987 Jul; 32(1):49-56. PubMed ID: 3621654
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Inverted duplication of chromosome 5p14p15.3 confirmed with in situ hybridization.
    Zenger-Hain JL; Van Dyke DL; Wiktor A; Walker H; Feldman GL
    Am J Med Genet; 1993 Dec; 47(8):1198-201. PubMed ID: 8291556
    [TBL] [Abstract][Full Text] [Related]  

  • 34. FISH identifies different types of duplications with 12q13-15 as the commonly involved segment in B-cell lymphoproliferative malignancies characterized by partial trisomy 12.
    Dierlamm J; Wlodarska I; Michaux L; Vermeesch JR; Meeus P; Stul M; Criel A; Verhoef G; Thomas J; Delannoy A; Louwagie A; Cassiman JJ; Mecucci C; Hagemeijer A; Van den Berghe H
    Genes Chromosomes Cancer; 1997 Oct; 20(2):155-66. PubMed ID: 9331566
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Molecular cytogenetic analysis of a de novo interstitial chromosome 10q22 deletion.
    Tzschach A; Krause-Plonka I; Menzel C; Knoblauch A; Toennies H; Hoeltzenbein M; Radke M; Ropers HH; Kalscheuer V
    Am J Med Genet A; 2006 May; 140(10):1108-10. PubMed ID: 16619204
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Duplication 20p identified via fluorescent in situ hybridization.
    LeChien KA; McPherson E; Estop AM
    Am J Med Genet; 1994 Apr; 50(2):187-9. PubMed ID: 7516625
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Characterization of a familial balanced rec(13) in a child with mild MR and his half-sibling with two structurally rearranged chromosomes 13.
    Mehra S; Christ L; Jeng L; Zinn AB; Schwartz S
    Am J Med Genet A; 2005 Aug; 137(2):217-21. PubMed ID: 16059944
    [TBL] [Abstract][Full Text] [Related]  

  • 38. M-banding characterization of a 16p11.2p13.1 tandem duplication in a child with autism, neurodevelopmental delay and dysmorphism.
    Behjati F; Shafaghati Y; Firouzabadi SG; Kahrizi K; Bagherizadeh I; Najmabadi H; Bint S; Ogilvie C
    Eur J Med Genet; 2008; 51(6):608-14. PubMed ID: 18674645
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Trisomy 20q13 --> 20qter in a girl with multiple congenital malformations and a recombinant chromosome 20 inherited from a paternal inversion (20)(p13q13.1): clinical report and review of the trisomy 20q phenotype.
    Grange DK; Garcia-Heras J; Kilani RA; Lamp S
    Am J Med Genet A; 2005 Sep; 137A(3):308-12. PubMed ID: 16092120
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Cytogenetic and molecular identification of a de novo direct duplication of the long arm of chromosome 4(q21.3-->q31.3).
    Jeziorowska A; Ciesla W; Houck GE; Yao XL; Harris MS; Truszczak B; Skorski M; Jakubowski L; Jenkins EC; Kaluzewski B
    Am J Med Genet; 1993 Apr; 46(1):83-7. PubMed ID: 7684191
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.