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: 1346773)

  • 21. Localization of the X-linked retinitis pigmentosa locus between DXS7 and DXS84 in a family showing tapetal reflex in heterozygotes.
    Chen JD; Halliday F; Serravalle S; Denton M
    Ophthalmic Paediatr Genet; 1988 Nov; 9(3):143-7. PubMed ID: 2906743
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Wiskott-Aldrich syndrome carrier detection with the hypervariable marker M27 beta.
    de Saint Basile G; Notarangelo LD; Bonaiti-Pellié C; Doussau M; Prolini O; Craig IW; Ugazio A; Griscelli C; Fischer A
    Hum Genet; 1992 May; 89(2):223-8. PubMed ID: 1350264
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Wiskott-Aldrich syndrome: new molecular and biochemical insights.
    Peacocke M; Siminovitch KA
    J Am Acad Dermatol; 1992 Oct; 27(4):507-19. PubMed ID: 1401301
    [TBL] [Abstract][Full Text] [Related]  

  • 24. The Wiskott-Aldrich syndrome.
    Peacocke M; Siminovitch KA
    Semin Dermatol; 1993 Sep; 12(3):247-54. PubMed ID: 8105860
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Aland eye disease: linkage data.
    Schwartz M; Rosenberg T
    Genomics; 1991 Jun; 10(2):327-32. PubMed ID: 2071141
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Carrier detection in Wiskott-Aldrich syndrome: combined use of M27 beta for X-inactivation studies and as a linked probe.
    Goodship J; Carter J; Espanol T; Boyd Y; Malcolm S; Levinsky RJ
    Blood; 1991 Jun; 77(12):2677-81. PubMed ID: 2043768
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Linkage relationships between X-linked retinitis pigmentosa and nine short-arm markers: exclusion of the disease locus from Xp21 and localization to between DXS7 and DXS14.
    Wright AF; Bhattacharya SS; Clayton JF; Dempster M; Tippett P; McKeown CM; Jay M; Jay B; Bird AC
    Am J Hum Genet; 1987 Oct; 41(4):635-44. PubMed ID: 3477957
    [TBL] [Abstract][Full Text] [Related]  

  • 28. X-linked hypohidrotic ectodermal dysplasia: localization within the region Xq11-21.1 by linkage analysis and implications for carrier detection and prenatal diagnosis.
    Zonana J; Clarke A; Sarfarazi M; Thomas NS; Roberts K; Marymee K; Harper PS
    Am J Hum Genet; 1988 Jul; 43(1):75-85. PubMed ID: 3163892
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Localization of X chromosome short arm markers relative to synovial sarcoma- and renal adenocarcinoma-associated translocation breakpoints.
    Sinke RJ; de Leeuw B; Janssen HA; Weghuis DO; Suijkerbuijk RF; Meloni AM; Gilgenkrantz S; Berger W; Ropers HH; Sandberg AA
    Hum Genet; 1993 Oct; 92(3):305-8. PubMed ID: 8406438
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A variant of Wiskott-Aldrich syndrome with nephropathy is linked to DXS255.
    Bennett CP; Barnicoat AJ; Cotter F; Wang Q; Mathew CG
    J Med Genet; 1995 Sep; 32(9):757-8. PubMed ID: 8544203
    [No Abstract]   [Full Text] [Related]  

  • 31. Mapping of locus for X-linked congenital stationary night blindness (CSNB1) proximal to DXS7.
    Bech-Hansen NT; Moore BJ; Pearce WG
    Genomics; 1992 Feb; 12(2):409-11. PubMed ID: 1740347
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Definitive localization of Becker muscular dystrophy in Xp by linkage to a cluster of DNA polymorphisms (DXS43 and DXS9).
    Fadda S; Mochi M; Roncuzzi L; Sangiorgi S; Sbarra D; Zatz M; Romeo G
    Hum Genet; 1985; 71(1):33-6. PubMed ID: 2993155
    [TBL] [Abstract][Full Text] [Related]  

  • 33. An 18-locus linkage map of the pericentromeric region of the human X chromosome: genetic framework for mapping X-linked disorders.
    Mahtani MM; Lafrenière RG; Kruse TA; Willard HF
    Genomics; 1991 Aug; 10(4):849-57. PubMed ID: 1916819
    [TBL] [Abstract][Full Text] [Related]  

  • 34. X-linked thrombocytopenia and Wiskott-Aldrich syndrome: similar regional assignment but distinct X-inactivation pattern in carriers.
    De Saint-Basile G; Schlegel N; Caniglia M; Le Deist F; Kaplan C; Lecompte T; Piller F; Fischer A; Griscelli C
    Ann Hematol; 1991 Aug; 63(2):107-10. PubMed ID: 1912030
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Localization of the microsatellite probe DXS426 between DXS7 and DXS255 on Xp and linkage to X-linked retinitis pigmentosa.
    Coleman M; Bhattacharya S; Lindsay S; Wright A; Jay M; Litt M; Craig I; Davies K
    Am J Hum Genet; 1990 Dec; 47(6):935-40. PubMed ID: 2239970
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Application of molecular analysis to genetic counseling in the Wiskott-Aldrich syndrome (WAS).
    Notarangelo LD; Candotti F; Parolini O; Mantuano E; Giliani S; Lanfranchi A; Albertini A
    DNA Cell Biol; 1993 Sep; 12(7):645-9. PubMed ID: 8397823
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Close linkage between Norrie disease, a cloned DNA sequence from the proximal short arm, and the centromere of the X chromosome.
    Bleeker-Wagemakers LM; Friedrich U; Gal A; Wienker TF; Warburg M; Ropers HH
    Hum Genet; 1985; 71(3):211-4. PubMed ID: 2998969
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. Gene localization in a family with X-linked syndromal mental retardation (Prieto syndrome).
    Watty A; Prieto F; Beneyto M; Neugebauer M; Gal A
    Am J Med Genet; 1991; 38(2-3):234-9. PubMed ID: 1673297
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Identification of a highly polymorphic marker within intron 7 of the ALAS2 gene and suggestion of at least two loci for X-linked sideroblastic anemia.
    Cox TC; Kozman HM; Raskind WH; May BK; Mulley JC
    Hum Mol Genet; 1992 Nov; 1(8):639-41. PubMed ID: 1301172
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.