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 *

95 related articles for article (PubMed ID: 11840493)

  • 21. De novo t(5p;21q) in a patient previously diagnosed as monosomy 21.
    López-Pajares I; Martin-Ancel A; Cabello P; Delicado A; Garcia-Alix A; San Roman C
    Clin Genet; 1993 Feb; 43(2):94-7. PubMed ID: 8448910
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Familial arthrogryposis with distal involvement of the limbs.
    Kasai T; Oki T; Osuga T; Nogami H
    Clin Orthop Relat Res; 1982 Jun; (166):182-4. PubMed ID: 7083669
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Child with Sotos phenotype and a 5:15 translocation.
    Maroun C; Schmerler S; Hutcheon RG
    Am J Med Genet; 1994 Apr; 50(3):291-3. PubMed ID: 8042674
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Double chromosome anomaly: interstitial deletion 5q and reciprocal translocation (1;11)(p22;q21).
    de Michelena MI; Villacorta J; Chávez J
    Am J Med Genet; 1990 May; 36(1):29-32. PubMed ID: 2185634
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Bilateral microphthalmos with colobomatous orbital cyst and de-novo balanced translocation t(3;5).
    Kurbasic M; Jones FV; Cook LN
    Ophthalmic Genet; 2000 Dec; 21(4):239-42. PubMed ID: 11135495
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Cytogenetic and molecular study of a jumping translocation in a baby with Dandy-Walker malformation.
    Lefort G; Blanchet P; Chaze AM; Girardet A; Sarda P; Demaille J; Pellestor F
    J Med Genet; 2001 Jan; 38(1):67-73. PubMed ID: 11334011
    [No Abstract]   [Full Text] [Related]  

  • 27. A case of insertional translocation involving chromosomes 2 and 4.
    Asamoah A; Nandi KN; Prouty L; Thurmon TF; Chen H
    Clin Genet; 1998 Feb; 53(2):142-6. PubMed ID: 9611076
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Confirmation of a balanced chromosomal translocation using molecular techniques.
    Smart RD; Retief AE; Overhauser J
    Prenat Diagn; 1989 Jul; 9(7):505-13. PubMed ID: 2771889
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A de novo balanced t(2;6)(p15;p22.3) in a patient with West Syndrome disrupts a lnc-RNA.
    Vandeweyer G; Van der Aa N; Ceulemans B; van Bon BW; Rooms L; Kooy RF
    Epilepsy Res; 2012 May; 99(3):346-9. PubMed ID: 22245136
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Aminopterin-like syndrome sine aminopterin associated with translocation involving chromosomes 5 and 10.
    Chen MF; Vekemans M; Meagher-Villemure K; Outerbridge E; Fraser FC; Der Kaloustian VM
    Am J Med Genet; 1990 Dec; 37(4):478-81. PubMed ID: 2260592
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Coincidence of paternal 13pYq translocation and maternal increased 13p NOR activity in a child with arthrogryposis and other malformations.
    Bajnóczky K; Meggyessy V
    Acta Paediatr Hung; 1985; 26(2):151-6. PubMed ID: 4041282
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Cerebellar and brainstem hypoplasia in a child with a partial monosomy for the short arm of chromosome 5 and partial trisomy for the short arm of chromosome 10.
    Arts WF; Hofstee Y; Drejer GF; Beverstock GC; Oosterwijk JC
    Neuropediatrics; 1995 Feb; 26(1):41-4. PubMed ID: 7791950
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A de novo translocation of chromosomes 1 and 2 in an 18 year old boy with syndromic mental retardation.
    Neetha J; Girisha KM; Gopinath PM; Sekhar MR
    Genet Couns; 2012; 23(4):473-6. PubMed ID: 23431746
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Campomelic dysplasia associated with a de novo 2q;17q reciprocal translocation.
    Young ID; Zuccollo JM; Maltby EL; Broderick NJ
    J Med Genet; 1992 Apr; 29(4):251-2. PubMed ID: 1583645
    [TBL] [Abstract][Full Text] [Related]  

  • 35. De novo 1;10 balanced translocation in an infant with thanatophoric dysplasia: a clue to the locus of the candidate gene.
    Hersh JH; Yen FF; Peiper SC; Barch MJ; Yacoub OA; Voss DH; Roberts JL
    J Med Genet; 1995 Apr; 32(4):293-5. PubMed ID: 7643360
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Balanced translocation in a patient with severe myoclonic epilepsy of infancy disrupts the sodium channel gene SCN1A.
    Møller RS; Schneider LM; Hansen CP; Bugge M; Ullmann R; Tommerup N; Tümer Z
    Epilepsia; 2008 Jun; 49(6):1091-4. PubMed ID: 18294202
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Trisomy 2q and monosomy 11q in the same individual: the importance of considering the deleted segment.
    Ardinger HH; Patil SR; Rhead WJ
    Clin Genet; 1987 Jun; 31(6):381-5. PubMed ID: 3621640
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Prenatal diagnosis of a fetus with two balanced de novo chromosome rearrangements.
    Cotter PD; Caggana M; Willner JP; Babu A; Desnick RJ
    Am J Med Genet; 1996 Dec; 66(2):197-9. PubMed ID: 8958330
    [TBL] [Abstract][Full Text] [Related]  

  • 39. High-density array comparative genomic hybridization analysis and follow-up of a child with a de novo complex chromosome rearrangement detected prenatally.
    Quadrelli A; Vaglio A; Quadrelli R; Mechoso B; Fan YS; Huang T
    Prenat Diagn; 2007 Oct; 27(10):982-3. PubMed ID: 17899566
    [No Abstract]   [Full Text] [Related]  

  • 40. De novo concurrent 5p deletion and distal 17q duplication identified by fluorescence in situ hybridization (FISH).
    Szego K; Rauer M; Baratta E; Hoo JJ
    Ann Genet; 1993; 36(4):224-7. PubMed ID: 8166430
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.