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 *

93 related articles for article (PubMed ID: 302684)

  • 1. Mosaic 45,xy,-21/46,xy in a child with G deletion syndrome I.
    Olinici CD; Butnariu J; Popescu A; Giurguiman M
    Ann Genet; 1977 Jun; 20(2):115-7. PubMed ID: 302684
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Syndrome of multiple abnormalities in a child with mosaicism 46, XY/47, XY, +E].
    Balcar-Boroń A; Sawa H; Slowik J; Marcinkowska A; Robińska E
    Pediatr Pol; 1977 Oct; 52(10):1161-4. PubMed ID: 583678
    [No Abstract]   [Full Text] [Related]  

  • 3. [Clinical and cytogenetic considerations on a case of monosomy 21 in (45, XX-21/46,XY) mosaicism].
    Butnariu J; Olinici CD; Popescu A; Giurgiuman M
    Rev Pediatr Obstet Ginecol Pediatr; 1977; 26(4):331-6. PubMed ID: 414334
    [No Abstract]   [Full Text] [Related]  

  • 4. A case of ring (9)/del(9p) mosaicism associated with gastroesophageal reflux.
    Leung AK; Rudd NL
    Am J Med Genet; 1988 Jan; 29(1):43-8. PubMed ID: 3344775
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Ring chromosome 13 and multiple malformations (author's transl)].
    Antich J; Plaza J; Geán E
    An Esp Pediatr; 1981 Nov; 15(5):469-73. PubMed ID: 7332149
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. A case of interstitial 1q deletion [46,XY,del(q25q32.1)].
    Hamano S; Fukushima Y; Yamada T; Shimizu H; Okuyama M; Ito F; Maekawa K
    Ann Genet; 1987; 30(2):105-8. PubMed ID: 3314663
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Autosomal/heterosomal mixoploids: a report on two patients, a female with a 45, Z/47,XX plus 21 and a male with A 45,X/47,XY, plus 21 chromosome constitution.
    Hustinx TW; Haar BG; Scheres JM; Rutten FJ
    Ann Genet; 1974 Dec; 17(4):225-34. PubMed ID: 4281287
    [No Abstract]   [Full Text] [Related]  

  • 10. [Ring chromosomes in mosaicism 46, XY, Cr-46, XY].
    Ferrier S; Freund M; Grétillat A
    Arch Genet (Zur); 1973; 46(1):1-14. PubMed ID: 4731928
    [No Abstract]   [Full Text] [Related]  

  • 11. Identification by fluorescence of two G rings: (46,XY,21r) G deletion syndrome I and (46, XX, 22r) G deletion syndrome II.
    Magenis RE; Armendares S; Hecht F; Weleber RG; Overton K
    Ann Genet; 1972 Dec; 15(4):265. PubMed ID: 4539485
    [No Abstract]   [Full Text] [Related]  

  • 12. Novel isodicentric chromosome 18 in an abnormal infant with a mosaic karyotype [46,XY/46,XY,-18,+dic(18)(q12.2]).
    Bryke CR; Lindgren V; Fryburg JS; Yang-Feng TL
    Am J Med Genet; 1990 Jun; 36(2):247-50. PubMed ID: 2368814
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Wolf-Hirschhorn syndrome owing to 1:3 segregation of a maternal 4;21 translocation.
    Bauer K; Howard-Peebles PN; Keele D; Friedman JM
    Am J Med Genet; 1985 Jun; 21(2):351-6. PubMed ID: 4014316
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 46,XY-47,XY,C+ mosaicism in a male infant with multiple anomalies.
    Oikawa K; Kajii T; Shimba H; Sasaki M
    Ann Genet; 1969 Jun; 12(2):102-6. PubMed ID: 5308379
    [No Abstract]   [Full Text] [Related]  

  • 16. De novo satellited 21q associated with corpus callosum dysgenesis, colpocephaly, a concealed penis, congenital heart defects, and developmental delay.
    Chen CP; Lin SP; Chern SR; Lee CC; Huang JK; Wang W; Liao YW
    Genet Couns; 2004; 15(4):437-42. PubMed ID: 15658619
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinical findings in an Arab boy with ring (14)(mos 46,XY,r(14)/45,XY,-14).
    Portoian-Shuhaiber S; Al-Awadi S; Farag TI; Sundareshan TS; Jindal HR; Al-Rashied AA
    Ann Genet; 1986; 29(2):122-4. PubMed ID: 3490208
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Apparent Fryns syndrome in a boy with a tandem duplication of 1q24-31.2.
    Clark RD; Fenner-Gonzales M
    Am J Med Genet; 1989 Nov; 34(3):422-6. PubMed ID: 2596530
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Y chromosome structural abnormalities and Turner's syndrome].
    Ravel C; Siffroi JP
    Gynecol Obstet Fertil; 2009 Jun; 37(6):511-8. PubMed ID: 19464936
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [C-G translocation: karyotype 46, XY,t(Cq-; Gq+): parents 46, XX and 46, XY].
    Lambotte C; Carlier G; Frederic J; Keutgen J
    Acta Paediatr Belg; 1971; 25(2):119-26. PubMed ID: 5565831
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 5.