BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

487 related articles for article (PubMed ID: 5565831)

  • 21. Partial trisomy 12p. A newborn child with karyotype 46,XY,der(11), t(11; 12) (q25; p11) mat. Case report and review.
    Ottolina de Bracamonte N; Velazco JQ; Hammond Figueroa FG
    Acta Cient Venez; 1982; 33(4):342-7. PubMed ID: 7186725
    [No Abstract]   [Full Text] [Related]  

  • 22. [A case of C-D translocation in a 9 year old boy and his mother].
    Revazov AA; Russkikh VV
    Tsitologiia; 1966; 8(2):269-76. PubMed ID: 5984073
    [No Abstract]   [Full Text] [Related]  

  • 23. A ring chromosome (46,XY,13r) occurring in a family with a D-D translocation 13-,14-, t(13q 14q).
    Mikkelsen M; Niebuhr E
    Ann Genet; 1969 Mar; 12(1):51-6. PubMed ID: 5306712
    [No Abstract]   [Full Text] [Related]  

  • 24. [Familial translocation t(4;22) (p11;p12) and trisomy 4p in 2 sisters].
    Giovannelli G; Forabosco A; Dutrillaux B
    Ann Genet; 1974 Jun; 17(2):119-24. PubMed ID: 4547939
    [No Abstract]   [Full Text] [Related]  

  • 25. [Partial C trisomy through translocation t(Cp-;Gp-)].
    Deminatti M; Maillard E; Gosselin B; Peltier JM; Bulteel MF; Dupuis C
    Ann Genet; 1969 Mar; 12(1):36-45. PubMed ID: 5306710
    [No Abstract]   [Full Text] [Related]  

  • 26. Familial transmission of a Gq- (Ph1-like) chromosome.
    Ricci N; Dallapiccola B; Preto G
    Ann Genet; 1970 Dec; 13(4):263-4. PubMed ID: 5313390
    [No Abstract]   [Full Text] [Related]  

  • 27. [Karyological study of human spontaneous and medical abortions].
    Golovachev GD; Slozina NM; Petrova SP
    Tsitologiia; 1973 Jul; 15(7):948-52. PubMed ID: 4779389
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Proximal 14 trisomy 46,XX, -22 +der(14)t(14;22) (q21;q11)mat.
    Fried K; Goldberg MD; Rosenblatt M
    Teratology; 1980 Jun; 21(3):309-12. PubMed ID: 7455919
    [No Abstract]   [Full Text] [Related]  

  • 29. Partial monosomy of a G group chromosome (45,XY,G-46,XY,Gr): report of a new case.
    Armendares S; Buentello L; Cantu-Garza JM
    Ann Genet; 1971 Mar; 14(1):7-12. PubMed ID: 5314299
    [No Abstract]   [Full Text] [Related]  

  • 30. [Partial monosomy of a C group chromosome (Cp-)].
    Laurent C; Nivelon A; Hartman E; Guerrier G
    Ann Genet; 1968 Dec; 11(4):231-5. PubMed ID: 5306365
    [No Abstract]   [Full Text] [Related]  

  • 31. [Clinical and cytogenetic observations on 2 mosaic C trisomic adults. Individualization of the supernumerary chromosome with the modern denaturation technic: 47, XY, ?8 +].
    Laurent C; Robert JM; Grambert J; Dutrillaux B
    Lyon Med; 1971 Dec; 226(20):827-33. PubMed ID: 5144392
    [No Abstract]   [Full Text] [Related]  

  • 32. [Translocation 46,XX, t(15; 21) (q13; q22,1) in the mother of 2 children with partial trisomy 15 and monosomy 21].
    Rethoré MO; Dutrillaux B
    Ann Genet; 1973 Dec; 16(4):271-5. PubMed ID: 4544092
    [No Abstract]   [Full Text] [Related]  

  • 33. Elucidation of the cytogenetic abnormality in a 4p- "phenocopy".
    Curry CJ; Ying KL; O'Lague P; Tsai J
    Birth Defects Orig Artic Ser; 1982; 18(3B):275-86. PubMed ID: 7139110
    [No Abstract]   [Full Text] [Related]  

  • 34. Meiotic segregation in familial reciprocal translocation t(8q;22q).
    Gödde-Salz E; Oesinghaus S; Grote W
    Am J Med Genet; 1982 Feb; 11(2):241-7. PubMed ID: 7065009
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Mental retardation, malformation syndrome andpartial 7p monosomy [45, XX, tdic (7;15) (p21;p11)].
    Nakagome Y; Teramura F; Katoaka K; Hosono F
    Clin Genet; 1976 Jun; 9(6):621-4. PubMed ID: 1277574
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Long arm deletion of chromosome no. 6 in a mentally retarded boy with multiple physical malformations.
    Milosević J; Kalicanin P
    J Ment Defic Res; 1975 Jun; 19(2):139-44. PubMed ID: 1195357
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Ring chromosome 22. Description of a new case (1)].
    Gil Benso R; López Ginés C; Gregori Romero M; Galán Sánchez F; Pellín Pérez A
    An Esp Pediatr; 1991 Jul; 35(1):62-4. PubMed ID: 1772175
    [No Abstract]   [Full Text] [Related]  

  • 38. A family with a presumptive C-F translocation in five generations.
    Therkelsen AJ; Klinge T; Henningsen K; Mikkelsen M; Schmidt G
    Ann Genet; 1971 Mar; 14(1):13-21. PubMed ID: 5314290
    [No Abstract]   [Full Text] [Related]  

  • 39. [The "Copenhagen chromosome" (syndrome of the small metacentric extra-chromosome)].
    Haberlandt W
    Arztl Forsch; 1971 Jul; 25(7):218-23. PubMed ID: 5109598
    [No Abstract]   [Full Text] [Related]  

  • 40. Partial deletion of the long arm of chromosome E-18.
    Curran JP; al-Salihi FL; Allderdice PW
    Pediatrics; 1970 Nov; 46(5):721-9. PubMed ID: 5481073
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 25.