BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

472 related articles for article (PubMed ID: 5306710)

  • 1. [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]  

  • 2. Transmission of a translocation t(Cp+; Dq-) through three generations; including an example of probable trisomy for the short arm of the C group chromosome No. 9.
    Butler LJ; Eades SM; France NE
    Ann Genet; 1969 Mar; 12(1):15-27. PubMed ID: 5306708
    [No Abstract]   [Full Text] [Related]  

  • 3. [Partial trisomy C through a familial translocation t(Cq+;Cq-)].
    Lejeune J; Rethoré MO; Berger R; Abonyi D; Dutrillaux B; See G
    Ann Genet; 1968 Sep; 11(3):171-5. PubMed ID: 5304617
    [No Abstract]   [Full Text] [Related]  

  • 4. [Partial trisomy for the long arm of a C chromosome (?6) through t(Gp+;Cqs+) translocation].
    de Grouchy J; Emerit I; Aicardi J
    Ann Genet; 1969 Jun; 12(2):133-7. PubMed ID: 5308386
    [No Abstract]   [Full Text] [Related]  

  • 5. Partial trisomy 9 in the case of familial translocation 8/9 mat.
    Schwanitz G; Schamberger U; Rott HD; Wieczorek V
    Ann Genet; 1974 Sep; 17(3):163-6. PubMed ID: 4548816
    [No Abstract]   [Full Text] [Related]  

  • 6. [Partial trisomy 11q;22q (author's transl)].
    Benítez J; Ayuso C; García Aparicio J; Sáez E; Pérez Sotelo A; Bello MJ
    An Esp Pediatr; 1981 Sep; 15(3):293-300. PubMed ID: 7332142
    [No Abstract]   [Full Text] [Related]  

  • 7. Trisomy 6q22 leads to 6qter due to maternal 6;21 translocation. Case report review of the literature.
    Taysi K; Chao WT; Monaghan N; Monaco MP
    Ann Genet; 1983; 26(4):243-6. PubMed ID: 6364954
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Trisomy 9p gy t(4; 9) (q 34; q21) mat].
    Rethoré MO; Ferrand J; Dutrillaux B; Lejeune J
    Ann Genet; 1974 Sep; 17(3):157-61. PubMed ID: 4548815
    [No Abstract]   [Full Text] [Related]  

  • 9. Autosomal syndromes.
    Summitt RL
    Pediatr Ann; 1978 Jun; 7(6):94-5, 97-100, 102-7 passim. PubMed ID: 149945
    [No Abstract]   [Full Text] [Related]  

  • 10. [Autosomal chromosome aberrations].
    Serville F; Battin J
    Bord Med; 1971 May; 4(5):1373-416. PubMed ID: 5105683
    [No Abstract]   [Full Text] [Related]  

  • 11. [Partial 10q trisomy (q24;q ter) caused by a balanced maternal translocation t(6;10)(q26;q24)].
    Aledo AG; Gracia R; López Pajares I; González M; Oliver A; Peralta A
    An Esp Pediatr; 1982 Aug; 17(2):125-9. PubMed ID: 7149479
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Familial translocation between chromosomes of groups C and D (46, T(Cq-;Dq+).
    Tal'vik TA; Mikel'saar AV; Mikel'saar RV
    Sov Genet; 1974 Jun; 8(5):651-7. PubMed ID: 4413436
    [No Abstract]   [Full Text] [Related]  

  • 13. [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]  

  • 14. [Autosomal chromosome aberrations].
    Schinzel A
    Arch Genet (Zur); 1979; 52(1-2):1-204. PubMed ID: 389192
    [No Abstract]   [Full Text] [Related]  

  • 15. Relationship between anomalies of phenotype and karyotype in human embryogenesis.
    Kuliev AM
    Sov Genet; 1974 Jul; 8(7):910-20. PubMed ID: 4424716
    [No Abstract]   [Full Text] [Related]  

  • 16. [On three cases of C trisomy].
    Lejeune J; Dutrillaux B; Rethoré MO; Berger R; Debray H; Veron P; Gorce F; Grossiord A
    Ann Genet; 1969 Mar; 12(1):28-35. PubMed ID: 5306709
    [No Abstract]   [Full Text] [Related]  

  • 17. [Trisomy of the short arm of 9 with isochromosome 9p and partial monosomy Yq].
    Geneix A; Jaffray JY; Charbonne F; Perissel B; Malpuech G; Malet P; Roland MO
    Ann Genet; 1983; 26(2):103-5. PubMed ID: 6604482
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Cp trisomy: a new syndrome].
    Canu JM; Buentello L; Armendares S
    Ann Genet; 1971 Sep; 14(3):177-86. PubMed ID: 5315464
    [No Abstract]   [Full Text] [Related]  

  • 19. Translocation of 9q/13q resulting in duplication (trisomy 9pter leads to 9q22) and deficiency (monosomy 13pter leads to 13q12).
    Howard-Peebles PN; Yarbrough KM; Stoddard GR; Rary JM
    Clin Genet; 1977 Jan; 11(1):46-52. PubMed ID: 830449
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [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]  

    [Next]    [New Search]
    of 24.