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 *

161 related articles for article (PubMed ID: 739262)

  • 1. [Non-fluorescent Y chromosome in a 45,X/46,XY mosaic (author's transl)].
    Kaluzewski B; Jakubowski L; Moruzgala T; Bjanid O; Romer TE
    J Genet Hum; 1978 Sep; 26(3):255-35. PubMed ID: 739262
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Phenotype/karyotype correlations of Y chromosome aneuploidy with emphasis on structural aberrations in postnatally diagnosed cases.
    Hsu LY
    Am J Med Genet; 1994 Nov; 53(2):108-40. PubMed ID: 7856637
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Clinical consequences of a human non-fluorescent Y chromosome (Ynf).
    Sahdev S; Verma RS; Macera MJ; Vohra K; Jhaveri RC; Flores R
    Ann Genet; 1989; 32(4):241-3. PubMed ID: 2610491
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mixed gonadal dysgenesis with 45,X/46,X,idic(Y)/46,XY,idic(Y) karyotype.
    Caglayan AO; Demiryilmaz F; Kendirci M; Ozyazgan I; Akalin H; Bittmann S
    Genet Couns; 2009; 20(2):173-9. PubMed ID: 19650415
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A theory explaining the abnormality in 45,X/46,XY mosaicism with non-fluorescent Y chromosome. presentation of three cases.
    Kaluzewski B; Jokinen A; Hortling H; de la Chapelle A
    Ann Genet; 1978 Mar; 21(1):5-11. PubMed ID: 308343
    [TBL] [Abstract][Full Text] [Related]  

  • 6. XO/XY mosaicism with non fluorescent Y chromosome: clinical, cytogenetic and endocrinological studies on a female subject.
    Melis GB; Mameli M; Cardia S; Genazzani AR; Milia A; Nasi A; Paoletti AM; Puddu R; Fioretti P
    Acta Eur Fertil; 1977 Dec; 8(4):283-96. PubMed ID: 610313
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 45,X/46,X,dic(Yq) mosaicism and mixed gonadal dysgenesis. Case report and review of the literature.
    Armandares S; Salamanca F; Cos J; Chavarria C
    Ann Genet; 1977 Dec; 20(4):269-72. PubMed ID: 305755
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Bilateral gonadoblastoma in a phenotypic female with 45,X/46,X, dicentric iso Y [45,X/46,X,idic(Yq)] mosaicism.
    King CR; Cook DM
    Birth Defects Orig Artic Ser; 1978; 14(6C):109-22. PubMed ID: 569512
    [No Abstract]   [Full Text] [Related]  

  • 9. An infant with a mosaic 45,X/46,X,psu dic(Y) (pter-->q11.2::q11.2-->pter) karyotype and mixed gonadal dysgenesis studied for extent of mosaicism in the gonads.
    Reddy KS; Sulcova V; Ho CK; Conner ED; Khurana A
    Am J Med Genet; 1996 Dec; 66(4):441-4. PubMed ID: 8989464
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Identification of ring Y chromosome: cytogenetic analysis, Southern blot and fluorescent in situ hybridization.
    Pezzolo A; Perroni L; Gimelli G; Arslanian A; Porta S; Gandullia P; Gandullia E
    Ann Genet; 1993; 36(2):121-5. PubMed ID: 8215218
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A case with mosaic di-, tetra-, and octacentric ring Y chromosomes.
    Henegariu O; Pescovitz OH; Vance GH; Verbrugge J; Heerema NA
    Am J Med Genet; 1997 Sep; 71(4):426-9. PubMed ID: 9286449
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Dynamic mosaicism manifesting as loss, gain and rearrangement of an isodicentric Y chromosome in a male child with growth retardation and abnormal external genitalia.
    Iourov IY; Vorsanova SG; Liehr T; Monakhov VV; Soloviev IV; Yurov YB
    Cytogenet Genome Res; 2008; 121(3-4):302-6. PubMed ID: 18758177
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Rare structural rearrangement of the Y chromosome (Yq-,S) in the family of a boy with a sex differentiation disorder].
    Verlinskaia DK; Kovaleva NV; Prozorova MV; Khitrikova LE
    Tsitologiia; 1983 Feb; 25(2):204-6. PubMed ID: 6134363
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A variant Klinefelter syndrome patient with an XXY/XX/XY karyotype studied by GTG-banding and fluorescence in situ hybridization.
    Mark HF; Bai H; Sotomayor E; Mark S; Zolnierz K; Airall E; Sigman M
    Exp Mol Pathol; 1999 Sep; 67(1):50-6. PubMed ID: 10493892
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Dicentric Yp chromosome as one of the reasons for the absence of fluorescence in human Y chromosome].
    Verlinskaia DK; Prozorova MV
    Tsitologiia; 1983 Jun; 25(6):696-8. PubMed ID: 6684338
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [A new observation of an H-Y antigen positive 46, XX male (author's transl)].
    Heim J; Amice-Chambon V; Lemée F; Massart C
    Sem Hop; 1982 Jan; 58(2):79-83. PubMed ID: 6277000
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [A case of male pseudohermaphroditism with structural abnormalities of Y chromosome (ring Y)].
    Watanabe H; Hachisuka Y; Watase H; Fushimi N; Ohtaguro K
    Hinyokika Kiyo; 1988 Aug; 34(8):1469-74. PubMed ID: 3057830
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Identification of Y-chromosomal DNA in a Turner syndrome mosaic by polymerase chain reaction.
    Louie E; Nemeti M; Torfi H; Poskanzer LB; Anderson FR; Johnson JP
    Ann Genet; 1991; 34(3-4):252-5. PubMed ID: 1809235
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. [Further study on the nature of a multicentury small Y chromosome (author's transl)].
    Genest P
    Ann Genet; 1981; 24(3):165-6. PubMed ID: 6974527
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.