These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

112 related articles for article (PubMed ID: 7774942)

  • 21. The Marfan syndrome locus: confirmation of assignment to chromosome 15 and identification of tightly linked markers at 15q15-q21.3.
    Dietz HC; Pyeritz RE; Hall BD; Cadle RG; Hamosh A; Schwartz J; Meyers DA; Francomano CA
    Genomics; 1991 Feb; 9(2):355-61. PubMed ID: 2004786
    [TBL] [Abstract][Full Text] [Related]  

  • 22. The genetic linkage between the PKU locus and the loci for amylase 1, amylase 2, Fy, PGM 1, and Rh and the question of assignment of the PKU locus to chromosome no. 1.
    Knapp A; Tintschewa R; Scheibe E; Scheibe E; Jäger B; Biebler KE
    Hum Genet; 1982; 60(2):122-5. PubMed ID: 6176531
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Linkage relationships of the gene for apolipoprotein CII with loci on chromosome 19.
    Donald JA; Wallis SC; Kessling A; Tippett P; Robson EB; Ball S; Davies KE; Scambler P; Berg K; Heiberg A
    Hum Genet; 1985; 69(1):39-43. PubMed ID: 3855405
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Genetic heterogeneity of early-onset familial breast cancer.
    Sobol H; Mazoyer S; Narod SA; Smith SA; Black DM; Kerbrat P; Jamot B; Solomon E; Ponder BA; Guerin D
    Hum Genet; 1992 Jun; 89(4):381-3. PubMed ID: 1352270
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A rare PvuII RFLP at the CRYB1 locus (17q11.2----17q12).
    Barker DF; Fain PR; Wright EC; Nguyen K; Tsui LC
    Nucleic Acids Res; 1989 Jan; 17(2):826. PubMed ID: 2563585
    [No Abstract]   [Full Text] [Related]  

  • 26. MspI RFLP at CRYB1 locus (17q11.2----17q12).
    Barker DF; Fain PR; Wright EC; Nguyen K; Tsui LC
    Nucleic Acids Res; 1989 Jan; 17(2):827. PubMed ID: 2464799
    [No Abstract]   [Full Text] [Related]  

  • 27. A polymorphic DNA marker on chromosome 10 linked to RBP3 on the MEN2A side.
    Wu J; Cavenee WK; Miki T; Kidd KK
    Cytogenet Cell Genet; 1988; 48(4):246-7. PubMed ID: 2907872
    [No Abstract]   [Full Text] [Related]  

  • 28. A moderately frequent HindIII polymorphism at the human NGFR locus (17q12----17q22).
    Wright EC; Fain PR; Barker DF; Chao MV
    Nucleic Acids Res; 1989 Jan; 17(2):825. PubMed ID: 2563584
    [No Abstract]   [Full Text] [Related]  

  • 29. Localization of the nucleotide excision repair gene ERCC6 to human chromosome 10q11-q21.
    Troelstra C; Landsvater RM; Wiegant J; van der Ploeg M; Viel G; Buys CH; Hoeijmakers JH
    Genomics; 1992 Apr; 12(4):745-9. PubMed ID: 1349298
    [TBL] [Abstract][Full Text] [Related]  

  • 30. X-linked agammaglobulinemia and the red blood cell determinants Xg and 12E7 are not closely linked.
    Mensink EJ; Schot JD; Tippett P; Ott J; Schuurman RK
    Hum Genet; 1984; 68(4):303-9. PubMed ID: 6595200
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Autosomal dominant aniridia linked to the chromosome 11p13 markers catalase and D11S151 in a large Dutch family.
    Mannens M; Bleeker-Wagemakers EM; Bliek J; Hoovers J; Mandjes I; van Tol S; Frants RR; Heyting C; Westerveld A; Slater RM
    Cytogenet Cell Genet; 1989; 52(1-2):32-6. PubMed ID: 2575483
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Confirmation of the location of a Waardenburg syndrome type I mutation on human chromosome 2q. Tight linkage to FN1 and ALPP.
    Asher JH; Morell R; Friedman TB
    Ann N Y Acad Sci; 1991; 630():295-7. PubMed ID: 1683205
    [No Abstract]   [Full Text] [Related]  

  • 33. Absence of linkage of Noonan syndrome to the neurofibromatosis type 1 locus.
    Sharland M; Taylor R; Patton MA; Jeffery S
    J Med Genet; 1992 Mar; 29(3):188-90. PubMed ID: 1348095
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Chromosomal mapping of the blood group genes.
    Tippett P
    Semin Hematol; 1981 Jan; 18(1):4-12. PubMed ID: 6782679
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Human amylase loci: genetic linkage with the Duffy blood group locus and assignment to linkage group I.
    Merritt AD; Lovrien EW; Rivas ML; Conneally PM
    Am J Hum Genet; 1973 Sep; 25(5):523-38. PubMed ID: 4741847
    [No Abstract]   [Full Text] [Related]  

  • 36. Chromosome 21 genetic linkage data set based on the Venezuelan reference pedigree.
    Haines JL; Trofatter JA; Tanzi RE; Watkins P; Wexler NS; Conneally PM; Gusella JF
    Cytogenet Cell Genet; 1992; 59(2-3):88-9. PubMed ID: 1346592
    [No Abstract]   [Full Text] [Related]  

  • 37. Two polymorphic TaqI sites at the human NGFR locus (17q12----17q22).
    Wright EC; Fain PR; Barker DF; Chao MV
    Nucleic Acids Res; 1989 Jan; 17(2):824. PubMed ID: 2563583
    [No Abstract]   [Full Text] [Related]  

  • 38. Linkage of autosomal dominant type I hereditary motor and sensory neuropathy to the Duffy locus on chromosome 1.
    Guiloff RJ; Thomas PK; Contreras M; Armitage S; Schwarz G; Sedgwick EM
    J Neurol Neurosurg Psychiatry; 1982 Aug; 45(8):669-74. PubMed ID: 7130990
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Improved definition of carrier status in X-linked hypohidrotic ectodermal dysplasia by use of restriction fragment length polymorphism-based linkage analysis.
    Zonana J; Sarfarazi M; Thomas NS; Clarke A; Marymee K; Harper PS
    J Pediatr; 1989 Mar; 114(3):392-9. PubMed ID: 2564048
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A new human RFLP identified by 7D2 places D13S10 proximal to esterase D.
    Bowcock AM; Farrer LA; Hebert JM; Bonne-Tamir B; Frydman M; Kidd KK; Cavalli-Sforza LL
    Cytogenet Cell Genet; 1987; 44(4):236-7. PubMed ID: 2884079
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.