BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

212 related articles for article (PubMed ID: 7381872)

  • 1. Ring chromosome 10:46,XX,r(10)(p15 leads to q26).
    Tsukino R; Tsuda N; Dezawa T; Ishii T; Koike M
    J Med Genet; 1980 Apr; 17(2):148-50. PubMed ID: 7381872
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Ring-G chromosome, a new G-deletion syndrome?
    Weleber RG; Hecht F; Giblett ER
    Am J Dis Child; 1968 Apr; 115(4):489-93. PubMed ID: 4296014
    [No Abstract]   [Full Text] [Related]  

  • 4. Familial mental retardation in a family with an inherited chromosome rearrangement.
    Chudley AE; Bauder F; Ray M; McAlpine PJ; Pena SD; Hamerton JL
    J Med Genet; 1974 Dec; 11(4):353-66. PubMed ID: 4140909
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Syndrome associated with a deficiency of part of the long arm of chromosome no. 18.
    Insley J
    Arch Dis Child; 1967 Apr; 42(222):140-6. PubMed ID: 4381584
    [No Abstract]   [Full Text] [Related]  

  • 6. The 4p-syndrome, with a report of two new cases.
    Fryns JP; Eggermont E; Verresen H; Van den Berghe H
    Humangenetik; 1973; 19(1):99-109. PubMed ID: 4725911
    [No Abstract]   [Full Text] [Related]  

  • 7. Ring chromosome 6: case report and review of literature.
    Kini KR; Van Dyke DL; Weiss L; Logan MS
    Hum Genet; 1979; 50(2):145-9. PubMed ID: 511129
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A ring chromosome, diagnosed by quinacrine fluorescence as No. 9, in a mentally retarded girl.
    Jacobsen P; Mikkelsen M; Rosleff F
    Clin Genet; 1973; 4(5):434-41. PubMed ID: 4127395
    [No Abstract]   [Full Text] [Related]  

  • 9. A child with a ring-4 chromosome (46,XX-46,XX,r 4).
    Parker CE; Alfi OS; Derencsenyi A; Mavalwala J; Donnell G
    Am J Dis Child; 1974 Sep; 128(3):371-4. PubMed ID: 4411581
    [No Abstract]   [Full Text] [Related]  

  • 10. An (11;21) translocation in four generations with chromosome 11 abnormalities in the offspring. A clinical, cytogenetical, and gene marker study.
    Jacobsen P; Hauge M; Henningsen K; Hobolth N; Mikkelsen M; Philip J
    Hum Hered; 1973; 23(6):568-85. PubMed ID: 4134631
    [No Abstract]   [Full Text] [Related]  

  • 11. Ring chromosome 8 in a boy with multiple congenital abnormalities and mental retardation.
    Hamers AJ; van Kempen C
    J Med Genet; 1977 Dec; 14(6):451-5. PubMed ID: 604497
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Two cases of ring chromosome 11.
    Romain DR; Gebbie OB; Parfitt RG; Columbano-Green LM; Smythe RH; Chapman CJ; Kerr A
    J Med Genet; 1983 Oct; 20(5):380-2. PubMed ID: 6315941
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Trisomy for the short arms of chromosome 9 in two generations, with balanced translocations t(15pplus;9qminus) in three generations.
    Podruch PE; Weisskopf B
    J Pediatr; 1974 Jul; 85(1):92-5. PubMed ID: 4855265
    [No Abstract]   [Full Text] [Related]  

  • 14. Developmental abnormalities in a patient with karyotype 46,XX,bq+.
    Chakanovskis JE; Sutherland GR
    J Med Genet; 1970 Jun; 7(2):180-4. PubMed ID: 5519607
    [No Abstract]   [Full Text] [Related]  

  • 15. [Giemsa-R-banding analysis of the trisomy 9p and report of a new case].
    Rethoré MO; Hoehn H; Rott HD; Couturier J; Dutrillaux B; Lejeune J
    Humangenetik; 1973 Apr; 18(2):129-38. PubMed ID: 4124236
    [No Abstract]   [Full Text] [Related]  

  • 16. A 13-year-old girl with Wolf's syndrome and karyotype 46,XX,del(4)(pter integral p15::p12 integral qter),9qh+. Increased risk of structural chromosome abnormalities in the progeny of mothers with 9qh+.
    Nielsen J; Fischer O; Rasmussen K; Sillesen I; Bernsen A; Saldaña-Garcia P
    J Ment Defic Res; 1977 Jun; 21(2):119-26. PubMed ID: 894706
    [No Abstract]   [Full Text] [Related]  

  • 17. Chromosomal abnormalities in a girl with physical and mental maldevelopment.
    Subrt I; Hníková O
    Hum Hered; 1970; 20(3):252-9. PubMed ID: 5489883
    [No Abstract]   [Full Text] [Related]  

  • 18. 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]  

  • 19. Ring chromosome 13 syndrome.
    Fried K; Rosenblatt M; Mundel G; Krikler R
    Clin Genet; 1975 Mar; 7(3):203-8. PubMed ID: 1139790
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Ring 1 chromosome and dwarfism--a possible syndrome.
    Wolf CB; Peterson JA; LoGrippo GA; Weiss L
    J Pediatr; 1967 Nov; 71(5):719-22. PubMed ID: 6054759
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 11.