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 *

129 related articles for article (PubMed ID: 1421359)

  • 1. Molecular cytogenetic study of short arm aberrations in human D, G group chromosomes.
    Wang Y; Cheng Z; Gao C; Fu S; Wang S; Fu H; Ye L; Ma S
    Chin Med Sci J; 1992 Mar; 7(1):27-31. PubMed ID: 1421359
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Molecular cytogenetic study of short arm aberrations in human D and G group chromosomes].
    Wang Y
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1992 Oct; 14(5):339-45. PubMed ID: 1299537
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Satellited Y chromosomes: structure, origin, and clinical significance.
    Schmid M; Haaf T; Solleder E; Schempp W; Leipoldt M; Heilbronner H
    Hum Genet; 1984; 67(1):72-85. PubMed ID: 6745929
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Loss of the Y chromosomal PAR2-region in four familial cases of satellited Y chromosomes (Yqs).
    Kühl H; Röttger S; Heilbronner H; Enders H; Schempp W
    Chromosome Res; 2001; 9(3):215-22. PubMed ID: 11330396
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular cytogenetic characterization of three familial cases of satellited Y chromosomes.
    Wilkinson TA; Crolla JA
    Hum Genet; 1993 May; 91(4):389-91. PubMed ID: 8500794
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Molecular cytogenetic study of supernumerary marker chromosomes in an unselected group of children.
    Gravholt CH; Friedrich U
    Am J Med Genet; 1995 Mar; 56(1):106-11. PubMed ID: 7747772
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Molecular and clinical cytogenetic studies of a family with a 22p+ marker chromosome].
    Liu S; Gao C; Hu Y; Liu M; Cheng Z
    Yi Chuan Xue Bao; 1993; 20(1):7-11. PubMed ID: 8507506
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Molecular cytogenetic study on the case with 14p+ marker chromosome].
    Cheng ZY; Gao CS; Xin X; Fu SM; Zhong WL
    Yi Chuan Xue Bao; 1989; 16(4):331-4. PubMed ID: 2486254
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Loss of the Y chromosome PAR2 region and additional rearrangements in two familial cases of satellited Y chromosomes: cytogenetic and molecular analysis.
    Velissariou V; Sismani C; Christopoulou S; Kaminopetros P; Hatzaki A; Evangelidou P; Koumbaris G; Bartsocas CS; Stylianidou G; Skordis N; Diakoumakos A; Patsalis PC
    Eur J Med Genet; 2007; 50(4):291-300. PubMed ID: 17584536
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The usefulness of NOR and RFA banding in prenatal diagnosis: a case report.
    Sciorra LJ; Rajendra B; Cummings E; Ekblom L; Lee M
    Am J Med Genet; 1981; 10(2):147-9. PubMed ID: 7315871
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Analysis of a familial 15p + polymorphism: exclusion of Y/15 translocation.
    Werner W; Herrmann FH
    Clin Genet; 1984 Sep; 26(3):204-8. PubMed ID: 6478640
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Cytogenetic and molecular genetic study on a female with complex translocation of t(Y;15) and t(14;21)].
    Shi Y; Ma S; Wang Y; Gao C; Ye L; Cheng Z
    Yi Chuan Xue Bao; 1993; 20(6):488-92. PubMed ID: 8179934
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Value of silver staining technics for the study of acrocentric ring chromosomes and supernumerary microchromosomes].
    Teyssier M; Moreau N
    C R Seances Soc Biol Fil; 1984; 178(3):251-6. PubMed ID: 6208982
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Familial cases of marker chromosomes of groups 21-22 and 13-15 (Gpss and Dp+).
    Kyaosaar ME
    Sov Genet; 1973 Nov; 7(7):913-8. PubMed ID: 4777944
    [No Abstract]   [Full Text] [Related]  

  • 15. [Frequency of Ag-stained NOR and satellite associations in four 14/21 translocation carriers and in their normal relatives (author's transl)].
    Carnevale A; Blanco B; Dora Moya J
    Rev Invest Clin; 1981; 33(4):365-8. PubMed ID: 6173908
    [No Abstract]   [Full Text] [Related]  

  • 16. A case of nondisjunction of chromosome 21 (47,X,Yqs,+21) in an Indian family with Yqs.
    Reddy KS; Thomas IM; Narayanan HS
    Ann Genet; 1984; 27(3):194-6. PubMed ID: 6334487
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Satellite DNA sequences in the human acrocentric chromosomes: information from translocations and heteromorphisms.
    Gosden JR; Lawrie SS; Gosden CM
    Am J Hum Genet; 1981 Mar; 33(2):243-51. PubMed ID: 6163355
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Clinical case of tandem translocation between chromosomes 13 and 15].
    Badalian LO; Arkhipov BA; Malygina NA; Patrukhin AS; Lysov VL
    Tsitol Genet; 1985; 19(4):304-8. PubMed ID: 4049521
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Silver staining of the supernumerary chromosome in the cat-eye syndrome.
    Petit P; Godart S; Fryns JP
    Ann Genet; 1980; 23(2):114-6. PubMed ID: 6156636
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Remarks on a satellited Y chromosome (author's transl)].
    Genest P
    Sem Hop; 1979 Apr 18-25; 55(15-16):799-800. PubMed ID: 227075
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.