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 *

162 related articles for article (PubMed ID: 10756338)

  • 1. Three-year-old girl with partial trisomy 4p and partial monosomy 8p with resemblance to Brachmann-de Lange syndrome--another locus for Brachmann-de Lange syndrome on 4p?
    Mau UA; Backsch C; Schaudt H; Trefz FK; Kaiser P
    Am J Med Genet; 2000 Mar; 91(3):180-4. PubMed ID: 10756338
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Partial trisomy 4p and Brachmann-de Lange syndrome.
    Fryns JP
    Am J Med Genet; 2000 Dec; 95(4):406. PubMed ID: 11186901
    [No Abstract]   [Full Text] [Related]  

  • 3. Trisomy 12p and monosomy 4p: phenotype-genotype correlation.
    Benussi DG; Costa P; Zollino M; Murdolo M; Petix V; Carrozzi M; Pecile V
    Genet Test Mol Biomarkers; 2009 Apr; 13(2):199-204. PubMed ID: 19378504
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Trisomy 3q25.1-qter and monosomy 8p23.1-pter in a patient: cytogenetic and molecular analysis with delineation of the phenotype.
    Zafra de la Rosa G; Venegas-Vega CA; Monroy N; Contreras-Bucio G; Friedrich U; Houman M; Saad A; Fernández P; Kofman-Alfaro S; Cervantes A
    Am J Med Genet A; 2005 Jul; 136(3):259-64. PubMed ID: 15957183
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Dup(4p)del(9p) in a familial mental retardation syndrome. Resemblance to de Lange syndrome detected by high-resolution banding.
    Hersh JH; Dale KS; Gerald PS; Yen FF; Weisskopf B; Dinno ND
    Am J Dis Child; 1985 Jan; 139(1):81-4. PubMed ID: 3969990
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Partial monosomy 8p and partial trisomy 8p with moderate mental retardation.
    van Balkom ID; Hagendoorn J; De Pater JM; Hennekam RC
    Genet Couns; 1992; 3(2):83-9. PubMed ID: 1642815
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Partial duplication of 3q (q25.1-->q26.1) without the Brachmann-de Lange phenotype.
    Lopez-Rangel E; Dill FJ; Hrynchak MA; Van Allen MI
    Am J Med Genet; 1993 Nov; 47(7):1068-71. PubMed ID: 8291525
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular cytogenetic analysis of de novo partial monosomy 4p (4p16.2-->pter) and partial trisomy 8p (8p23.2-->pter).
    Chen CP; Lin SP; Chern SR; Lee CC; Chen LF; Chen YJ; Wang W
    Genet Couns; 2006; 17(1):81-5. PubMed ID: 16719283
    [No Abstract]   [Full Text] [Related]  

  • 9. Partial trisomy 3q causing mild Cornelia de Lange phenotype.
    Holder SE; Grimsley LM; Palmer RW; Butler LJ; Baraitser M
    J Med Genet; 1994 Feb; 31(2):150-2. PubMed ID: 8182724
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Classical West "syndrome" phenotype with a subtelomeric 4p trisomy.
    Gérard-Blanluet M; Romana S; Munier C; Le Lorc'h M; Kanafani S; Sinico M; Touboul C; Levaillant JM; Haddad B; Lopez N; Lelong F; De Villemeur TB; Verloes A; Borghi E
    Am J Med Genet A; 2004 Oct; 130A(3):299-302. PubMed ID: 15378535
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A severely mentally and motor retarded girl with monosomy 3pter-->p25 and trisomy 8q24-->qter due to a familial reciprocal translocation t(3;8)(p25;q24).
    Balci S; Aypar E; Beksaç MS; Bartsch O
    Genet Couns; 2009; 20(2):125-32. PubMed ID: 19650409
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prometaphase chromosomes in five patients with the Brachmann-de Lange syndrome.
    Breslau EJ; Disteche C; Hall JG; Thuline H; Cooper P
    Am J Med Genet; 1981; 10(2):179-86. PubMed ID: 7315874
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clinical and molecular cytogenetic characterization of two patients with partial trisomy 1q41-qter: further delineation of partial trisomy 1q syndrome.
    Emberger W; Petek E; Kroisel PM; Zierler H; Wagner K
    Am J Med Genet; 2001 Dec; 104(4):312-8. PubMed ID: 11754067
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Duplication 4p and deletion 4p (Wolf-Hirschhorn syndrome) due to complementary gametes from a 3:1 segregation of a maternal balanced t(4;13)(p16;q11) translocation.
    Takeno SS; Corbani M; Andrade JA; Smith Mde A; Brunoni D; Melaragno MI
    Am J Med Genet A; 2004 Aug; 129A(2):180-3. PubMed ID: 15316961
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Familial subtelomeric abnormality der(4)t(4p16.3;21q22.3) as a cause of mental retardation and mild dysmorphic features].
    Obersztyn E; Klapecki J; Helias-Rodzewicz Z; Bocian E; Mazurczak T
    Med Wieku Rozwoj; 2006; 10(1 Pt 2):199-209. PubMed ID: 17028389
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Syndrome of microcephaly, Brachmann-de Lange-like facial changes, severe metatarsus adductus, and developmental delay: mild Brachmann-de Lange syndrome?
    Halal F; Silver K
    Am J Med Genet; 1992 Feb; 42(3):381-6. PubMed ID: 1536185
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Partial trisomy and monosomy 8p due to inversion duplication.
    Engelen JJ; de Die-Smulders CE; Fryns JP; Hoovers JM; Albrechts JC; Loots WJ; Jacobs ME; Hamers AJ
    Clin Genet; 1994 Apr; 45(4):203-7. PubMed ID: 8062440
    [TBL] [Abstract][Full Text] [Related]  

  • 18. De novo case of a partial trisomy 4p and a partial monosomy 8p.
    Skrlec I; Wagner J; Pubeljić S; Heffer M; Stipoljev F
    Coll Antropol; 2014 Mar; 38(1):319-23. PubMed ID: 24851635
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Chromosomes in the Cornelia de Lange syndrome.
    Beck B; Mikkelsen M
    Hum Genet; 1981; 59(4):271-6. PubMed ID: 7333580
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Two cases of partial trisomy 8p and partial monosomy 21q in a family with a reciprocal translocation (8;21)(p21.1;q22.3).
    Plomp AS; Engelen JJ; Albrechts JC; de Die-Smulders CE; Hamers AJ
    J Med Genet; 1998 Jul; 35(7):604-8. PubMed ID: 9678708
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.