BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

212 related articles for article (PubMed ID: 1985463)

  • 1. Localization of DNA sequences to a region within Xp11.21 between incontinentia pigmenti (IP1) X-chromosomal translocation breakpoints.
    Gorski JL; Burright EN; Harnden CE; Stein CK; Glover TW; Reyner EL
    Am J Hum Genet; 1991 Jan; 48(1):53-64. PubMed ID: 1985463
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Isolation of DNA markers from a region between incontinentia pigmenti 1 (IP1) X-chromosomal translocation breakpoints by a comparative PCR analysis of a radiation hybrid subclone mapping panel.
    Gorski JL; Burright EN; Reyner EL; Goodfellow PN; Burgess DL
    Genomics; 1992 Nov; 14(3):649-56. PubMed ID: 1427891
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A somatic cell hybrid panel to facilitate identification of DNA sequences in the vicinity of the incontinentia pigmenti locus (IP1).
    Gorski JL; Stein CK; Glover TW
    Cytogenet Cell Genet; 1989; 52(1-2):90-2. PubMed ID: 2558857
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Cosmids map two incontinentia pigmenti type 1 (IP1) translocation breakpoints to a 180-kb region within a 1.2-Mb YAC contig.
    Gorski JL; Bialecki MD; McDonald MT; Massa HF; Trask BJ; Burright EN
    Genomics; 1996 Jul; 35(2):338-45. PubMed ID: 8661147
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A radiation hybrid map of the proximal short arm of the human X chromosome spanning incontinentia pigmenti 1 (IP1) translocation breakpoints.
    Gorski JL; Boehnke M; Reyner EL; Burright EN
    Genomics; 1992 Nov; 14(3):657-65. PubMed ID: 1427892
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The molecular genetics of incontinentia pigmenti.
    Gorski JL; Burright EN
    Semin Dermatol; 1993 Sep; 12(3):255-65. PubMed ID: 8105861
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Linkage studies do not confirm the cytogenetic location of incontinentia pigmenti on Xp11.
    Sefiani A; Sinnett D; Abel L; Szpiro-Tapia S; Heuertz S; Craig I; Fraser N; Kruse TA; Frydman M; Peter MO
    Hum Genet; 1988 Nov; 80(3):282-6. PubMed ID: 3192215
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A 2-Mb YAC contig encompassing three loci (DXF34, DXS14, and DXS390) that lie between Xp11.2 translocation breakpoints associated with incontinentia pigmenti type 1.
    Reed V; Rider S; Maslen GL; Hatchwell E; Blair HJ; Uwechue IC; Craig IW; Laval SH; Monaco AP; Boyd Y
    Genomics; 1994 Apr; 20(3):341-6. PubMed ID: 8034305
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The gene for incontinentia pigmenti: failure of linkage studies using DNA probes to confirm cytogenetic localization.
    Harris A; Lankester S; Haan E; Beres J; Hulten M; Szollar J; Souttier L; Bobrow M
    Clin Genet; 1988 Jul; 34(1):1-6. PubMed ID: 2900707
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Three Finnish incontinentia pigmenti (IP) families with recombinations with the IP loci at Xq28 and Xp11.
    Hydén-Granskog C; Salonen R; von Koskull H
    Hum Genet; 1993 Mar; 91(2):185-9. PubMed ID: 8096494
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Physical mapping of the von Recklinghausen neurofibromatosis region on chromosome 17.
    Fountain JW; Wallace MR; Brereton AM; O'Connell P; White RL; Rich DC; Ledbetter DH; Leach RJ; Fournier RE; Menon AG
    Am J Hum Genet; 1989 Jan; 44(1):58-67. PubMed ID: 2491783
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Incontinentia pigmenti and X-autosome translocations. Non-isotopic in situ hybridization with an X-centromere-specific probe (pSV2X5) reveals a possible X-centromeric breakpoint in one of five published cases.
    Crolla JA; Gilgenkrantz S; de Grouchy J; Kajii T; Bobrow M
    Hum Genet; 1989 Feb; 81(3):269-72. PubMed ID: 2921037
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Assignment of human erythroid delta-aminolevulinate synthase (ALAS2) to a distal subregion of band Xp11.21 by PCR analysis of somatic cell hybrids containing X; autosome translocations.
    Cotter PD; Willard HF; Gorski JL; Bishop DF
    Genomics; 1992 May; 13(1):211-2. PubMed ID: 1577484
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Gene for incontinentia pigmenti maps to band Xp11 with an (X;10) (p11;q22) translocation.
    Cannizzaro LA; Hecht F
    Clin Genet; 1987 Jul; 32(1):66-9. PubMed ID: 3621656
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Two cases of X/autosome translocation in females with incontinentia pigmenti.
    Hodgson SV; Neville B; Jones RW; Fear C; Bobrow M
    Hum Genet; 1985; 71(3):231-4. PubMed ID: 4065895
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Recent progress in the genetics of incontinentia pigmenti (Bloch-Sulzberger syndrome).
    Shastry BS
    J Hum Genet; 2000; 45(6):323-6. PubMed ID: 11185738
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Incontinentia pigmenti: Xp breakpoint is not the same in a case of r(X) and in X/autosome translocations.
    Sefiani A; Heuertz S; Turleau C; Thibaud D; de Grouchy J; Hors-Cayla MC
    Ann Genet; 1989; 32(3):149-51. PubMed ID: 2817774
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mapping of 12 translocation breakpoints in the Xp21 region with respect to the locus for Duchenne muscular dystrophy.
    Boyd Y; Cockburn D; Holt S; Munro E; Van Ommen GJ; Gillard B; Affara N; Ferguson-Smith M; Craig I
    Cytogenet Cell Genet; 1988; 48(1):28-34. PubMed ID: 3180845
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Localization of X chromosome short arm markers relative to synovial sarcoma- and renal adenocarcinoma-associated translocation breakpoints.
    Sinke RJ; de Leeuw B; Janssen HA; Weghuis DO; Suijkerbuijk RF; Meloni AM; Gilgenkrantz S; Berger W; Ropers HH; Sandberg AA
    Hum Genet; 1993 Oct; 92(3):305-8. PubMed ID: 8406438
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Identification of the breakpoint-flanking markers on chromosomes 1 and 17 of a constitutional translocation T(1;17)(P36;Q12-21) in a patient with neuroblastoma].
    Laureys GG
    Verh K Acad Geneeskd Belg; 1995; 57(5):389-422. PubMed ID: 8571670
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.