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Journal Abstract Search

152 related items for PubMed ID: 7447519

  • 21. The Perlman syndrome: clinical and biological aspects.
    Neri G, Martini-Neri ME, Opitz JM, Freed JJ.
    Prog Clin Biol Res; 1985; 200():269-76. PubMed ID: 3001776
    [No Abstract] [Full Text] [Related]

  • 22. Short stature, abnormal face, joint laxity, dislocation, hernias, delayed bone age, and severe psychomotor retardation in two brothers: previously undescribed MCA/MR syndrome.
    Mégarbané A, Ruchoux MM, Loeys B, Ayoub N, Nuytinck L.
    Am J Med Genet; 2001 Dec 01; 104(3):221-4. PubMed ID: 11754048
    [Abstract] [Full Text] [Related]

  • 23. [Simpson-Golabi-Behmel syndrome. A new overgrowth syndrome with increased risk of tumor development].
    Weidle B, Orstavik KH.
    Tidsskr Nor Laegeforen; 1998 Apr 20; 118(10):1556-8. PubMed ID: 9615582
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  • 24. [Aarskog syndrome (author's transl)].
    Kunze J, Spranger J.
    Klin Padiatr; 1973 Nov 20; 185(6):490-4. PubMed ID: 4798676
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  • 26. Further delineation of the Simpson-Golabi-Behmel (SGB) syndrome.
    Lin AE.
    Am J Med Genet; 1993 Jun 15; 46(5):606-7. PubMed ID: 8322829
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  • 29. Hypertrichosis, pigmentary retinopathy, and facial anomalies: a new syndrome?
    Pivnick EK, Wilroy RS, Martens PR, Teather TC, Hashimoto K.
    Am J Med Genet; 1996 Apr 24; 62(4):386-90. PubMed ID: 8723069
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  • 30. CHARGE association.
    Toriello HV.
    Ear Nose Throat J; 1999 Jun 24; 78(6):413. PubMed ID: 10388189
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  • 38. [A casuistic contribution to potter syndrome of dysplasia renofacialis with and without sirenomelia (author's transl)].
    Kühner U, Buchinger G, Fricke G, Romen H.
    Klin Padiatr; 1976 May 24; 188(3):289-94. PubMed ID: 945426
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  • 39. Roberts syndrome: study of 4 new Rgyptian cases with comparison of clinical and cytogenetic findings.
    Temtamy SA, Ismail S, Helmy NA.
    Genet Couns; 2006 May 24; 17(1):1-13. PubMed ID: 16719272
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  • 40. Fallot complex, severe mental, and growth retardation: a new autosomal recessive syndrome?
    Bindewald B, Ulmer H, Müller U.
    Am J Med Genet; 1994 Apr 01; 50(2):173-6. PubMed ID: 8010348
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