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Journal Abstract Search

292 related items for PubMed ID: 7888143

  • 1. The facio-digito-genital syndrome (Aarskog syndrome): a further delineation of the distinct radiological findings.
    Lizcano-Gil LA, Garcia-Cruz D, Cantu JM, Fryns JP.
    Genet Couns; 1994; 5(4):387-92. PubMed ID: 7888143
    [Abstract] [Full Text] [Related]

  • 2. Short rib-polydactyly syndrome, Majewski type.
    Chen H, Yang SS, Gonzalez E, Fowler M, Al Saadi A.
    Am J Med Genet; 1980; 7(2):215-22. PubMed ID: 7468649
    [Abstract] [Full Text] [Related]

  • 3. Mild optic nerve hypoplasia with retinal venous tortuosity in aarskog (facial-digital-genital) syndrome.
    Jogiya A, Sandy C.
    Ophthalmic Genet; 2005 Sep; 26(3):139-41. PubMed ID: 16272060
    [Abstract] [Full Text] [Related]

  • 4. Multiple congenital anomalies associated with an oto-palato-digital syndrome type II.
    Blanchet P, Lefort G, Eglin MC, Rieu D, Sarda P.
    Genet Couns; 1993 Sep; 4(4):289-94. PubMed ID: 8110417
    [Abstract] [Full Text] [Related]

  • 5. Aarskog syndrome in a Brazilian boy born to consanguineous parents.
    Guion-Almeida ML, Richieri-Costa A.
    Am J Med Genet; 1992 Jul 15; 43(5):808-10. PubMed ID: 1642267
    [Abstract] [Full Text] [Related]

  • 6. [Genetic morphological fatal syndrome. Smith-Lemli-Opitz syndrome].
    Henkel KE, Pfeiffer RA, Stöss H.
    Pathologe; 1993 Mar 15; 14(2):91-2. PubMed ID: 8469651
    [No Abstract] [Full Text] [Related]

  • 7. The Aarskog (facio-digito-genital) syndrome.
    Hoo JJ.
    Clin Genet; 1979 Oct 15; 16(4):269-76. PubMed ID: 519896
    [Abstract] [Full Text] [Related]

  • 8. [Pyknodysostosis].
    Magnani F, Coppolino F, Loreto C, Greco S.
    Radiol Med; 1985 May 15; 71(5):351-3. PubMed ID: 4059604
    [No Abstract] [Full Text] [Related]

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  • 14. The Robinow syndrome: an isolated case with a detailed study of the phenotype.
    Kelly TE, Benson R, Temtamy S, Plotnick L, Levin S.
    Am J Dis Child; 1975 Mar 15; 129(3):383-6. PubMed ID: 1121970
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  • 15. The Aarskog syndrome in three brothers.
    Funderburk SJ, Crandall BF.
    Clin Genet; 1974 Mar 15; 6(2):119-24. PubMed ID: 4430151
    [No Abstract] [Full Text] [Related]

  • 16. Coffin-Lowry syndrome: clinical aspects at different ages and symptoms in female carriers.
    Plomp AS, De Die-Smulders CE, Meinecke P, Ypma-Verhulst JM, Lissone DA, Fryns JP.
    Genet Couns; 1995 Mar 15; 6(3):259-68. PubMed ID: 8588856
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  • 18. Otopalatodigital syndrome type II.
    Holder SE, Winter RM.
    J Med Genet; 1993 Apr 15; 30(4):310-3. PubMed ID: 8487277
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  • 20. [A new sublethal syndrome with multiple malformations associating diaphragmatic hernia, distal digital hypoplasia, and craniofacial anomalies. The "Fryns syndrome"].
    Fryns JP, Moerman P, Van den Berghe H, Aymé S.
    J Genet Hum; 1989 Sep 15; 37(3):203-5. PubMed ID: 2625623
    [Abstract] [Full Text] [Related]

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