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 *

567 related articles for article (PubMed ID: 9599644)

  • 21. Pallister-Killian Syndrome (PKS) as a Cause of Mental Retardation.
    Shamdeen A; Meyer S; Gottschling S; Oehl-Jaschkowitz B; Gortner L; Shamdeen MG
    Klin Padiatr; 2009; 221(2):97-9. PubMed ID: 19067289
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Partial trisomy 15 in a male with severe psychomotor retardation (48, XY, + 15q -, + mar(15)).
    Voss R; Lerer I; Maftzir G; Sheinis M; Cohen MM
    Am J Med Genet; 1982 Jun; 12(2):131-9. PubMed ID: 7102721
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Cytogenetic abnormalities in orthopedic patients.
    Cowell HR; Clark CE
    Clin Orthop Relat Res; 1978 Sep; (135):4-14. PubMed ID: 152176
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Unbalanced inherited complex chromosome rearrangement involving chromosome 8, 10, 11 and 16 in a patient with congenital malformations and delayed development.
    Karmous-Benailly H; Giuliano F; Massol C; Bloch C; De Ricaud D; Lambert JC; Perelman S
    Eur J Med Genet; 2006; 49(5):431-8. PubMed ID: 16497571
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Molecular and cytogenetic characterisation of an unusual case of partial trisomy/partial monosomy 13 mosaicism: 46,XX,r(13)(p11q14)/46,XX,der(13)t(13;13)(q10;q14).
    Gentile M; Buonadonna AL; Cariola F; Fiorente P; Valenzano MC; Guanti G
    J Med Genet; 1999 Jan; 36(1):77-82. PubMed ID: 9950374
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Subtelomeric chromosomal rearrangements detected in patients with idiopathic mental retardation and dysmorphic features.
    Caliskan MO; Karauzum SB; Mihci E; Tacoy S; Luleci G
    Genet Couns; 2005; 16(2):129-38. PubMed ID: 16080292
    [TBL] [Abstract][Full Text] [Related]  

  • 27. De novo highly complex chromosome rearrangement (CCR) involving five breakpoints with congenital anomalies analyzed by FISH.
    Curotti G; Benkhalifa M; Raybaud C; Picard F; Bellec V; Qumsiyeh MB
    Genet Couns; 1999; 10(3):259-64. PubMed ID: 10546097
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Trisomy of the distal 15q region due to familial balanced translocation t(15;16)(q24;p13) and unusual mosaicism in the mother of the proband].
    Nazarenko SA; Nazarenko LP; Baranova VA
    Tsitol Genet; 1987; 21(6):434-7. PubMed ID: 3445362
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Chromosome missegregation and trisomy 21 mosaicism in Alzheimer's disease.
    Geller LN; Potter H
    Neurobiol Dis; 1999 Jun; 6(3):167-79. PubMed ID: 10408806
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Prenatal diagnosis of de novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements.
    Chen CP; Chern SR; Lee CC; Lin CC; Li YC; Hsieh LJ; Chen WL; Wang W
    Prenat Diagn; 2006 Feb; 26(2):138-46. PubMed ID: 16470734
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A complex chromosome rearrangement with at least five breakpoints studied by fluorescence in situ hybridization.
    Gibson LH; McGrath J; Yang-Feng TL
    Am J Med Genet; 1997 Feb; 68(4):417-20. PubMed ID: 9021014
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [An analysis of human marker chromosomes originating from chromosome 21 by using in situ hybridization].
    Zerova TE; Baronova EV; Gorovenko NG; Koblianskaia GN; Buzhievskaia TI; Vorsanova SG; Iurov IuB
    Tsitol Genet; 1995; 29(5):41-8. PubMed ID: 8721845
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Detection of an unbalanced t(4;15) by FISH in a child with multiple congenital anomalies.
    Celep F; Acar H; Aynaci O; Aynaci FM; Karagüzel A
    Genet Couns; 2001; 12(4):319-26. PubMed ID: 11837600
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Inv dup(15) supernumerary marker chromosomes.
    Webb T
    J Med Genet; 1994 Aug; 31(8):585-94. PubMed ID: 7815414
    [No Abstract]   [Full Text] [Related]  

  • 35. A case of mosaic Down's syndrome with two Robertsonian translocations.
    Leal-Garza CH; Cortés-Gutiérrez EI; Ortiz-Jalomo R; García-Cavazos R
    Rev Invest Clin; 1996; 48(5):385-8. PubMed ID: 8968157
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Cytogenetic characterization of cat eye syndrome marker chromosome.
    Wenger SL; Surti U; Nwokoro NA; Steele MW
    Ann Genet; 1994; 37(1):33-6. PubMed ID: 8010712
    [TBL] [Abstract][Full Text] [Related]  

  • 37. An approach for quantitative assessment of fluorescence in situ hybridization (FISH) signals for applied human molecular cytogenetics.
    Iourov IY; Soloviev IV; Vorsanova SG; Monakhov VV; Yurov YB
    J Histochem Cytochem; 2005 Mar; 53(3):401-8. PubMed ID: 15750029
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 18q- and 18q+ mosaicism in a mentally retarded boy.
    Ausems MG; Bhola SL; Post-Blok CA; Hennekam RC; de France HF
    Am J Med Genet; 1994 Nov; 53(3):296-9. PubMed ID: 7856666
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Delineation of a supernumerary marker chromosome utilizing a multimodal approach of G-banding, fluorescent in situ hybridization, confirmatory P1 artificial chromosome fluorescent in situ hybridization, and high-resolution comparative genomic hybridization.
    Mark HF; Wyandt H; Huang XL; Milunsky JM
    Clin Genet; 2005 Aug; 68(2):146-51. PubMed ID: 15996211
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Mosaicism for del(17)(p11.2p11.2) underlying the Smith-Magenis syndrome.
    Juyal RC; Kuwano A; Kondo I; Zara F; Baldini A; Patel PI
    Am J Med Genet; 1996 Dec; 66(2):193-6. PubMed ID: 8958329
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 29.