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 *

139 related articles for article (PubMed ID: 885554)

  • 1. Deletion long arm 13.
    Nielsen J; Homma A; Christiansen F; Rasmussen K; Saldaña-Garcia P
    Hum Genet; 1977 Jul; 37(3):339-45. PubMed ID: 885554
    [No Abstract]   [Full Text] [Related]  

  • 2. Inherited partial duplication of chromosome No. 15.
    Fujimoto A; Towner JW; Ebbin AJ; Kahlstrom EJ; Wilson MG
    J Med Genet; 1974 Sep; 11(3):287-91. PubMed ID: 4139262
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Microcephaly, mental retardation and hypertelorism in chromosome deletion studies.
    Miller JQ
    Neurology; 1973 Nov; 23(11):1141-6. PubMed ID: 4795737
    [No Abstract]   [Full Text] [Related]  

  • 4. Retinoblastoma and deletion D (14) syndrome.
    Wilson MG; Melnyk J; Towner JW
    J Med Genet; 1969 Sep; 6(3):322-7. PubMed ID: 5345106
    [No Abstract]   [Full Text] [Related]  

  • 5. Developmental abnormalities associated with a ring chromosome 6.
    Moore CM; Heller RH; Thomas GH
    J Med Genet; 1973 Sep; 10(3):299-303. PubMed ID: 4774541
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Comparative behavior of ring chromosomes.
    Kistenmacher ML; Punnett HH
    Am J Hum Genet; 1970 May; 22(3):304-18. PubMed ID: 5445002
    [No Abstract]   [Full Text] [Related]  

  • 7. [A case of bilateral retinoblastoma with monosomy 13 (q12 leads to 114) (author's transl)].
    Walbaum R; François P; Farriaux JP; Woillez M
    Hum Genet; 1978 Oct; 44(2):219-26. PubMed ID: 730167
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Familial deletion of the short arm of the D1-chromosome (46, XX, 13 p-) not associated with loss of haptoglobin or catalase activity.
    Parker CE; Koch R; Mavalwala J; Derencsenyi A; Hatashita A
    Clin Pediatr (Phila); 1969 Aug; 8(8):453-8. PubMed ID: 5797429
    [No Abstract]   [Full Text] [Related]  

  • 9. [Enlargement of the short arm region of a small acrocentric chromosome].
    Vormittag W; Kühböck J; Weninger M
    Humangenetik; 1972; 14(2):112-21. PubMed ID: 5026841
    [No Abstract]   [Full Text] [Related]  

  • 10. Partial F trisomy associated with familial F-13 translocation detected and identified by parental chromosome studies.
    Carrel RE; Sparkes RS; Wright SW
    J Pediatr; 1971 Apr; 78(4):664-72. PubMed ID: 5547823
    [No Abstract]   [Full Text] [Related]  

  • 11. Choanal atresia and bifid thumb associated with an abnormal D group chromosome.
    Carter CH; Smith GF; Schindeler J
    J Ment Defic Res; 1970 Sep; 14(3):221-6. PubMed ID: 5518407
    [No Abstract]   [Full Text] [Related]  

  • 12. [Chromosome 18 long arm deletion. A case with unusual dermatoglyphics].
    Le Marec B; Lessard M; Renault A; Coutel Y
    Pediatrie; 1971; 26(7):749-57. PubMed ID: 5118994
    [No Abstract]   [Full Text] [Related]  

  • 13. Familial translocation involving chromosomes 6, 14 and 20, identified by quinacrine fluorescence.
    Allderdice PW; Miller OJ; Miller DA; Breg WR; Gendel E; Zelson C
    Humangenetik; 1971; 13(3):205-9. PubMed ID: 5114675
    [No Abstract]   [Full Text] [Related]  

  • 14. Chromosome 15 abnormality in a mentally retarded adult.
    Kelly S; Almy R; Dagle A
    J Med Genet; 1969 Dec; 6(4):438-41. PubMed ID: 5365954
    [No Abstract]   [Full Text] [Related]  

  • 15. Deletion 14q and pericentric inversion 14.
    Nielsen J; Homma A; Rasmussen K; Ried E; Sorensen K; Saldana-Garcia P
    J Med Genet; 1978 Jun; 15(3):236-8. PubMed ID: 671492
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Interstitial deletion of the long arm of chromosome 7 in a female child with leprechaunism].
    Ayraud N; Rovinski J; Lambert JC; Galiana A
    Ann Genet; 1976 Dec; 19(4):265-8. PubMed ID: 797303
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Partial deletion of the long arm of a group D (13-15) chromosome :Dq-].
    Laurent C; Cotton JB; Nivelon A; Freycon MT
    Ann Genet; 1967 Mar; 10(1):25-31. PubMed ID: 5300123
    [No Abstract]   [Full Text] [Related]  

  • 18. A family with a chromosome 14 short arm deletion.
    Nielsen J; Hreidarsson AB; Brynjolfsson T; Holm V; Madsen AM; Petersen GB; Lamm L; Saldańa-Garcia P
    Hereditas; 1978; 88(1):107-12. PubMed ID: 649416
    [No Abstract]   [Full Text] [Related]  

  • 19. [The chromosome 13 in ring syndrome].
    Giraud F; Emberger JM; Pinsard N; Mattei JF; Mattei MG
    Pediatrie; 1975 Jun; 30(4):339-49. PubMed ID: 1178264
    [No Abstract]   [Full Text] [Related]  

  • 20. Autosomal deletion syndrome 46,XX,18p-: a new case report with absence of IgA in serum.
    Fischer P; Golob E; Friedrich F; Kunze-Mühl E; Doleschel W; Aichmair H
    J Med Genet; 1970 Mar; 7(1):91-8. PubMed ID: 5480972
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.