BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

87 related articles for article (PubMed ID: 890110)

  • 1. Trisomy 5: delineation of clinical features.
    DiLiberti JH; McKean R; Webb MJ; Williams G
    Birth Defects Orig Artic Ser; 1977; 13(3C):185-94. PubMed ID: 890110
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The trisomy 4p syndrome: case report and review.
    Gonzalez CH; Sommer A; Meisner LF; Elejalde BR; Opitz JM
    Am J Med Genet; 1977; 1(2):137-56. PubMed ID: 416713
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Case of partial trisomy 4p+ in a child as a result of a balanced translocation in the father].
    Patiutko RS; Kulieva LM; Egolina NA
    Genetika; 1978 Sep; 14(9):1653-7. PubMed ID: 720831
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Duplication (partial trisomy) of the distal long arm of chromosome 17: a new clinically recognizable chromosome disorder.
    Berberich MS; Carey JC; Lawce HJ; Hall BD
    Birth Defects Orig Artic Ser; 1978; 14(6C):287-95. PubMed ID: 728583
    [No Abstract]   [Full Text] [Related]  

  • 5. Trisomy 20p due to a paternal reciprocal translocation.
    Funderburk SJ; Sparkes RS; Sparkes MC
    Ann Genet; 1983; 26(2):94-7. PubMed ID: 6604493
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [De novo trisomy 4p by 4p isochromosome].
    André MJ; Aurias A; De Berranger P; Gillot F; Lefranc G; Lejeune J
    Ann Genet; 1976 Jun; 19(2):127. PubMed ID: 1085601
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Partial trisomy of chromosome 14: (+14q-).
    Yeatman GW; Riccardi VM
    Birth Defects Orig Artic Ser; 1976; 12(5):119-24. PubMed ID: 953211
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Partial trisomy 15q due to maternal translocation t(7;15)(q35;14)].
    Castel Y; Rivière D; Boycly JY; Toudic L
    Ann Genet; 1976 Mar; 19(1):15-9. PubMed ID: 1084116
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Short arm chromosome 4 trisomy. Clinical aspects of a new syndrome].
    Giovannelli G; Forabosco A; Rossi L; Solli R; Virdis R; Vanelli M; Pezzani C
    Minerva Pediatr; 1976 Mar; 28(7):401-4. PubMed ID: 1004436
    [No Abstract]   [Full Text] [Related]  

  • 10. Trisomy of the short arm of chromosome 4: the changing phenotype with age.
    Kleczkowska A; Fryns JP; van den Berghe H
    Ann Genet; 1992; 35(4):217-23. PubMed ID: 1296518
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Partial 14q trisomy. I. Partial 14q trisomy by maternal translocation t(10;14) (p15.2;q22)].
    Raoul O; Rethoré MO; Dutriliaux B; Michon L; Lejeune J
    Ann Genet; 1975 Mar; 18(1):35-9. PubMed ID: 1080036
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Familial trisomy 20p five cases and two carriers in three generations a review.
    Centerwall W; Francke U
    Ann Genet; 1977 Jun; 20(2):77-83. PubMed ID: 302689
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Partial 7 q trisomy. One or 2 syndromes? Apropos of a new case].
    Turleau C; Rossier A; de Montis G; Roubin M; Chavin-Colin F; de Grouchy J
    Ann Genet; 1976 Mar; 19(1):37-42. PubMed ID: 1084120
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Trisomy for the distal segment of the short arm of chromosome 17 in a boy with mild mental retardation and some dysmorphic features.
    Mégarbané A; Souraty N; Theophile D; Vekemans M; Samaras L; Ghorayeb Z
    Ann Genet; 1997; 40(1):55-9. PubMed ID: 9150851
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Partial trisomy of the short arm of chromosome 3. Case report and phenotype expression].
    Frankova YE; Holenova H; Braulke I
    Monatsschr Kinderheilkd; 1991 Dec; 139(12):841-3. PubMed ID: 1770961
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [The phenotype of the trisomy of the short arm of chromosome no. 4. (a new case with t (4p; 11q) (author's transl)].
    Kessel E; Pfeiffer RA; Kosenow W
    Klin Padiatr; 1976 May; 188(3):215-9. PubMed ID: 945417
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Partial trisomy of the distal part of 10q: a report of two Egyptian cases.
    Aglan MS; Kamel AK; Helmy NA
    Genet Couns; 2008; 19(2):199-209. PubMed ID: 18618995
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. An inherited translocation t(4;15) (p16;q22) leading to two cases of partial trisomy 15.
    Cohen MM; Ornoy A; Rosenmann A; Kohn G
    Ann Genet; 1975 Jun; 18(2):99-103. PubMed ID: 1081372
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Trisomy of chromosome 16p13.3 due to an unbalanced insertional translocation into chromosome 22p13.
    de Ravel T; Aerssens P; Vermeesch JR; Fryns JP
    Eur J Med Genet; 2005; 48(3):355-9. PubMed ID: 16179232
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.