BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

167 related articles for article (PubMed ID: 4142590)

  • 1. The supernumerary isochromosome 18 syndrome (+ 18pu).
    Condron CJ; Cantwell RJ; Kaufman RL; Brown SB; Warren RJ
    Birth Defects Orig Artic Ser; 1974; 10(10):36-42. PubMed ID: 4142590
    [No Abstract]   [Full Text] [Related]  

  • 2. A short, retarded child with a deletion of the short arm of chromosome 18 (18p-).
    Parker CE; Donnell GN; Mavalwala J; Hurst N; Derencsenyi A
    Clin Pediatr (Phila); 1973 Jan; 12(1):42-6. PubMed ID: 4345621
    [No Abstract]   [Full Text] [Related]  

  • 3. Trisomy 18.
    James AE; Belcourt CL; Atkins L; Janower ML
    Radiology; 1969 Jan; 92(1):37-43. PubMed ID: 4236175
    [No Abstract]   [Full Text] [Related]  

  • 4. An inherited small extra chromosome: a mother with 46,XX,t(17;22)(pl;ql) and a son with 47,XY,+der(22)mat.
    Borgaonkar DS; McKusick VA; Farber PA
    J Med Genet; 1973 Dec; 10(4):379-84. PubMed ID: 4129973
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Aneusomy by recombination: a possible example involving the E18 chromosome.
    Richardson HB; Bartalos M
    Acta Genet Med Gemellol (Roma); 1969 Apr; 18(2):117-24. PubMed ID: 5364594
    [No Abstract]   [Full Text] [Related]  

  • 6. Dicentric chromosome due to an unusual fusion.
    Subrt I; Blehová B; Táborský O
    Humangenetik; 1971; 12(2):136-41. PubMed ID: 5568732
    [No Abstract]   [Full Text] [Related]  

  • 7. Familial occurrence of 18q.
    Subrt I; Pokorný J
    Humangenetik; 1970 Sep; 10(2):181-7. PubMed ID: 5507053
    [No Abstract]   [Full Text] [Related]  

  • 8. A mentally retarded boy with multiple congenital anomalies and aberrant morphology in a no. 18 chromosome.
    Van Kempen C
    Dev Med Child Neurol; 1967 Oct; 9(5):617-24. PubMed ID: 6066027
    [No Abstract]   [Full Text] [Related]  

  • 9. Immunoglobulin abnormality in a girl with a large chromosome 18.
    Yanagisawa S
    J Med Genet; 1972 Sep; 9(3):360-5. PubMed ID: 4116772
    [No Abstract]   [Full Text] [Related]  

  • 10. [The clinical features of the 18 q-syndrome (author's transl)].
    Feichtinger C; Glatzl J
    Wien Klin Wochenschr; 1974 Aug; 86(15):441-4. PubMed ID: 4605988
    [No Abstract]   [Full Text] [Related]  

  • 11. Clinical aspects of chromosome aberrations.
    Dutrillaux B; Lejeune J
    Triangle; 1972; 11(3):81-9. PubMed ID: 4656754
    [No Abstract]   [Full Text] [Related]  

  • 12. Clinical experience with trisomies 18 and 13.
    Hodes ME; Cole J; Palmer CG; Reed T
    J Med Genet; 1978 Feb; 15(1):48-60. PubMed ID: 637922
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Identification of chromosomal abnormalities by quinacrine-staining technique in patients with normal karyotypes by conventional analysis.
    del Solar C; Uchida IA
    J Pediatr; 1974 Apr; 84(4):534-8. PubMed ID: 4134885
    [No Abstract]   [Full Text] [Related]  

  • 14. Developmental delay caused by a supernumerary chromosome, inv dup (15), identified by fluorescent in situ hybridization.
    Abuelo D; Mark HF; Bier JA
    Clin Pediatr (Phila); 1995 Apr; 34(4):223-6. PubMed ID: 7540523
    [No Abstract]   [Full Text] [Related]  

  • 15. [The deletion of the short arm of chromosome 18 (18p- syndrome), apropos of a new observation].
    Gilgenkrantz S; Marchal C; Neimann N
    Ann Genet; 1968 Mar; 11(1):17-21. PubMed ID: 5301751
    [No Abstract]   [Full Text] [Related]  

  • 16. [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]  

  • 17. [18 p-syndrome and hypothyroidism].
    Battin J; Serville F; Marchand JC
    Arch Fr Pediatr; 1973 May; 30(5):548. PubMed ID: 4733656
    [No Abstract]   [Full Text] [Related]  

  • 18. A possible case of trisomy 22.
    Chaudhuri A; Chandra RK; Kaul KK; Dabke AT; Chaudhuri KC
    J Ment Defic Res; 1968 Sep; 12(3):177-86. PubMed ID: 5722466
    [No Abstract]   [Full Text] [Related]  

  • 19. [Pericentric inversion of chromosome 4 : inv (4) (p13, q35) and trisomy of the short branch of chromosome 4 due to recombination aneusomy].
    Dallapiccola B; Capra L; Preto G; Covic M; Dutrillaux B
    Ann Genet; 1974 Jun; 17(2):115-8. PubMed ID: 4547938
    [No Abstract]   [Full Text] [Related]  

  • 20. The syndrome associated with the partial deletion of the long arms of chromosome 18 (18q-).
    Parker CE; Mavalwala J; Koch R; Hatashita A; Derencsenyi A
    Calif Med; 1972 Oct; 117(4):65-71. PubMed ID: 5075725
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.