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 *

165 related articles for article (PubMed ID: 2894172)

  • 1. Localization of the gene for X-linked nephrogenic diabetes insipidus to Xq28.
    Kambouris M; Dlouhy SR; Trofatter JA; Conneally PM; Hodes ME
    Am J Med Genet; 1988 Jan; 29(1):239-46. PubMed ID: 2894172
    [TBL] [Abstract][Full Text] [Related]  

  • 2. X-linked nephrogenic diabetes insipidus: from the ship Hopewell to RFLP studies.
    Bichet DG; Hendy GN; Lonergan M; Arthus MF; Ligier S; Pausova Z; Kluge R; Zingg H; Saenger P; Oppenheimer E
    Am J Hum Genet; 1992 Nov; 51(5):1089-1102. PubMed ID: 1357965
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A gene for nonspecific X-linked mental retardation (MRX41) is located in the distal segment of Xq28.
    Hamel BC; Kremer H; Wesby-van Swaay E; van den Helm B; Smits AP; Oostra BA; Ropers HH; Mariman EC
    Am J Med Genet; 1996 Jul; 64(1):131-3. PubMed ID: 8826463
    [TBL] [Abstract][Full Text] [Related]  

  • 4. X-linked nonspecific mental retardation (MRX16) mapping to distal Xq28: linkage study and neuropsychological data in a large family.
    Gendrot C; Ronce N; Raynaud M; Ayrault AD; Dourlens J; Castelnau P; Muh JP; Chelly J; Moraine C
    Am J Med Genet; 1999 Apr; 83(5):411-8. PubMed ID: 10232754
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Linkage analyses in families with nephrogenic diabetes insipidus.
    Knoers NV; van der Heyden H; van Oost BA; Monnens L; Willems J; Ropers HH
    Prog Clin Biol Res; 1989; 305():149-55. PubMed ID: 2569742
    [No Abstract]   [Full Text] [Related]  

  • 6. Autosomal recessive inheritance of vasopressin-resistant diabetes insipidus.
    Langley JM; Balfe JW; Selander T; Ray PN; Clarke JT
    Am J Med Genet; 1991 Jan; 38(1):90-4. PubMed ID: 1672792
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Nephrogenic diabetes insipidus: close linkage with markers from the distal long arm of the human X chromosome.
    Knoers N; van der Heyden H; van Oost BA; Ropers HH; Monnens L; Willems J
    Hum Genet; 1988 Sep; 80(1):31-8. PubMed ID: 2843456
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Linkage of X-linked nephrogenic diabetes insipidus with DXS52, a polymorphic DNA marker.
    Knoers N; vd Heyden H; von Oost BA; Monnens L; Willems J; Ropers HH
    Nephron; 1988; 50(3):187-90. PubMed ID: 3226453
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Linkage analysis of bipolar illness with X-chromosome DNA markers: a susceptibility gene in Xq27-q28 cannot be excluded.
    De bruyn A; Raeymaekers P; Mendelbaum K; Sandkuijl LA; Raes G; Delvenne V; Hirsch D; Staner L; Mendlewicz J; Van Broeckhoven C
    Am J Med Genet; 1994 Dec; 54(4):411-9. PubMed ID: 7726217
    [TBL] [Abstract][Full Text] [Related]  

  • 10. X-linked myopia: Bornholm eye disease. Linkage to DNA markers on the distal part of Xq.
    Schwartz M; Haim M; Skarsholm D
    Clin Genet; 1990 Oct; 38(4):281-6. PubMed ID: 1980096
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Linkage and genetic counselling for the fragile X using DNA probes 52A, F9, DX13, and ST14.
    Mulley JC; Gedeon AK; Thorn KA; Bates LJ; Sutherland GR
    Am J Med Genet; 1987 Jun; 27(2):435-48. PubMed ID: 2886048
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Linkage localization of the thoraco-abdominal syndrome (TAS) gene to Xq25-26.
    Parvari R; Weinstein Y; Ehrlich S; Steinitz M; Carmi R
    Am J Med Genet; 1994 Feb; 49(4):431-4. PubMed ID: 7909197
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Linkage of X-linked myopathy with excessive autophagy (XMEA) to Xq28.
    Villard L; des Portes V; Levy N; Louboutin JP; Recan D; Coquet M; Chabrol B; Figarella-Branger D; Chelly J; Pellissier JF; Fontes M
    Eur J Hum Genet; 2000 Feb; 8(2):125-9. PubMed ID: 10757644
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Regional localization of two MRX genes to Xq28 (MRX28) and to Xp11.4-Xp22.12 (MRX33).
    Holinski-Feder E; Golla A; Rost I; Seidel H; Rittinger O; Meindl A
    Am J Med Genet; 1996 Jul; 64(1):125-30. PubMed ID: 8826462
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Three-point linkage analysis using multiple DNA polymorphic markers in families with X-linked nephrogenic diabetes insipidus.
    Knoers N; van der Heyden H; van Oost BA; Monnens L; Willems J; Ropers HH
    Genomics; 1989 Apr; 4(3):434-7. PubMed ID: 2714800
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. A gene for non-specific X-linked mental retardation (MRX55) is located in Xp11.
    Deqaqi SC; N'Guessan M; Forner J; Sbiti A; Beldjord C; Chelly J; Sefiani A; Des Portes V
    Ann Genet; 1998; 41(1):11-6. PubMed ID: 9599645
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Non-specific X-linked mental retardation: linkage analysis in MRX2 and MRX4 families revisited.
    Hu LJ; Blumenfeld-Heyberger S; Hanauer A; Weissenbach J; Mandel JL
    Am J Med Genet; 1994 Jul; 51(4):569-74. PubMed ID: 7943041
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mapping the gene causing X-linked recessive nephrolithiasis to Xp11.22 by linkage studies.
    Scheinman SJ; Pook MA; Wooding C; Pang JT; Frymoyer PA; Thakker RV
    J Clin Invest; 1993 Jun; 91(6):2351-7. PubMed ID: 8099916
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.