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 *

171 related articles for article (PubMed ID: 1979306)

  • 1. Assignment of the Nance-Horan syndrome to the distal short arm of the X chromosome.
    Zhu D; Alcorn DM; Antonarakis SE; Levin LS; Huang PC; Mitchell TN; Warren AC; Maumenee IH
    Hum Genet; 1990 Nov; 86(1):54-8. PubMed ID: 1979306
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Nance-Horan syndrome: linkage analysis in 4 families refines localization in Xp22.31-p22.13 region.
    Toutain A; Ronce N; Dessay B; Robb L; Francannet C; Le Merrer M; Briard ML; Kaplan J; Moraine C
    Hum Genet; 1997 Feb; 99(2):256-61. PubMed ID: 9048931
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mapping X-linked ophthalmic diseases. IV. Provisional assignment of the locus for X-linked congenital cataracts and microcornea (the Nance-Horan syndrome) to Xp22.2-p22.3.
    Lewis RA; Nussbaum RL; Stambolian D
    Ophthalmology; 1990 Jan; 97(1):110-20; discussion 120-1. PubMed ID: 1969135
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The Nance-Horan syndrome: a rare X-linked ocular-dental trait with expression in heterozygous females.
    Bixler D; Higgins M; Hartsfield J
    Clin Genet; 1984 Jul; 26(1):30-5. PubMed ID: 6467651
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Nance-Horan syndrome in females due to a balanced X;1 translocation that disrupts the NHS gene: Familial case report and review of the literature.
    Gómez-Laguna L; Martínez-Herrera A; Reyes-de la Rosa ADP; García-Delgado C; Nieto-Martínez K; Fernández-Ramírez F; Valderrama-Atayupanqui TY; Morales-Jiménez AB; Villa-Morales J; Kofman S; Cervantes A; Morán-Barroso VF
    Ophthalmic Genet; 2018; 39(1):56-62. PubMed ID: 28922055
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Nance-Horan syndrome: linkage analysis in a family from The Netherlands.
    Bergen AA; ten Brink J; Schuurman EJ; Bleeker-Wagemakers EM
    Genomics; 1994 May; 21(1):238-40. PubMed ID: 8088793
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mapping the gene for X-linked cataracts and microcornea with facial, dental, and skeletal features to Xp22: an appraisal of the Nance-Horan syndrome.
    Lewis RA
    Trans Am Ophthalmol Soc; 1989; 87():658-728. PubMed ID: 2576480
    [No Abstract]   [Full Text] [Related]  

  • 9. Nance-Horan syndrome: a contiguous gene syndrome involving deletion of the amelogenin gene? A case report and molecular analysis.
    Franco E; Hodgson S; Lench N; Roberts GJ
    Oral Dis; 1995 Mar; 1(1):8-11. PubMed ID: 7553384
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mental retardation in Nance-Horan syndrome: clinical and neuropsychological assessment in four families.
    Toutain A; Ayrault AD; Moraine C
    Am J Med Genet; 1997 Aug; 71(3):305-14. PubMed ID: 9268101
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Clinical and genetic characterization of three families with Nance-Horan syndrome caused by NHS gene mutations].
    Li L; Zheng GY; Song JX; Yue JF; Tan N
    Zhonghua Yan Ke Za Zhi; 2024 Sep; 60(9):757-765. PubMed ID: 39267554
    [No Abstract]   [Full Text] [Related]  

  • 12. A novel small deletion in the NHS gene associated with Nance-Horan syndrome.
    Li H; Yang L; Sun Z; Yuan Z; Wu S; Sui R
    Sci Rep; 2018 Feb; 8(1):2398. PubMed ID: 29402928
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Confirmation and refinement of the genetic localization of the Coffin-Lowry syndrome locus in Xp22.1-p22.2.
    Biancalana V; Briard ML; David A; Gilgenkrantz S; Kaplan J; Mathieu M; Piussan C; Poncin J; Schinzel A; Oudet C
    Am J Hum Genet; 1992 May; 50(5):981-7. PubMed ID: 1349200
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Exclusion of RAI2 as the causative gene for Nance-Horan syndrome.
    Walpole SM; Ronce N; Grayson C; Dessay B; Yates JR; Trump D; Toutain A
    Hum Genet; 1999 May; 104(5):410-1. PubMed ID: 10394933
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A Turkish family with Nance-Horan Syndrome due to a novel mutation.
    Tug E; Dilek NF; Javadiyan S; Burdon KP; Percin FE
    Gene; 2013 Aug; 525(1):141-5. PubMed ID: 23566852
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Phenotype-genotype correlation in potential female carriers of X-linked developmental cataract (Nance-Horan syndrome).
    Khan AO; Aldahmesh MA; Mohamed JY; Alkuraya FS
    Ophthalmic Genet; 2012 Jun; 33(2):89-95. PubMed ID: 22229851
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel Xp22.13 microdeletion in Nance-Horan syndrome.
    Accogli A; Traverso M; Madia F; Bellini T; Vari MS; Pinto F; Capra V
    Birth Defects Res; 2017 Jul; 109(11):866-868. PubMed ID: 28464487
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel NHS mutation causes Nance-Horan Syndrome in a Chinese family.
    Tian Q; Li Y; Kousar R; Guo H; Peng F; Zheng Y; Yang X; Long Z; Tian R; Xia K; Lin H; Pan Q
    BMC Med Genet; 2017 Jan; 18(1):2. PubMed ID: 28061824
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A locus for isolated cataract on human Xp.
    Francis PJ; Berry V; Hardcastle AJ; Maher ER; Moore AT; Bhattacharya SS
    J Med Genet; 2002 Feb; 39(2):105-9. PubMed ID: 11836358
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Truncating mutation in the NHS gene: phenotypic heterogeneity of Nance-Horan syndrome in an asian Indian family.
    Ramprasad VL; Thool A; Murugan S; Nancarrow D; Vyas P; Rao SK; Vidhya A; Ravishankar K; Kumaramanickavel G
    Invest Ophthalmol Vis Sci; 2005 Jan; 46(1):17-23. PubMed ID: 15623749
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.