BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

131 related articles for article (PubMed ID: 3195282)

  • 1. [A combination of Duchenne's progressive muscular dystrophy with congenital ichthyosis--a deletion or 2 independent gene mutations at Xp21--Xp22?].
    Badalian LO; Temin PA; Kamennykh LN; Zavadenko NN; Arkhipov BA
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1988; 88(8):48-51. PubMed ID: 3195282
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Duchenne's muscular dystrophy in a girl with 45,X/46,XX chromosomal mosaicism].
    Aver'ianov IuN; Bogomazov EA; Logunova LV
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1977; 77(10):1449-52. PubMed ID: 930487
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Turner's syndrome and Duchenne muscular dystrophy in a girl with an X; autosome translocation.
    Bjerglund Nielsen L; Nielsen IM
    Ann Genet; 1984; 27(3):173-7. PubMed ID: 6334482
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Xp21/autosome translocations. Case report and risk for Duchenne muscular dystrophy.
    Holden JJ; Smith A; MacLeod PM; Masotti R; Duncan AM
    Clin Genet; 1986 Jun; 29(6):516-22. PubMed ID: 3742857
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. [Molecular biology of Duchenne's muscular dystrophy].
    Coral-Vázquez R; Salamanca-Gómez F
    Gac Med Mex; 1996; 132(2):221-2. PubMed ID: 8964357
    [No Abstract]   [Full Text] [Related]  

  • 7. Aland Island eye disease (Forsius-Eriksson ocular albinism) and an Xp21 deletion in a patient with Duchenne muscular dystrophy, glycerol kinase deficiency, and congenital adrenal hypoplasia.
    Pillers DA; Weleber RG; Powell BR; Hanna CE; Magenis RE; Buist NR
    Am J Med Genet; 1990 May; 36(1):23-8. PubMed ID: 2159212
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Present-day clinico-genetic framework of Duchenne's muscular dystrophy].
    Meola G
    Riv Neurol; 1989; 59(1):8-14. PubMed ID: 2669113
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A study of Duchenne's muscular dystrophy in females. A clinical, biochemical, pathological and chromosomal study of two families.
    Reddy MV; Prabhakar V; Sadasivan G; Ebenezer LN
    Neurol India; 1968; 16(2):41-5. PubMed ID: 5682570
    [No Abstract]   [Full Text] [Related]  

  • 10. [Clinical polymorphism and genetic heterogeneity in Duchenne's progressive muscular dystrophy in girls (a review)].
    Zavadenko NN; Temin PA; Malygina NA
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1988; 88(11):123-6. PubMed ID: 3066079
    [No Abstract]   [Full Text] [Related]  

  • 11. Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene.
    Monaco AP; Neve RL; Colletti-Feener C; Bertelson CJ; Kurnit DM; Kunkel LM
    Nature; 1986 Oct 16-22; 323(6089):646-50. PubMed ID: 3773991
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The mapping of a cDNA from the human X-linked Duchenne muscular dystrophy gene to the mouse X chromosome.
    Brockdorff N; Cross GS; Cavanna JS; Fisher EM; Lyon MF; Davies KE; Brown SD
    Nature; 1987 Jul 9-15; 328(6126):166-8. PubMed ID: 3600793
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Detection of the cause of genetic fault in Duchenne's dystrophy].
    Palotie L; Somer H
    Duodecim; 1988; 104(20):1588-96. PubMed ID: 3056698
    [No Abstract]   [Full Text] [Related]  

  • 14. Theoretical expectations for deletional mutations in Duchenne muscular dystrophy.
    Grimm T; Danieli GA; Muller CR
    Am J Med Genet; 1988 Feb; 29(2):445-51. PubMed ID: 3354618
    [No Abstract]   [Full Text] [Related]  

  • 15. [Contiguous gene deletion syndrome in Xp21: the association between glycerol kinase deficiency, congenital suprarenal hypoplasia and Duchenne's muscular dystrophy].
    Pantoja-Martínez J; Martínez-Castellano F; Tarazona-Casany I; Buesa-Ibáñez E; Ardid-Encinar M; Esparza-Sánchez MA; Bonet-Arzo J
    Rev Neurol; 2007 May 16-31; 44(10):606-9. PubMed ID: 17523119
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Localization of the region homologous to the Duchenne muscular dystrophy locus on the mouse X chromosome.
    Heilig R; Lemaire C; Mandel JL; Dandolo L; Amar L; Avner P
    Nature; 1987 Jul 9-15; 328(6126):168-70. PubMed ID: 3600794
    [TBL] [Abstract][Full Text] [Related]  

  • 17. X chromosome in Duchenne muscular dystrophy.
    Spowart G; Buckton KE; Skinner R; Emery AE
    Lancet; 1982 May; 1(8283):1251. PubMed ID: 6123008
    [No Abstract]   [Full Text] [Related]  

  • 18. Mental retardation locus in Xp21 chromosome microdeletion.
    Fries MH; Lebo RV; Schonberg SA; Golabi M; Seltzer WK; Gitelman SE; Golbus MS
    Am J Med Genet; 1993 Jun; 46(4):363-8. PubMed ID: 8357005
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular genetics of Duchenne muscular dystrophy.
    Tay J
    J Singapore Paediatr Soc; 1990; 32(3-4):61-4. PubMed ID: 2133759
    [No Abstract]   [Full Text] [Related]  

  • 20. [Trisomy 21 in a boy with progressive muscular dystrophy (Duchenne)].
    Moser H
    Z Kinderheilkd; 1971; 109(4):318-25. PubMed ID: 4252123
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.