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 *

130 related articles for article (PubMed ID: 548877)

  • 1. [Trisomy 13 q31 to qter due to duplication on the short arm of chromosome 7].
    Giuffrè L; Rindone E; Cammarata M; Lo Giudice C; Dallapiccola B
    Pathologica; 1979; 71(1013):356-8. PubMed ID: 548877
    [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. Trisomy 15q23----qter due to a de novo t(11;15)(q25;q23) and assignment of the critical segment.
    García-Cruz D; García-Esquivel L; Rivera H; Vaca G; Rolón A; Cantú JM
    Ann Genet; 1985; 28(3):193-6. PubMed ID: 3879157
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Autosomal chromosome aberrations in ophthalmology.
    Francois J
    Int Ophthalmol Clin; 1968; 8(4):839-910. PubMed ID: 4244691
    [No Abstract]   [Full Text] [Related]  

  • 5. [Observation of 7 cases of rare autosomal pathology. Trisomy 9p; monosomy 18q; ring 21; trisomy 6p; trisomy 2q 1-21 translocation].
    Fioretti G; Pagano L; Renda S; Festa B; Rinaldi A; Celona A; Casullo C; Stabile M; Cavaliere ML; Ventruto V
    Minerva Pediatr; 1980 Jun; 32(12):807-14. PubMed ID: 7464734
    [No Abstract]   [Full Text] [Related]  

  • 6. [2 cases of trisomy 11q(q231--qter) by translocation t(11;22) (q231;q111) in 2 different families].
    Aurias A; Turc C; Michiels Y; Sinet PM; Graveleau D; Lejeune J
    Ann Genet; 1975 Sep; 18(3):185-8. PubMed ID: 1080981
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Partial free trisomies and their formation through reciprocal translocations (author's transl)].
    Schwanitz G; Grosse KP
    Folia Clin Int (Barc); 1973 Oct; 23(10):666-73. PubMed ID: 4805342
    [No Abstract]   [Full Text] [Related]  

  • 8. [2 cases of trisomy 11q(q23.2-- qter) with the same abnormality of external genitalia].
    Laurent C; Biemont MC; Bethenod M; Cret L; David M
    Ann Genet; 1975 Sep; 18(3):179-84. PubMed ID: 1080980
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A de novo tandem duplication 15(q21 leads to qter) mosaic.
    Yip MY; Parsons A; Hultén M
    Clin Genet; 1982 Jul; 22(1):1-6. PubMed ID: 7172470
    [No Abstract]   [Full Text] [Related]  

  • 10. [Trisomy 10p as a result of familial 10/22 translocation].
    Zergollern L; Begovic D; Muzinić D
    Acta Med Iugosl; 1980; 34(2):113-22. PubMed ID: 7405617
    [No Abstract]   [Full Text] [Related]  

  • 11. Developmental and other pathologic changes in syndromes caused by chromosome abnormalities.
    Gilbert EF; Opitz JM
    Perspect Pediatr Pathol; 1982; 7():1-63. PubMed ID: 6214761
    [No Abstract]   [Full Text] [Related]  

  • 12. De novo tandem duplication of the middle segment of the long arm of chromosome 14.
    Ito M; Mutoh K; Okuno T; Mikawa H; Edagawa J; Abe T
    Ann Genet; 1983; 26(2):116-9. PubMed ID: 6604486
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [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]  

  • 14. Partial trisomy 13 in an infant with a mild phenotype: application of fluorescence in situ hybridization in cytogenetic syndromes.
    Begovic D; Hitrec V; Lasan R; Letica L; Baric I; Sarnavka V; Galic S
    Croat Med J; 1998 Jun; 39(2):212-5. PubMed ID: 9575279
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [The intelligence level in the chromosome aberrations affecting autosomes].
    Moor L
    Rev Neuropsychiatr Infant; 1970 Dec; 18(12):943-66. PubMed ID: 4251821
    [No Abstract]   [Full Text] [Related]  

  • 16. Distal trisomy 14q due to tandem duplication (q24 leads to q32).
    Orye E; Van Bever H; Desimpel H
    Ann Genet; 1983; 26(4):238-9. PubMed ID: 6607705
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Trisomy of the short arm of chromosome number 9: a clinical entity.
    Fryns JP; van den Berghe H
    Acta Paediatr Belg; 1980; Suppl 13():97-104. PubMed ID: 7415833
    [No Abstract]   [Full Text] [Related]  

  • 18. [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]  

  • 19. [Partial trisomy 14q II.--Partial trisomy 14q due to a maternal t(12; 14) (q24.4; q21)].
    Turleau C; Grouchy J; Bocquentin F; Roubin M; Colin FC
    Ann Genet; 1975 Mar; 18(1):41-4. PubMed ID: 1080037
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Prenatal diagnosis of a de novo trisomy case 9q-47,XX,+9 del(q33----qter)].
    Cordier MP; Coicaud C; Thoulon JM; Robert JM; Germain D
    J Genet Hum; 1984 Dec; 32(5):351-61. PubMed ID: 6527131
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.