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 *

138 related articles for article (PubMed ID: 5026850)

  • 21. Inherited t(13q14q) in two retarded sisters.
    Crandall BF; Francke U; Campbell MA; Sparkes RS
    Am J Hum Genet; 1972 Jul; 24(4):416-24. PubMed ID: 5031981
    [No Abstract]   [Full Text] [Related]  

  • 22. A 45,XX,21--child: attempt at a cytological and clinical interpretation of the karyotype.
    Gripenberg U; Elfving J; Gripenberg L
    J Med Genet; 1972 Mar; 9(1):110-5. PubMed ID: 5025474
    [No Abstract]   [Full Text] [Related]  

  • 23. New chromosomal malformation syndromes. I. Partial monosomy 8p. An attempt to establish a new chromosome deletion syndrome.
    Rodewald A; Stengel-Rutkowski S; Schulz P; Cleve H
    Eur J Pediatr; 1977 Apr; 125(1):45-57. PubMed ID: 870324
    [TBL] [Abstract][Full Text] [Related]  

  • 24. An 18p21q translocation in a patient with presumptive "monosomy G".
    Cohen MM; Putnam TI
    Am J Dis Child; 1972 Dec; 124(6):908-10. PubMed ID: 4639227
    [No Abstract]   [Full Text] [Related]  

  • 25. Trisomy of the short arm of chromosome 8: association with translocation between chromosomes 8 and 22 46,XY,22-,t(8p22q) plus.
    Rosenthal IM; Krmpotic E; Bocian M; Szego K
    Clin Genet; 1973 Jun; 4(6):507-16. PubMed ID: 4787842
    [No Abstract]   [Full Text] [Related]  

  • 26. Monosomy G: case report and review of the literature.
    Greenwood RD; Sommer A
    J Med Genet; 1971 Dec; 8(4):496-500. PubMed ID: 5149533
    [No Abstract]   [Full Text] [Related]  

  • 27. A child with a ring G chromosome (46,XX, Gr).
    Nevin NC; MacLaverty B; Campbell WA
    J Med Genet; 1971 Jun; 8(2):231-4. PubMed ID: 5096547
    [No Abstract]   [Full Text] [Related]  

  • 28. Study of a patient with apparent monosomy 21 owing to translocation: 45,XX,21-,t(18q+).
    Wyandt HE; Hecht F; Lovrien EW; Stewart RE
    Cytogenetics; 1971; 10(6):413-26. PubMed ID: 5146418
    [No Abstract]   [Full Text] [Related]  

  • 29. A ring chromosome, diagnosed by quinacrine fluorescence as No. 9, in a mentally retarded girl.
    Jacobsen P; Mikkelsen M; Rosleff F
    Clin Genet; 1973; 4(5):434-41. PubMed ID: 4127395
    [No Abstract]   [Full Text] [Related]  

  • 30. Deletion long arm 13.
    Nielsen J; Homma A; Christiansen F; Rasmussen K; Saldaña-Garcia P
    Hum Genet; 1977 Jul; 37(3):339-45. PubMed ID: 885554
    [No Abstract]   [Full Text] [Related]  

  • 31. "Antimongolism" syndrome.
    Endo A; Yamamoto M; Watanabe GI; Suzuki Y; Sakai K
    Br Med J; 1969 Oct; 4(5676):148-9. PubMed ID: 5823067
    [No Abstract]   [Full Text] [Related]  

  • 32. The 4p-syndrome, with a report of two new cases.
    Fryns JP; Eggermont E; Verresen H; Van den Berghe H
    Humangenetik; 1973; 19(1):99-109. PubMed ID: 4725911
    [No Abstract]   [Full Text] [Related]  

  • 33. A familial F/G translocation [t(p-; 22q+)] observed in three generations.
    Cohen MM; Davidson RG; Brown JA
    Clin Genet; 1975 Feb; 7(2):120-7. PubMed ID: 1132159
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Case report. Familial 4-22 translocation with partial trisomy for the short arm of chromosome 4 in two sibs.
    Sartori A; Tenconi R; Baccichetti C; Pujatti G
    Acta Paediatr Scand; 1974 Jul; 63(4):631-5. PubMed ID: 4850900
    [No Abstract]   [Full Text] [Related]  

  • 35. Ring chromosome 10:46,XX,r(10)(p15 leads to q26).
    Tsukino R; Tsuda N; Dezawa T; Ishii T; Koike M
    J Med Genet; 1980 Apr; 17(2):148-50. PubMed ID: 7381872
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Group G deletion syndromes.
    Kelch RP; Franklin M; Schmickel RD
    J Med Genet; 1971 Sep; 8(3):341-5. PubMed ID: 5097140
    [No Abstract]   [Full Text] [Related]  

  • 37. A patient with 45,XX,Gminus-46,XX,Gr mosaicism.
    Blank CE; Lorber J
    J Med Genet; 1969 Jun; 6(2):220-3. PubMed ID: 5801471
    [No Abstract]   [Full Text] [Related]  

  • 38. [Deletion of the short arm of chromosome 18 due to t(22-;18p+) translocation with IgA deficiency. Cytogenetic study with autoradiography and fluorescence].
    Gilgenkrantz S; Charles JM; Cabrol C; Mauuary G; Vigneron C
    Ann Genet; 1972 Dec; 15(4):275-81. PubMed ID: 4539488
    [No Abstract]   [Full Text] [Related]  

  • 39. 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]  

  • 40. Partial trisomy of 11 and 22 due to familial translocation t(11;22)(q23;q11), inherited in three generations.
    Nakai H; Yamamoto Y; Kuroki Y
    Hum Genet; 1979 Oct; 51(3):349-55. PubMed ID: 511169
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.