BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

132 related articles for article (PubMed ID: 2872982)

  • 1. Deleted ring chromosome 22 in a mentally retarded boy.
    Gustavson KH; Arancibia W; Eriksson U; Svennerholm L
    Clin Genet; 1986 Apr; 29(4):337-41. PubMed ID: 2872982
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Conserved autosomal syntenic group on mouse (MMU) chromosome 15 and human (HSA) chromosome 22: assignment of a gene for arylsulfatase A to MMU 15 and regional mapping of DIA1, ARSA, and ACO2 on HSA 22.
    Francke U; Tetri P; Taggart RT; Oliver N
    Cytogenet Cell Genet; 1981; 31(2):58-69. PubMed ID: 6118238
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Deletions of proximal 15q and non-classical Prader-Willi syndrome phenotypes.
    Schwartz S; Max SR; Panny SR; Cohen MM
    Am J Med Genet; 1985 Feb; 20(2):255-63. PubMed ID: 2858158
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Ring chromosome 4.
    McDermott A; Voyce MA; Romain D
    J Med Genet; 1977 Jun; 14(3):228-32. PubMed ID: 881718
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Regional localization of the genes coding for human ACO2, ARSA, and NAGA on chromosome 22.
    Geurts van Kessel AH; Westerveld A; de Groot PG; Meera Khan P; Hagemeijer A
    Cytogenet Cell Genet; 1980; 28(3):169-72. PubMed ID: 7192199
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Confirmation of the assignment of the gene for arylsulfatase A to chromosome 22 using somatic cell hybrids.
    Hors-Cayla MC; Heuertz S; Van Cong N; Weil D; Frézal J
    Hum Genet; 1979 May; 49(1):33-9. PubMed ID: 38202
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Partial trisomy 22q with elevated arylsulfatase-A activity.
    Fryns JP; Jaeken J; van den Berghe H
    Ann Genet; 1979; 22(3):168-70. PubMed ID: 43111
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Gene dosage effect for beta-glucuronidase (GUSB) in monosomy 7 cells of patients with myeloproliferative disorders.
    Danesino C; Pasquali F
    Acta Anthropogenet; 1983; 7(2):133-42. PubMed ID: 6146321
    [TBL] [Abstract][Full Text] [Related]  

  • 9. X;15 translocation in a retarded girl: X inactivation pattern and attempt to localise the hexosaminidase A and other loci.
    Bernstein R; Dawson B; Kohl R; Jenkins T
    J Med Genet; 1979 Aug; 16(4):254-62. PubMed ID: 290816
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A case of partial monosomy 21q22.2 associated with Rieger's syndrome.
    Nielsen F; Trånebjaerg L
    J Med Genet; 1984 Jun; 21(3):218-21. PubMed ID: 6431108
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Cytogenetic, biochemical, and molecular analyses of a 22q13 deletion.
    Phelan MC; Thomas GR; Saul RA; Rogers RC; Taylor HA; Wenger DA; McDermid HE
    Am J Med Genet; 1992 Jul; 43(5):872-6. PubMed ID: 1353666
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Expression of human arylsulfatase-A in man-hamster somatic cell hybrids.
    Bruns GA; Mintz BJ; Leary AC; Regina VM; Gerald PS
    Cytogenet Cell Genet; 1978; 22(1-6):182-5. PubMed ID: 37046
    [No Abstract]   [Full Text] [Related]  

  • 13. Unusual X chromosome inactivation in a mentally retarded girl with an interstitial deletion Xq27: implications for the fragile X syndrome.
    Schmidt M; Certoma A; Du Sart D; Kalitsis P; Leversha M; Fowler K; Sheffield L; Jack I; Danks DM
    Hum Genet; 1990 Mar; 84(4):347-52. PubMed ID: 2307456
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A deleted extra chromosome 22 identified by DNA replication banding.
    Parslow M; Hoo JJ; Garry M; Rose F
    Hum Genet; 1980; 53(3):323-6. PubMed ID: 7372336
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Regional assignment of arylsulfatase A, mitochondrial aconitase and NADH-cytochrome b5 reductase by somatic cell hybridization.
    Hors-Cayla MC; Junien C; Heuertz S; Mattei JF; Frézal J
    Hum Genet; 1981; 58(2):140-3. PubMed ID: 6116664
    [No Abstract]   [Full Text] [Related]  

  • 16. Terminal 22q deletion associated with a partial deficiency of arylsulphatase A.
    Narahara K; Takahashi Y; Murakami M; Tsuji K; Yokoyama Y; Murakami R; Ninomiya S; Seino Y
    J Med Genet; 1992 Jun; 29(6):432-3. PubMed ID: 1352356
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A cytogenetic survey of an institution for the mentally retarded: I. Chromosome abnormalities.
    Jacobs PA; Matsuura JS; Mayer M; Newlands IM
    Clin Genet; 1978 Jan; 13(1):37-60. PubMed ID: 146575
    [TBL] [Abstract][Full Text] [Related]  

  • 18. High resolution pattern of an inverted duplication (15).
    Hoo JJ
    Clin Genet; 1986 Mar; 29(3):241-5. PubMed ID: 3457663
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular analysis redefines three human chromosome 14 deletions.
    Wintle RF; Costa T; Haslam RH; Teshima IE; Cox DW
    Hum Genet; 1995 May; 95(5):495-500. PubMed ID: 7759068
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A bisatellited marker chromosome in a mentally retarded girl with infantile autism.
    Rasmussen K; Nielsen J; Sillesen I; Brask BH; Saldaña-Garcia P
    Hereditas; 1976; 82(1):37-42. PubMed ID: 1262237
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.