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Journal Abstract Search

832 related items for PubMed ID: 10533026

  • 1. Filippi syndrome: report of three additional cases.
    Williams MS, Williams JL, Wargowski DS, Pauli RM, Pletcher BA.
    Am J Med Genet; 1999 Nov 19; 87(2):128-33. PubMed ID: 10533026
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  • 2. Craniodigital syndromes: report of a child with Filippi syndrome and discussion of differential diagnosis.
    Toriello HV, Higgins JV.
    Am J Med Genet; 1995 Jan 16; 55(2):200-4. PubMed ID: 7717418
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  • 3. The Dubowitz syndrome.
    Wilroy RS, Tipton RE, Summitt RL.
    Am J Med Genet; 1978 Jan 16; 2(3):275-84. PubMed ID: 263660
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  • 6. Mutchinick syndrome in a Japanese girl.
    Tonoki H, Hattori T, Kamoshida H, Ohta Y, Niikawa N.
    Am J Med Genet; 1999 Mar 12; 83(2):96-9. PubMed ID: 10190479
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  • 7. Lambotte syndrome: microcephaly, holoprosencephaly, intrauterine growth retardation, facial anomalies, and early lethality--a new sublethal multiple congenital anomaly/mental retardation syndrome in four sibs.
    Verloes A, Dodinval P, Beco L, Bonnivert J, Lambotte C.
    Am J Med Genet; 1990 Sep 12; 37(1):119-23. PubMed ID: 2240028
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  • 10. Short stature, microcephaly, characteristic face, syndactyly and mental retardation: the Filippi syndrome. Report on a second family.
    Meinecke P.
    Genet Couns; 1993 Sep 12; 4(2):147-51. PubMed ID: 8395190
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  • 12. Two female siblings with a previously unreported MCA/MR syndrome: pre- and postnatal growth retardation, iris colobomata, spasticity, facial dysmorphism and dilated ventricles.
    Yüksel A, Seven M, Deviren A, Söylemez MA, Hacihanefioğlu S, Ulutin T, Cenani A.
    Genet Couns; 1999 Sep 12; 10(3):265-9. PubMed ID: 10546098
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  • 13. Floating-Harbor syndrome in a Kuwaiti patient: a case report and literature review.
    Bastaki L, El-Nabi MM, Azab AS, Gouda SA, Al-Wadaani AM, Naguib KK.
    East Mediterr Health J; 2007 Sep 12; 13(4):975-9. PubMed ID: 17955782
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  • 14. Syndactyly type 1 with cataracts and mental retardation.
    Pavone L, Fiumara A, Rizzo R, Parano E, Incorpora G.
    Clin Dysmorphol; 1993 Jul 12; 2(3):257-9. PubMed ID: 8287189
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  • 17. Microcephaly and digital anomalies: a newly recognized syndrome of recessively inherited mental retardation.
    Kelly TE, Kirson L, Wyatt J.
    Am J Med Genet; 1993 Feb 01; 45(3):353-5. PubMed ID: 8434622
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  • 18. A 2q24.3q31.1 microdeletion found in a patient with Filippi-like syndrome phenotype: a case report.
    Lazier J, Chernos J, Lowry RB.
    Am J Med Genet A; 2014 Sep 01; 164A(9):2385-7. PubMed ID: 24924433
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  • 19. A new locus for Seckel syndrome on chromosome 18p11.31-q11.2.
    Børglum AD, Balslev T, Haagerup A, Birkebaek N, Binderup H, Kruse TA, Hertz JM.
    Eur J Hum Genet; 2001 Oct 01; 9(10):753-7. PubMed ID: 11781686
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  • 20. Unusual facial appearance, microcephaly, growth and mental retardation, and syndactyly. A new syndrome?
    Filippi G.
    Am J Med Genet; 1985 Dec 01; 22(4):821-4. PubMed ID: 4073130
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