BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

130 related articles for article (PubMed ID: 2163973)

  • 21. DNA linkage analysis of X-linked retinoschisis.
    Dahl N; Goonewardena P; Chotai J; Anvret M; Pettersson U
    Hum Genet; 1988 Mar; 78(3):228-32. PubMed ID: 2894345
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Nance-Horan syndrome: localization within the region Xp21.1-Xp22.3 by linkage analysis.
    Stambolian D; Lewis RA; Buetow K; Bond A; Nussbaum R
    Am J Hum Genet; 1990 Jul; 47(1):13-9. PubMed ID: 1971992
    [TBL] [Abstract][Full Text] [Related]  

  • 23. New insights into X-linked hypophosphatemia.
    Grieff M
    Curr Opin Nephrol Hypertens; 1997 Jan; 6(1):15-9. PubMed ID: 9051349
    [TBL] [Abstract][Full Text] [Related]  

  • 24. X-linked hypophosphatemic rickets and the murine Hyp homologue.
    Hruska KA; Rifas L; Cheng SL; Gupta A; Halstead L; Avioli L
    Am J Physiol; 1995 Mar; 268(3 Pt 2):F357-62. PubMed ID: 7900834
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Hypophosphatemia: mouse model for human familial hypophosphatemic (vitamin D-resistant) rickets.
    Eicher EM; Southard JL; Scriver CR; Glorieux FH
    Proc Natl Acad Sci U S A; 1976 Dec; 73(12):4667-71. PubMed ID: 188049
    [TBL] [Abstract][Full Text] [Related]  

  • 26. New insights into the pathogenesis of inherited phosphate wasting disorders.
    Econs MJ
    Bone; 1999 Jul; 25(1):131-5. PubMed ID: 10423038
    [TBL] [Abstract][Full Text] [Related]  

  • 27. X-linked hypophosphatemia (familial or sex-linked vitamin-D-resistant rickets). X-linked hypophosphatemic (Hyp) mice.
    Meyer RA
    Am J Pathol; 1985 Feb; 118(2):340-2. PubMed ID: 2982272
    [No Abstract]   [Full Text] [Related]  

  • 28. A YAC contig spanning the hypophosphatemic rickets disease gene (HYP) candidate region.
    Francis F; Rowe PS; Econs MJ; See CG; Benham F; O'Riordan JL; Drezner MK; Hamvas RM; Lehrach H
    Genomics; 1994 May; 21(1):229-37. PubMed ID: 8088792
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Improved genetic mapping of X linked retinoschisis.
    George ND; Payne SJ; Bill RM; Barton DE; Moore AT; Yates JR
    J Med Genet; 1996 Nov; 33(11):919-22. PubMed ID: 8950671
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Linkage relationship of X-linked juvenile retinoschisis with Xp22.1-p22.3 probes.
    Sieving PA; Bingham EL; Roth MS; Young MR; Boehnke M; Kuo CY; Ginsburg D
    Am J Hum Genet; 1990 Oct; 47(4):616-21. PubMed ID: 1977307
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Pex gene deletions in Gy and Hyp mice provide mouse models for X-linked hypophosphatemia.
    Strom TM; Francis F; Lorenz B; Böddrich A; Econs MJ; Lehrach H; Meitinger T
    Hum Mol Genet; 1997 Feb; 6(2):165-71. PubMed ID: 9063736
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Audiometric evidence for two forms of X-linked hypophosphatemia in humans, apparent counterparts of Hyp and Gy mutations in mouse.
    Boneh A; Reade TM; Scriver CR; Rishikof E
    Am J Med Genet; 1987 Aug; 27(4):997-1003. PubMed ID: 3425609
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Association between X-linked hypophosphatemic rickets and Klinefelter's syndrome: effects on growth and body proportion.
    Baroncelli GI; Bertelloni S; Perri G; Saggese G
    Hum Genet; 1995 May; 95(5):581-5. PubMed ID: 7759083
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Genetic mapping of four DNA markers (DXS16, DXS43, DXS85, and DXS143) from the p22 region of the human X chromosome.
    Brown CJ; Mahtani MM; Willard HF
    Hum Genet; 1988 Nov; 80(3):296-8. PubMed ID: 3192218
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Multipoint linkage analysis of the short arm of the human X chromosome in families with X-linked muscular dystrophy.
    Wilcox DE; Affara NA; Yates JR; Ferguson-Smith MA; Pearson PL
    Hum Genet; 1985; 70(4):365-75. PubMed ID: 3860471
    [TBL] [Abstract][Full Text] [Related]  

  • 36. X-linked hypophosphatemic rickets without "rickets".
    Econs MJ; Feussner JR; Samsa GP; Effman EL; Vogler JB; Martinez S; Friedman NE; Quarles LD; Drezner MK
    Skeletal Radiol; 1991; 20(2):109-14. PubMed ID: 2020857
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A gene (PEX) with homologies to endopeptidases is mutated in patients with X-linked hypophosphatemic rickets. The HYP Consortium.
    Nat Genet; 1995 Oct; 11(2):130-6. PubMed ID: 7550339
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Phosphate transport in osteoblasts from normal and X-linked hypophosphatemic mice.
    Rifas L; Dawson LL; Halstead LR; Roberts M; Avioli LV
    Calcif Tissue Int; 1994 Jun; 54(6):505-10. PubMed ID: 8082056
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Mapping of the glycine receptor alpha 2-subunit gene and the GABAA alpha 3-subunit gene on the mouse X chromosome.
    Derry JM; Barnard PJ
    Genomics; 1991 Jul; 10(3):593-7. PubMed ID: 1679744
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Picture of the month. X-linked dominant hypophosphatemic rickets.
    Mimouni F; Mughal Z; Tsang RC; Feingold M
    Am J Dis Child; 1988 Feb; 142(2):191-2. PubMed ID: 2829621
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.