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: 6218134)

  • 1. Structural variation of chromosome 21 and symptoms of Down's syndrome.
    Rethoré MO
    Hum Genet Suppl; 1981; 2():173-82. PubMed ID: 6218134
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Partial trisomy 21. Further evidence that trisomy of band 21q22 is essential for Down's phenotype.
    Hagemeijer A; Smit EM
    Hum Genet; 1977 Aug; 38(1):15-23. PubMed ID: 143443
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Atypical Down syndrome and partial trisomy 21.
    Jenkins EC; Duncan CJ; Wright CE; Giordano FM; Wilbur L; Wisniewski K; Sklower SL; French JH; Jones C; Brown WT
    Clin Genet; 1983 Aug; 24(2):97-102. PubMed ID: 6225574
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Partial trisomy 21 (21q21 - 21q22.2)].
    Poissonnier M; Saint-Paul B; Dutrillaux B; Chassaigne M; Gruyer P; de Blignières-Strouk G
    Ann Genet; 1976 Mar; 19(1):69-73. PubMed ID: 132130
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Cystathionine beta synthase: gene dosage effect in trisomy 21.
    Chadefaux B; Rethoré MO; Raoul O; Ceballos I; Poissonnier M; Gilgenkranz S; Allard D
    Biochem Biophys Res Commun; 1985 Apr; 128(1):40-4. PubMed ID: 3157380
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Moderate Down's syndrome in three siblings having partial trisomy 21q22.2 to qter and therefore no SOD-1 excess.
    Habedank M; Rodewald A
    Hum Genet; 1982; 60(1):74-7. PubMed ID: 6210617
    [No Abstract]   [Full Text] [Related]  

  • 7. Mapping of the Down syndrome phenotype on chromosome 21 at the molecular level.
    Sinet PM; Théophile D; Rahmani Z; Chettouh Z; Blouin JL; Prieur M; Noel B; Delabar JM
    Biomed Pharmacother; 1994; 48(5-6):247-52. PubMed ID: 7999986
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [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]  

  • 9. Down's syndrome phenotype and autosomal gene inactivation in a child with presumed (X;21) de novo translocation.
    Taysi K; Sparkes RS; O'Brien TJ; Dengler DR
    J Med Genet; 1982 Apr; 19(2):144-8. PubMed ID: 6210775
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Fetal phenotype in a case of partial trisomy 21 and partial monosomy 22 detected prenatally.
    Migliorini AM; Coco R; De Negrotti TC; Sanchez JM; Castineyra G
    J Med Genet; 1981 Oct; 18(5):383-5. PubMed ID: 6460105
    [TBL] [Abstract][Full Text] [Related]  

  • 11. No significant effect of monosomy for distal 21q22.3 on the Down syndrome phenotype in "mirror" duplications of chromosome 21.
    Pangalos C; Théophile D; Sinet PM; Marks A; Stamboulieh-Abazis D; Chettouh Z; Prieur M; Verellen C; Rethoré MO; Lejeune J
    Am J Hum Genet; 1992 Dec; 51(6):1240-50. PubMed ID: 1463008
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A boy with Down's syndrome having recombinant chromosome 21 but no SOD-1 excess.
    Miyazaki K; Yamanaka T; Ogasawara N
    Clin Genet; 1987 Dec; 32(6):383-7. PubMed ID: 2963715
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Multiple chromosome aberrations in 3 generations of a family and Down's syndrome resulting from partial trisomy of chromosome 21 (q21--q22)].
    Butomo IV; Prozorova MV; Khitrikova LE
    Tsitol Genet; 1984; 18(3):223-8. PubMed ID: 6235655
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Double aneuploidy: partial trisomy 21 and XO/XXX in a family with 12/21 translocation.
    Chen H; Tyrkus M; Woolley PV
    Ann Genet; 1978 Sep; 21(3):177-80. PubMed ID: 315194
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Assignment of human phosphoribosylglycinamide synthetase locus to region 21q221.
    Chadefaux B; Allard D; Rethoré MO; Raoul O; Poissonnier M; Gilgenkrantz S; Cheruy C; Jérôme H
    Hum Genet; 1984; 66(2-3):190-2. PubMed ID: 6232198
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Partial trisomies of chromosome 21 in man. Two new observations due to translocations 19;21 and 4;21.
    Pfeiffer RA; Kessel EK; Soer KH
    Clin Genet; 1977 Mar; 11(3):207-13. PubMed ID: 138497
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Segmental trisomy of chromosome 17: a mouse model of human aneuploidy syndromes.
    Vacík T; Ort M; Gregorová S; Strnad P; Blatny R; Conte N; Bradley A; Bures J; Forejt J
    Proc Natl Acad Sci U S A; 2005 Mar; 102(12):4500-5. PubMed ID: 15755806
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Three interesting cases of Down's syndrome.
    Pérez-Castillo A; Del Mazo J; Abrisqueta JA
    Ann Genet; 1983; 26(2):123-8. PubMed ID: 6225371
    [TBL] [Abstract][Full Text] [Related]  

  • 19. YAC and cosmid FISH mapping of an unbalanced chromosomal translocation causing partial trisomy 21 and Down syndrome.
    Nadal M; Milà M; Pritchard M; Mur A; Pujals J; Blouin JL; Antonarakis SE; Ballesta F; Estivill X
    Hum Genet; 1996 Oct; 98(4):460-6. PubMed ID: 8792823
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Down's syndrome: karyotypic stability of trisomy 21 in an established lympho-blastoid cell line.
    Miyoshi I; Masuji H; Fujiwara S; Kubonishi I; Kishimoto H
    Acta Med Okayama; 1976 Dec; 30(6):403-6. PubMed ID: 138335
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.