BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

185 related articles for article (PubMed ID: 6846405)

  • 1. Brief clinical report: two children with de novo del(9p).
    Young RS; Bader P; Palmer CG; Kaler SG; Hodes ME
    Am J Med Genet; 1983 Apr; 14(4):751-7. PubMed ID: 6846405
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The 9p- syndrome.
    Alfi OS; Donnell GN; Allderdice PW; Derencsenyi A
    Ann Genet; 1976 Mar; 19(1):11-6. PubMed ID: 1084115
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Diagnostic hand anomalies in Smith-Magenis syndrome: four new patients with del (17)(p11.2p11.2).
    Kondo I; Matsuura S; Kuwajima K; Tokashiki M; Izumikawa Y; Naritomi K; Niikawa N; Kajii T
    Am J Med Genet; 1991 Nov; 41(2):225-9. PubMed ID: 1785639
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Brief cytogenetic case report: a 4.5-year-old girl with deletion 4q syndrome--de novo, 46,XX, del(4) (pter leads to q31:).
    Young RS; Palmer CG; Bender HA; Weaver DD; Hodes ME
    Am J Med Genet; 1982 May; 12(1):103-7. PubMed ID: 7091193
    [No Abstract]   [Full Text] [Related]  

  • 5. Interstitial deletion of (17)(p11.2p11.2): report of six additional patients with a new chromosome deletion syndrome.
    Stratton RF; Dobyns WB; Greenberg F; DeSana JB; Moore C; Fidone G; Runge GH; Feldman P; Sekhon GS; Pauli RM
    Am J Med Genet; 1986 Jul; 24(3):421-32. PubMed ID: 3728561
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Deletions of the long arm of chromosome 10.
    Shapiro SD; Hansen KL; Pasztor LM; DiLiberti JH; Jorgenson RJ; Young RS; Moore CM
    Am J Med Genet; 1985 Jan; 20(1):181-96. PubMed ID: 3970071
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Deletion 11q23-->qter (Jacobsen syndrome). Report of three new patients.
    Obregon MG; Mingarelli R; Digilio MC; Zelante L; Giannotti A; Sabatino G; Dallapiccola B
    Ann Genet; 1992; 35(4):208-12. PubMed ID: 1296516
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A clinical syndrome associated with 5p duplication and 9p deletion.
    Liberfarb RM; Atkins L; Holmes LB
    Ann Genet; 1980; 23(1):26-30. PubMed ID: 6965836
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Deletions of the long arm of chromosome 6: two new cases and review of the literature.
    Young RS; Fidone GS; Reider-Garcia PA; Hansen KL; McCombs JL; Moore CM
    Am J Med Genet; 1985 Jan; 20(1):21-9. PubMed ID: 3881954
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Partial 9p monosomy--a case with hypothyroidism.
    Ioan D; Dumitriu L; Muşeţeanu P; Bereliuc L; Belengeanu V; Maximilian C
    Endocrinologie; 1985; 23(4):279-81. PubMed ID: 4089505
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A case of partial 9p monosomy with some unusual clinical features.
    Rutten FJ; Hustinx TW; Dunk-Tillemans AA; Scheres JM; Tjon YS
    Ann Genet; 1978 Mar; 21(1):51-5. PubMed ID: 308344
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The 9p--syndrome.
    Alfi OS; Donnell GN; Derencsenyi A
    Birth Defects Orig Artic Ser; 1976; 12(5):157-60. PubMed ID: 953217
    [No Abstract]   [Full Text] [Related]  

  • 13. Deficiency of chromosome 8p21.1----8pter: case report and review of the literature.
    Dobyns WB; Dewald GW; Carlson RO; Mair DD; Michels VV
    Am J Med Genet; 1985 Sep; 22(1):125-34. PubMed ID: 3901750
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Deletion 2q37: an identifiable clinical syndrome with mental retardation and autism.
    Galasso C; Lo-Castro A; Lalli C; Nardone AM; Gullotta F; Curatolo P
    J Child Neurol; 2008 Jul; 23(7):802-6. PubMed ID: 18658079
    [TBL] [Abstract][Full Text] [Related]  

  • 15. An additional case of 9p syndrome.
    Latos-Bielenska A; Krawczynski M; Ignys I; Wolnik-Brzozowska D
    Acta Anthropogenet; 1983; 7(4):391-5. PubMed ID: 6680318
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A patient with an interstitial deletion of the proximal portion of the long arm of chromosome 4.
    Beall MH; Falk RE; Ying KL
    Am J Med Genet; 1988 Nov; 31(3):553-7. PubMed ID: 3067576
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Kabuki make-up (Niikawa-Kuroki) syndrome in five Spanish children.
    Galán-Gómez E; Cardesa-García JJ; Campo-Sampedro FM; Salamanca-Maesso C; Martínez-Frías ML; Frías JL
    Am J Med Genet; 1995 Nov; 59(3):276-82. PubMed ID: 8599349
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 46, Del (9) (22:), a new deletion syndrome.
    Alfi OS; Sanger RG; Sweeny AE; Donnell GN
    Birth Defects Orig Artic Ser; 1974; 10(8):27-34. PubMed ID: 4458825
    [No Abstract]   [Full Text] [Related]  

  • 19. Long arm deletion of chromosome 13 with exclusion of esterase D from 13q32 leads to 13qter.
    Telfer MA; Clark CE; Casey PA; Cowell HR; Stroud HH
    Clin Genet; 1980 Jun; 17(6):428-32. PubMed ID: 7398115
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Brief clinical report: interstitial deletion of the long arm of chromosome 4, del(4)(q28-->q31.3).
    Copelli S; del Rey G; Heinrich J; Coco R
    Am J Med Genet; 1995 Jan; 55(1):77-9. PubMed ID: 7702102
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.