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Journal Abstract Search

169 related items for PubMed ID: 1570839

  • 21. Gene localisation of X-linked hypohidrotic ectodermal dysplasia (C-S-T syndrome).
    MacDermot KD, Winter RM, Malcolm S.
    Hum Genet; 1986 Oct; 74(2):172-3. PubMed ID: 3464559
    [Abstract] [Full Text] [Related]

  • 22. X-linked mixed deafness with stapes fixation in a Mauritian kindred: linkage to Xq probe pDP34.
    Wallis C, Ballo R, Wallis G, Beighton P, Goldblatt J.
    Genomics; 1988 Nov; 3(4):299-301. PubMed ID: 3243543
    [Abstract] [Full Text] [Related]

  • 23. X-linked CHARGE-like Abruzzo-Erickson syndrome and classic cleft palate with ankyloglossia result from TBX22 splicing mutations.
    Pauws E, Peskett E, Boissin C, Hoshino A, Mengrelis K, Carta E, Abruzzo MA, Lees M, Moore GE, Erickson RP, Stanier P.
    Clin Genet; 2013 Apr; 83(4):352-8. PubMed ID: 22784330
    [Abstract] [Full Text] [Related]

  • 24. Linkage analysis in a large Brazilian family with van der Woude syndrome suggests the existence of a susceptibility locus for cleft palate at 17p11.2-11.1.
    Sertié AL, Sousa AV, Steman S, Pavanello RC, Passos-Bueno MR.
    Am J Hum Genet; 1999 Aug; 65(2):433-40. PubMed ID: 10417286
    [Abstract] [Full Text] [Related]

  • 25. X-linked cleft palate.
    Lowry RB.
    Birth Defects Orig Artic Ser; 1971 Jun; 7(7):76-9. PubMed ID: 5173246
    [Abstract] [Full Text] [Related]

  • 26. Multipoint linkage analysis in Menkes disease.
    Tønnesen T, Petterson A, Kruse TA, Gerdes AM, Horn N.
    Am J Hum Genet; 1992 May; 50(5):1012-7. PubMed ID: 1570830
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  • 29. Linkage in a family with X-linked Charcot-Marie-Tooth disease.
    Haites N, Fairweather N, Clark C, Kelly KF, Simpson S, Johnston AW.
    Clin Genet; 1989 Jun; 35(6):399-403. PubMed ID: 2567643
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  • 31. Mendelian inheritance of isolated nonsyndromic cleft palate.
    Rollnick BR, Kaye CI.
    Am J Med Genet; 1986 Jul; 24(3):465-73. PubMed ID: 3728565
    [Abstract] [Full Text] [Related]

  • 32. X linked spastic paraplegia (SPG2): clinical heterogeneity at a single gene locus.
    Bonneau D, Rozet JM, Bulteau C, Berthier M, Mettey R, Gil R, Munnich A, Le Merrer M.
    J Med Genet; 1993 May; 30(5):381-4. PubMed ID: 8320699
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  • 33. Nonsyndromic cleft lip and palate: no evidence of linkage to HLA or factor 13A.
    Hecht JT, Wang Y, Connor B, Blanton SH, Daiger SP.
    Am J Hum Genet; 1993 Jun; 52(6):1230-3. PubMed ID: 8099257
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  • 34. A new case of 2q duplication supports either a locus for orofacial clefting between markers D2S1897 and D2S2023 or a locus for cleft palate only on chromosome 2q13-q21.
    Ounap K, Ilus T, Laidre P, Uibo O, Tammur P, Bartsch O.
    Am J Med Genet A; 2005 Sep 01; 137A(3):323-7. PubMed ID: 16094674
    [Abstract] [Full Text] [Related]

  • 35. 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 01; 43(1):75-85. PubMed ID: 3163892
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  • 36. Anderson-Fabry disease--family linkage studies using two polymorphic X-linked DNA probes.
    Morgan SH, Cheshire JK, Wilson TM, MacDermot K, Crawfurd MA.
    Pediatr Nephrol; 1987 Jul 01; 1(3):536-9. PubMed ID: 2908672
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  • 39. Refinement of linkage of human severe combined immunodeficiency (SCIDX1) to polymorphic markers in Xq13.
    Puck JM, Conley ME, Bailey LC.
    Am J Hum Genet; 1993 Jul 01; 53(1):176-84. PubMed ID: 8317482
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  • 40. Cleft lip with cleft palate, ankyloglossia, and hypodontia are associated with TBX22 mutations.
    Kantaputra PN, Paramee M, Kaewkhampa A, Hoshino A, Lees M, McEntagart M, Masrour N, Moore GE, Pauws E, Stanier P.
    J Dent Res; 2011 Apr 01; 90(4):450-5. PubMed ID: 21248356
    [Abstract] [Full Text] [Related]

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