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 *

121 related articles for article (PubMed ID: 7601447)

  • 1. High-density physical mapping of a 3-Mb region in Xp22.3 and refined localization of the gene for X-linked recessive chondrodysplasia punctata (CDPX1).
    Wang I; Franco B; Ferrero GB; Chinault AC; Weissenbach J; Chumakov I; Le Paslier D; Levilliers J; Klink A; Rappold GA; Ballabio A; Petit C
    Genomics; 1995 Mar; 26(2):229-38. PubMed ID: 7601447
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Refinement of the locus for X-linked recessive chondrodysplasia punctata.
    Muroya K; Ogata T; Rappold G; Klink A; Nakahori Y; Fukushima Y; Aizu K; Matsuo N
    Hum Genet; 1995 May; 95(5):577-80. PubMed ID: 7759082
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Absent chondrodysplasia punctata in a male with an Xp terminal deletion involving the putative region for CDPX1 locus.
    Ogata T; Goodfellow P; Petit C; Maroteaux P; Matsuo N
    Am J Med Genet; 1993 Jan; 45(1):101-4. PubMed ID: 8418639
    [TBL] [Abstract][Full Text] [Related]  

  • 4. An interstitial deletion in Xp22.3 in a family with X-linked recessive chondrodysplasia punctata and short stature.
    Petit C; Melki J; Levilliers J; Serville F; Weissenbach J; Maroteaux P
    Hum Genet; 1990 Jul; 85(2):247-50. PubMed ID: 2370057
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A 45,X male with an X;Y translocation: implications for the mapping of the genes responsible for Turner syndrome and X-linked chondrodysplasia punctata.
    Weil D; Portnoï MF; Levilliers J; Wang I; Mathieu M; Taillemite JL; Meier M; Boudailliez B; Petit C
    Hum Mol Genet; 1993 Nov; 2(11):1853-6. PubMed ID: 8281147
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A patient with an interstitial deletion in Xp22.3 locates the gene for X-linked recessive chondrodysplasia punctata to within a one megabase interval.
    Klink A; Meindl A; Hellebrand H; Rappold GA
    Hum Genet; 1994 Apr; 93(4):463-6. PubMed ID: 8168818
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Development and physical analysis of YAC contigs covering 7 Mb of Xp22.3-p22.2.
    Herrell S; Novo FJ; Charlton R; Affara NA
    Genomics; 1995 Jan; 25(2):526-37. PubMed ID: 7789987
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A cluster of sulfatase genes on Xp22.3: mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathy.
    Franco B; Meroni G; Parenti G; Levilliers J; Bernard L; Gebbia M; Cox L; Maroteaux P; Sheffield L; Rappold GA; Andria G; Petit C; Ballabio A
    Cell; 1995 Apr; 81(1):15-25. PubMed ID: 7720070
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The human protein kinase gene PKX1 on Xp22.3 displays Xp/Yp homology and is a site of chromosomal instability.
    Klink A; Schiebel K; Winkelmann M; Rao E; Horsthemke B; Lüdecke HJ; Claussen U; Scherer G; Rappold G
    Hum Mol Genet; 1995 May; 4(5):869-78. PubMed ID: 7633447
    [TBL] [Abstract][Full Text] [Related]  

  • 10. X-linked recessive chondrodysplasia punctata with XY translocation in a stillborn fetus.
    Van Maldergem L; Espeel M; Roels F; Petit C; Dacremont G; Wanders RJ; Verloes A; Gillerot Y
    Hum Genet; 1991 Oct; 87(6):661-4. PubMed ID: 1937466
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Characterization of a YAC contig spanning the pseudoautosomal region.
    Ried K; Mertz A; Nagaraja R; Trusgnich M; Riley JH; Anand R; Lehrach H; Page D; Ellison JW; Rappold G
    Genomics; 1995 Oct; 29(3):787-92. PubMed ID: 8575778
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Construction of a YAC contig and an STS map spanning 3.6 megabase pairs in Xp22.1.
    Trump D; Pilia G; Dixon PH; Wooding C; Thakrar R; Leigh SE; Nagaraja R; Whyte MP; Schlessinger D; Thakker RV
    Hum Genet; 1996 Jan; 97(1):60-8. PubMed ID: 8557262
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Long-range restriction map of the terminal part of the short arm of the human X chromosome.
    Petit C; Levilliers J; Weissenbach J
    Proc Natl Acad Sci U S A; 1990 May; 87(10):3680-4. PubMed ID: 2339111
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 2.6 Mb YAC contig of the human X inactivation center region in Xq13: physical linkage of the RPS4X, PHKA1, XIST and DXS128E genes.
    Lafrenière RG; Brown CJ; Rider S; Chelly J; Taillon-Miller P; Chinault AC; Monaco AP; Willard HF
    Hum Mol Genet; 1993 Aug; 2(8):1105-15. PubMed ID: 8401491
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Regional assignment of Y-linked DNA probes by deletion mapping and their homology with X-chromosome and autosomal sequences.
    Affara NA; Florentin L; Morrison N; Kwok K; Mitchell M; Cook A; Jamieson D; Glasgow L; Meredith L; Boyd E
    Nucleic Acids Res; 1986 Jul; 14(13):5353-73. PubMed ID: 3737403
    [TBL] [Abstract][Full Text] [Related]  

  • 16. X-linked recessive chondrodysplasia punctata due to a new point mutation of the ARSE gene.
    Parenti G; Buttitta P; Meroni G; Franco B; Bernard L; Rizzolo MG; Brunetti-Pierri N; Ballabio A; Andria G
    Am J Med Genet; 1997 Dec; 73(2):139-43. PubMed ID: 9409863
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Isolation of sequences from Xp22.3 and deletion mapping using sex chromosome rearrangements from human X-Y interchange sex reversals.
    Petit C; Levilliers J; Rouyer F; Simmler MC; Herouin E; Weissenbach J
    Genomics; 1990 Apr; 6(4):651-8. PubMed ID: 2341154
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosome.
    Ballabio A; Bardoni B; Carrozzo R; Andria G; Bick D; Campbell L; Hamel B; Ferguson-Smith MA; Gimelli G; Fraccaro M
    Proc Natl Acad Sci U S A; 1989 Dec; 86(24):10001-5. PubMed ID: 2602357
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Refined mapping and YAC contig construction of the X-linked cleft palate and ankyloglossia locus (CPX) including the proximal X-Y homology breakpoint within Xq21.3.
    Forbes SA; Brennan L; Richardson M; Coffey A; Cole CG; Gregory SG; Bentley DR; Mumm S; Moore GE; Stanier P
    Genomics; 1996 Jan; 31(1):36-43. PubMed ID: 8808277
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Brachytelephalangic dwarfism due to the loss of ARSE and SHOX genes resulting from an X;Y translocation.
    Seidel J; Schiller S; Kelbova C; Beensen V; Orth U; Vogt S; Claussen U; Zintl F; Rappold GA
    Clin Genet; 2001 Feb; 59(2):115-21. PubMed ID: 11260213
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.