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PUBMED FOR HANDHELDS

Journal Abstract Search


185 related items for PubMed ID: 958800

  • 61. [The tricho-rhino-phalangeal syndrome].
    Fontaine G, Maroteaux P, Farriaux JP, Richard J, Roelens B.
    Arch Fr Pediatr; 1970; 27(6):635-47. PubMed ID: 5433050
    [No Abstract] [Full Text] [Related]

  • 62. Marchesani syndrome.
    Amla I, Krishna GS, Mruthyunijaya GT.
    J Indian Med Assoc; 1972 Dec 16; 59(12):517-20. PubMed ID: 4658301
    [No Abstract] [Full Text] [Related]

  • 63.
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  • 64. [Tricho-rhino-phalangeal syndrome].
    Giedion A.
    Helv Paediatr Acta; 1966 Nov 16; 21(5):475-85. PubMed ID: 5991804
    [No Abstract] [Full Text] [Related]

  • 65. Tricho-rhino-phalangeal syndrome.
    Gorlin RJ, Cohen MM, Wolfson J.
    Am J Dis Child; 1969 Oct 16; 118(4):595-9. PubMed ID: 5820605
    [No Abstract] [Full Text] [Related]

  • 66. Tricho-rhino-phalangeal syndrome type II. The Langer-Giedion syndrome.
    Murachi S, Itoh H, Sugiura Y.
    Jinrui Idengaku Zasshi; 1979 Mar 16; 24(1):27-36. PubMed ID: 313467
    [No Abstract] [Full Text] [Related]

  • 67. [Associated malformations of the head and extremities].
    Tridon P.
    J Genet Hum; 1974 Dec 16; 22(4):365-80. PubMed ID: 4282383
    [No Abstract] [Full Text] [Related]

  • 68. [Tricho-rhino-falangeal dysplasia type I. Giedion's syndrome].
    Nordshus T, Hagelsteen H.
    Tidsskr Nor Laegeforen; 1980 Feb 10; 100(4):218-9. PubMed ID: 7376155
    [No Abstract] [Full Text] [Related]

  • 69.
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  • 70. [Combined immunologic deficiencies in 2 girls with incomplete hair-nose-finger syndrome].
    Bernatowska E, Ryzko J, Litewska D, Winkielman J.
    Pediatr Pol; 1983 Jun 10; 58(6):549-53. PubMed ID: 6646914
    [No Abstract] [Full Text] [Related]

  • 71. Langer-Giedion syndrome: type II tricho-rhino-phalangeal dysplasia.
    Stoltzfus E, Ladda RL, Lloyd-Still J.
    J Pediatr; 1977 Aug 10; 91(2):277-80. PubMed ID: 301559
    [No Abstract] [Full Text] [Related]

  • 72. Tricho-rhino-phalangeal syndrome without exostoses, wih an interstitial deletion of 8q23.
    Goldblatt J, Smart RD.
    Clin Genet; 1986 May 10; 29(5):434-8. PubMed ID: 3742850
    [Abstract] [Full Text] [Related]

  • 73. Three sibs with phalangeal anomalies, microcephaly, severe mental retardation, and neurological abnormalities.
    Woods CG, Crouchman M, Huson SM.
    J Med Genet; 1992 Jul 10; 29(7):500-2. PubMed ID: 1640433
    [Abstract] [Full Text] [Related]

  • 74.
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  • 75. Weill-Marchesani syndrome. Growth hormone, thyroid and chromosome studies.
    Götz M, Schenk E.
    Z Kinderheilkd; 1973 Dec 12; 116(1):43-9. PubMed ID: 4203835
    [No Abstract] [Full Text] [Related]

  • 76.
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  • 77. Robin sequence and oligodactyly in mother and son.
    Robinow M, Johnson GF, Apesos J.
    Am J Med Genet; 1986 Oct 12; 25(2):293-7. PubMed ID: 3777025
    [Abstract] [Full Text] [Related]

  • 78.
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  • 79.
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  • 80. A new ectrodactyly syndrome?
    Landy SJ, Donnai D.
    Clin Dysmorphol; 1993 Apr 12; 2(2):169-72. PubMed ID: 8281282
    [Abstract] [Full Text] [Related]


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