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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

169 related items for PubMed ID: 1570839

  • 41. Regional localization of polymorphic DNA loci on the proximal long arm of the X chromosome using deletions associated with choroideremia.
    Schwartz M, Yang HM, Niebuhr E, Rosenberg T, Page DC.
    Hum Genet; 1988 Feb; 78(2):156-60. PubMed ID: 3422216
    [Abstract] [Full Text] [Related]

  • 42. Sex-linked inheritance of cleft palate.
    Rushton AR.
    Hum Genet; 1979 Apr 27; 48(2):179-81. PubMed ID: 457141
    [Abstract] [Full Text] [Related]

  • 43. Cleft lip and palate: no evidence of linkage to transforming growth factor alpha.
    Hecht JT, Wang YP, Blanton SH, Michels VV, Daiger SP.
    Am J Hum Genet; 1991 Sep 27; 49(3):682-6. PubMed ID: 1679292
    [Abstract] [Full Text] [Related]

  • 44. Close linkage of the locus for X chromosome-linked severe combined immunodeficiency to polymorphic DNA markers in Xq11-q13.
    de Saint Basile G, Arveiler B, Oberlé I, Malcolm S, Levinsky RJ, Lau YL, Hofker M, Debre M, Fischer A, Griscelli C.
    Proc Natl Acad Sci U S A; 1987 Nov 27; 84(21):7576-9. PubMed ID: 3478714
    [Abstract] [Full Text] [Related]

  • 45. Time for T.
    Murray JC.
    Nat Genet; 2001 Oct 27; 29(2):107-9. PubMed ID: 11586288
    [Abstract] [Full Text] [Related]

  • 46. Isolation and developmental expression analysis of Tbx22, the mouse homolog of the human X-linked cleft palate gene.
    Bush JO, Lan Y, Maltby KM, Jiang R.
    Dev Dyn; 2002 Nov 27; 225(3):322-6. PubMed ID: 12412015
    [Abstract] [Full Text] [Related]

  • 47. X-linked mental retardation associated with cleft lip/palate maps to Xp11.3-q21.3.
    Siderius LE, Hamel BC, van Bokhoven H, de Jager F, van den Helm B, Kremer H, Heineman-de Boer JA, Ropers HH, Mariman EC.
    Am J Med Genet; 1999 Jul 30; 85(3):216-20. PubMed ID: 10398231
    [Abstract] [Full Text] [Related]

  • 48. Mental retardation, congenital heart defect, cleft palate, short stature, and facial anomalies: a new X-linked multiple congenital anomalies/mental retardation syndrome: clinical description and molecular studies.
    Hamel BC, Mariman EC, van Beersum SE, Schoonbrood-Lenssen AM, Ropers HH.
    Am J Med Genet; 1994 Jul 15; 51(4):591-7. PubMed ID: 7943045
    [Abstract] [Full Text] [Related]

  • 49. X-linked mental retardation syndrome with short stature, small hands and feet, seizures, cleft palate, and glaucoma is linked to Xq28.
    Armfield K, Nelson R, Lubs HA, Häne B, Schroer RJ, Arena F, Schwartz CE, Stevenson RE.
    Am J Med Genet; 1999 Jul 30; 85(3):236-42. PubMed ID: 10398235
    [Abstract] [Full Text] [Related]

  • 50. A further X-linked isolated nonsyndromic cleft palate family with a nonexpressing obligate affected male.
    Hall BD.
    Am J Med Genet; 1987 Jan 30; 26(1):239-40. PubMed ID: 3812573
    [No Abstract] [Full Text] [Related]

  • 51. Dystonia-parkinsonism syndrome (XDP) locus: flanking markers in Xq12-q21.1.
    Kupke KG, Graeber MB, Müller U.
    Am J Hum Genet; 1992 Apr 30; 50(4):808-15. PubMed ID: 1550125
    [Abstract] [Full Text] [Related]

  • 52.
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    [No Abstract] [Full Text] [Related]

  • 53. Choroideremia: further evidence for assignment of the locus to Xq13-Xq21.
    Schwartz M, Rosenberg T, Niebuhr E, Lundsteen C, Sardemann H, Andersen O, Yang HM, Lamm LU.
    Hum Genet; 1986 Dec 30; 74(4):449-52. PubMed ID: 2878872
    [Abstract] [Full Text] [Related]

  • 54. Autosomal dominant nonsyndromic cleft lip and palate: significant evidence of linkage at 18q21.1.
    Beiraghi S, Nath SK, Gaines M, Mandhyan DD, Hutchings D, Ratnamala U, McElreavey K, Bartoloni L, Antonarakis GS, Antonarakis SE, Radhakrishna U.
    Am J Hum Genet; 2007 Jul 30; 81(1):180-8. PubMed ID: 17564975
    [Abstract] [Full Text] [Related]

  • 55. Anderson Fabry disease, a close linkage with highly polymorphic DNA markers DXS17, DXS87 and DXS88.
    MacDermot KD, Morgan SH, Cheshire JK, Wilson TM.
    Hum Genet; 1987 Nov 30; 77(3):263-6. PubMed ID: 2890570
    [Abstract] [Full Text] [Related]

  • 56. Nonsyndromic cleft lip with or without cleft palate: evidence of linkage to BCL3 in 17 multigenerational families.
    Stein J, Mulliken JB, Stal S, Gasser DL, Malcolm S, Winter R, Blanton SH, Amos C, Seemanova E, Hecht JT.
    Am J Hum Genet; 1995 Aug 30; 57(2):257-72. PubMed ID: 7668251
    [Abstract] [Full Text] [Related]

  • 57. Mapping of the gene for X-linked dominant Charcot-Marie-Tooth neuropathy.
    Ionasescu VV, Trofatter J, Haines JL, Ionasescu R, Searby C.
    Neurology; 1992 Apr 30; 42(4):903-8. PubMed ID: 1565250
    [Abstract] [Full Text] [Related]

  • 58. Allan-Herndon syndrome. II. Linkage to DNA markers in Xq21.
    Schwartz CE, Ulmer J, Brown A, Pancoast I, Goodman HO, Stevenson RE.
    Am J Hum Genet; 1990 Sep 30; 47(3):454-8. PubMed ID: 2393020
    [Abstract] [Full Text] [Related]

  • 59. Multipoint linkage analysis in X-linked Alport syndrome.
    Hertz JM, Kruse TA, Thomsen A, Spencer ES.
    Hum Genet; 1991 Dec 30; 88(2):157-61. PubMed ID: 1684562
    [Abstract] [Full Text] [Related]

  • 60. Classification of oral clefts by affection site and laterality: a genotype-phenotype correlation study.
    Farina A, Wyszynski DF, Pezzetti F, Scapoli L, Martinelli M, Carinci F, Carls F, Nardelli GB, Tognon M, Carinci P.
    Orthod Craniofac Res; 2002 Aug 30; 5(3):185-91. PubMed ID: 12194669
    [Abstract] [Full Text] [Related]

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