BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

260 related articles for article (PubMed ID: 2817774)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. Translocation (X;9)(p11;q34) in a girl with incontinentia pigmenti (IP): implications for the regional assignment of the IP locus to Xp11?
    Gilgenkrantz S; Tridon P; Pinel-Briquel N; Beurey J; Weber M
    Ann Genet; 1985; 28(2):90-2. PubMed ID: 3876069
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Incontinentia pigmenti. Study of 3 families].
    Garcia-Bravo B; Rodriguez-Pichardo A; Camacho-Martinez F
    Ann Dermatol Venereol; 1986; 113(4):301-8. PubMed ID: 3767228
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Incontinentia pigmenti (type 1) and X;5 translocation.
    Bitoun P; Philippe C; Cherif M; Mulcahy MT; Gilgenkrantz S
    Ann Genet; 1992; 35(1):51-4. PubMed ID: 1610121
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clinical features and computer-aided analysis of chromosome aberration in a case with incontinentia pigmenti.
    Parcheta B; Skawinski W; Wisniewski L; Piontek E; Ryzko J
    Klin Padiatr; 1987; 199(1):32-6. PubMed ID: 3550261
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Incontinentia pigmenti achromians (hypomelanosis of ITO, MIM 146150): further evidence of localization at Xp11.
    Koiffmann CP; de Souza DH; Diament A; Ventura HB; Alves RS; Kihara S; Wajntal A
    Am J Med Genet; 1993 Jun; 46(5):529-33. PubMed ID: 8322815
    [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. 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]  

  • 11. 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]  

  • 12. Noninactivation of a portion of Xq28 in a balanced X-autosome translocation.
    Du Sart D; Kalitsis P; Schmidt M
    Am J Med Genet; 1992 Jan; 42(2):156-60. PubMed ID: 1733163
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Translocation (X;13)(p11.21;q12.3) in a girl with incontinentia pigmenti and bilateral retinoblastoma.
    Kajii T; Tsukahara M; Fukushima Y; Hata A; Matsuo K; Kuroki Y
    Ann Genet; 1985; 28(4):219-23. PubMed ID: 3879432
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Incontinentia pigmenti (IP) and r(X). Tentative mapping of the IP locus to the X juxtacentromeric region.
    de Grouchy J; Turleau C; Doussau de Bazignan M; Maroteaux P; Thibaud D
    Ann Genet; 1985; 28(2):86-9. PubMed ID: 3876068
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The gene for incontinentia pigmenti is assigned to Xq28.
    Sefiani A; Abel L; Heuertz S; Sinnett D; Lavergne L; Labuda D; Hors-Cayla MC
    Genomics; 1989 Apr; 4(3):427-9. PubMed ID: 2714798
    [TBL] [Abstract][Full Text] [Related]  

  • 17. X;autosome translocations in females with Duchenne or Becker muscular dystrophy.
    Dubowitz V
    Nature; 1986 Jul 17-23; 322(6076):291-2. PubMed ID: 3461282
    [No Abstract]   [Full Text] [Related]  

  • 18. Linkage analysis in 16 families with incontinentia pigmenti.
    Jouet M; Stewart H; Landy S; Yates J; Yong SL; Harris A; Garret C; Hatchwell E; Read A; Donnai D; Kenwrick S
    Eur J Hum Genet; 1997; 5(3):168-70. PubMed ID: 9272741
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Genetic counselling in carriers of reciprocal chromosomal translocations involving short arm of chromosome X.
    Panasiuk B; Usinskiené R; Kostyk E; Rybałko A; Stasiewicz-Jarocka B; Krzykwa B; Pieńkowska-Grela B; Kucinskas V; Michalova K; Midro AT
    Ann Genet; 2004; 47(1):11-28. PubMed ID: 15050871
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.