BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

196 related articles for article (PubMed ID: 159858)

  • 1. Down's syndrome in brother and sister without evident trisomy 21.
    Parloir C; Fryns JP; Van den Berghe H
    Hum Genet; 1979 Oct; 51(2):227-30. PubMed ID: 159858
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Report on a case of Down's syndrome with mosaicism. Trisomy 21-normal, clearly mongoloid phenotype and normal iliac index in a newborn infant].
    De Prà M; Lunetta Q
    Minerva Pediatr; 1974 Jan; 26(2):78-81. PubMed ID: 4276194
    [No Abstract]   [Full Text] [Related]  

  • 3. [Mosaicism-trisomy in fathers of two children with Down's syndrome].
    Domány Z; Métneki J
    Acta Paediatr Acad Sci Hung; 1976; 17(3):177-81. PubMed ID: 141192
    [No Abstract]   [Full Text] [Related]  

  • 4. Paternal trisomy 21 mosaicism and Down's syndrome.
    Hsu LY; Gertner M; Leiter E; Hirschhorn K
    Am J Hum Genet; 1971 Nov; 23(6):592-601. PubMed ID: 4257130
    [No Abstract]   [Full Text] [Related]  

  • 5. Down's syndrome transmitted through maternal mosaicism.
    Aarskog D
    Acta Paediatr Scand; 1969 Nov; 58(6):609-14. PubMed ID: 4244880
    [No Abstract]   [Full Text] [Related]  

  • 6. Trisomy 21 mosaicism in a woman with two children with trisomy 21 Down's syndrome.
    Kaffe S; Hsu LY; Hirschhorn K
    J Med Genet; 1974 Dec; 11(4):378-9. PubMed ID: 4140911
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Trisomy 21 with 47,+18 lymphocyte cell line: double mitotic nondisjunction.
    Jenkins MB; Kriel RL; Boyd L; Barnwell A
    J Med Genet; 1978 Oct; 15(5):395-8. PubMed ID: 153975
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Cytogenetic studies of a family with trisomy 21 mosaicism in two successive generations as the cause of Down's syndrome.
    Werner W; Herrmann FH; John B
    Hum Genet; 1982; 60(2):202-4. PubMed ID: 6210621
    [No Abstract]   [Full Text] [Related]  

  • 9. [Down's syndrome with confirmation of trisomy G solely in fibroblast cultures].
    Haberlandt W
    J Genet Hum; 1973 Sep; 21(3):215-22. PubMed ID: 4282491
    [No Abstract]   [Full Text] [Related]  

  • 10. [Down's syndrome with predominantly normal karyotype in lymphocyte culture but extensive G trisomy in fibroblast culture].
    Haberlandt W; Wunderlich C
    Arztl Forsch; 1972 Sep; 26(9):309-16. PubMed ID: 4262890
    [No Abstract]   [Full Text] [Related]  

  • 11. Trisomy 18 and trisomy 21 mosaicism in a Down's syndrome patient.
    Thomas IM; Sayee R; Shavanthi L; Sridevi H
    J Med Genet; 1994 May; 31(5):418-9. PubMed ID: 8064824
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A family with three sibs carrying trisomy 21.
    Nuzzo F; Stefanini M; Simoni G; Larizza L; Mottura A; Reali E; Franceschini P
    Ann Genet; 1975 Jun; 18(2):111-6. PubMed ID: 127545
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The importance of chromosome analysis in Down's syndrome. A case report of a 21-21 translocation.
    Eber LM; Goodman RM
    Ohio State Med J; 1966 Jan; 62(1):40-3. PubMed ID: 4232315
    [No Abstract]   [Full Text] [Related]  

  • 14. Letter: Paternal origin of the extra chromosome in Down's syndrome.
    Lancet; 1973 Dec; 2(7840):1257-8. PubMed ID: 4128576
    [No Abstract]   [Full Text] [Related]  

  • 15. Down's syndrome in Western Australia: cytogenetics and incidence.
    Mulcahy MT
    Hum Genet; 1979 Apr; 48(1):67-72. PubMed ID: 156692
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Secondary nondisjunction causing regular trisomy 21 in the offspring of a mosaic trisomy 21 mother.
    Krmpotic E; Hardin MB
    Am J Obstet Gynecol; 1971 Jun; 110(4):589-90. PubMed ID: 4253289
    [No Abstract]   [Full Text] [Related]  

  • 17. [Cytogenetic studies in children with Down's syndrome and in their relatives].
    Ostojska J
    Pediatr Pol; 1972 Oct; 47(10):1231-8. PubMed ID: 4263834
    [No Abstract]   [Full Text] [Related]  

  • 18. Parental dermatoglyphics in Down's syndrome. A ten-year study.
    Priest JH; Verhulst C; Sirkin S
    J Med Genet; 1973 Dec; 10(4):328-32. PubMed ID: 4272738
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Karyotypic analysis of 150 cases of Down's Syndrome in Iraq.
    Ferman A; Shakir A
    J Ment Defic Res; 1976 Jun; 20(2):83-7. PubMed ID: 133247
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Significance of the type of chromosome aberrations and biochemical disorders for diagnosis of Down's syndrome and the phenotype of partial trisomy 21].
    Mikiel-Kostyra K; Czerski P; Bartosz G; Sito A; Leyka W
    Pediatr Pol; 1980 Jan; 55(1):23-32. PubMed ID: 6445053
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 10.