BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

166 related articles for article (PubMed ID: 1673298)

  • 1. Linkage analysis in a large family with nonspecific X-linked mental retardation.
    Glass IA; White EM; Pope MJ; Pirrit LA; Cockburn F; Connor JM
    Am J Med Genet; 1991; 38(2-3):240-3. PubMed ID: 1673298
    [TBL] [Abstract][Full Text] [Related]  

  • 2. X-linked mental retardation syndrome with characteristic "coarse" facial appearance, brachydactyly, and short stature maps to proximal Xq.
    Carpenter NJ; Qu Y; Curtis M; Patil SR
    Am J Med Genet; 1999 Jul; 85(3):230-5. PubMed ID: 10398234
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Linkage to Xq28 in a family with nonspecific X-linked mental retardation.
    Nordström AM; Penttinen M; von Koskull H
    Hum Genet; 1992 Nov; 90(3):263-6. PubMed ID: 1362558
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Gene for non-specific X-linked mental retardation maps in the pericentromeric region.
    Samanns C; Albrecht R; Neugebauer M; Neri G; Gal A
    Am J Med Genet; 1991; 38(2-3):224-7. PubMed ID: 2018062
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Linkage of nonspecific X-linked mental retardation to Xq21.31.
    Jedele KB; Michels VV; Schaid DJ; Schowalter KV; Thibodeau SN
    Am J Med Genet; 1992 Apr 15-May 1; 43(1-2):436-42. PubMed ID: 1605223
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mapping of a gene for nonspecific X-linked mental retardation (MRX 75) to Xq24-q26.
    Caspari R; Uhlhaas S; Friedl W; Knapp M; Propping P
    Am J Med Genet; 2000 Aug; 93(4):290-3. PubMed ID: 10946355
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Gene localization in a family with X-linked syndromal mental retardation (Prieto syndrome).
    Watty A; Prieto F; Beneyto M; Neugebauer M; Gal A
    Am J Med Genet; 1991; 38(2-3):234-9. PubMed ID: 1673297
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Non-specific X linked mental retardation with aphasia exhibiting genetic linkage to chromosomal region Xp11.
    Wilson GN; Richards CS; Katz K; Brookshire GS
    J Med Genet; 1992 Sep; 29(9):629-34. PubMed ID: 1357179
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Regional localization of a nonspecific X-linked mental retardation gene (MRX59) to Xp21.2-p22.2.
    Carpenter NJ; Brown WT; Qu Y; Keenan KL
    Am J Med Genet; 1999 Jul; 85(3):266-70. PubMed ID: 10398241
    [TBL] [Abstract][Full Text] [Related]  

  • 10. MRX8: an X-linked mental retardation condition with linkage to Xq21.
    Schwartz CE; May M; Huang T; Ledbetter D; Anderson G; Barker DF; Lubs HA; Arena F; Stevenson RE
    Am J Med Genet; 1992 Apr 15-May 1; 43(1-2):467-74. PubMed ID: 1605227
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Gene for nonspecific X-linked mental retardation (MRX 47) is located in Xq22.3-q24.
    des Portes V; Soufir N; Carrié A; Billuart P; Bienvenu T; Vinet MC; Beldjord C; Ponsot G; Kahn A; Boué J; Chelly J
    Am J Med Genet; 1997 Oct; 72(3):324-8. PubMed ID: 9332663
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The fragile X syndrome in a large family. III. Investigations on linkage of flanking DNA markers with the fragile site Xq27.
    Veenema H; Carpenter NJ; Bakker E; Hofker MH; Ward AM; Pearson PL
    J Med Genet; 1987 Jul; 24(7):413-21. PubMed ID: 2886667
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Linkage studies of X-linked mental retardation: high frequency of recombination in the telomeric region of the human X chromosome (fragile site/linkage/recombination/X chromosome).
    Davies KE; Mattei MG; Mattei JF; Veenema H; McGlade S; Harper K; Tommerup N; Nielsen KB; Mikkelsen M; Beighton P
    Hum Genet; 1985; 70(3):249-55. PubMed ID: 2991115
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Waisman syndrome, a human X-linked recessive basal ganglia disorder with mental retardation: localization to Xq27.3-qter.
    Gregg RG; Metzenberg AB; Hogan K; Sekhon G; Laxova R
    Genomics; 1991 Apr; 9(4):701-6. PubMed ID: 1674730
    [TBL] [Abstract][Full Text] [Related]  

  • 15. PPM-X: a new X-linked mental retardation syndrome with psychosis, pyramidal signs, and macroorchidism maps to Xq28.
    Lindsay S; Splitt M; Edney S; Berney TP; Knight SJ; Davies KE; O'Brien O; Gale M; Burn J
    Am J Hum Genet; 1996 Jun; 58(6):1120-6. PubMed ID: 8651288
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A new syndrome with mental retardation, short stature and an Xq duplication.
    Thode A; Partington MW; Yip MY; Chapman C; Richardson VF; Turner G
    Am J Med Genet; 1988; 30(1-2):239-50. PubMed ID: 3177451
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A non-syndromal form of X-linked mental retardation (XLMR) is linked to DXS14.
    Suthers GK; Turner G; Mulley JC
    Am J Med Genet; 1988; 30(1-2):485-91. PubMed ID: 3177466
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Multipoint genetic mapping of the Xq26-q28 region in families with fragile X mental retardation and in normal families reveals tight linkage of markers in q26-q27.
    Oberlé I; Camerino G; Wrogemann K; Arveiler B; Hanauer A; Raimondi E; Mandel JL
    Hum Genet; 1987 Sep; 77(1):60-5. PubMed ID: 3502701
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A unique form of mental retardation with a distinctive phenotype maps to Xq26-q27.
    Shashi V; Berry MN; Shoaf S; Sciote JJ; Goldstein D; Hart TC
    Am J Hum Genet; 2000 Feb; 66(2):469-79. PubMed ID: 10677307
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mapping of a gene for non-specific X linked mental retardation: evidence for linkage to chromosomal region Xp21.1-Xp22.3.
    Kozák L; Chiurazzi P; Genuardi M; Pomponi MG; Zollino M; Neri G
    J Med Genet; 1993 Oct; 30(10):866-9. PubMed ID: 8230164
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.