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Journal Abstract Search

123 related items for PubMed ID: 3316825

  • 1. The Dubowitz syndrome--one more case.
    Chrzanowska KH, Krajewska-Walasek M.
    Klin Padiatr; 1987; 199(5):370-2. PubMed ID: 3316825
    [Abstract] [Full Text] [Related]

  • 2. [Dubowitz syndrome. A diagnosis not to be missed].
    Mathieu M, Berquin P, Epelbaum S, Lenaerts C, Piussan C.
    Arch Fr Pediatr; 1991 Dec; 48(10):715-8. PubMed ID: 1793348
    [Abstract] [Full Text] [Related]

  • 3. The Dubowitz syndrome.
    Wilroy RS, Tipton RE, Summitt RL.
    Am J Med Genet; 1978 Dec; 2(3):275-84. PubMed ID: 263660
    [Abstract] [Full Text] [Related]

  • 4. 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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  • 5. Dubowitz syndrome: review of 141 cases including 36 previously unreported patients.
    Tsukahara M, Opitz JM.
    Am J Med Genet; 1996 May 03; 63(1):277-89. PubMed ID: 8723121
    [Abstract] [Full Text] [Related]

  • 6. Dubowitz syndrome: a cholesterol metabolism disorder?
    Yeşilkaya E, Karaer K, Bideci A, Camurdan O, Perçin EF, Cinaz P.
    Genet Couns; 2008 May 03; 19(3):287-90. PubMed ID: 18990984
    [Abstract] [Full Text] [Related]

  • 7. Sudden development of bilateral cataract in a child with Dubowitz syndrome: a case report.
    Annemans I, Foets B, Jaeken J, Casteels I.
    Bull Soc Belge Ophtalmol; 2000 May 03; (278):23-5. PubMed ID: 11761556
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  • 10. [Dubowitz syndrome: a dysmorphism syndrome with developmental delay, transitory short stature, hyperactive behavior and atopic dermatitis].
    Hochreutener H, Schinzel A, Baerlocher K.
    Monatsschr Kinderheilkd; 1990 Oct 03; 138(10):689-91. PubMed ID: 2079946
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  • 12. A previously undescribed autosomal recessive multiple congenital anomalies/mental retardation (MCA/MR) syndrome with growth failure, lip/palate cleft(s), and urogenital anomalies.
    Malpuech G, Demeocq F, Palcoux JB, Vanlieferinghen P.
    Am J Med Genet; 1983 Dec 03; 16(4):475-80. PubMed ID: 6660246
    [Abstract] [Full Text] [Related]

  • 13. Goldberg-Shprintzen syndrome: Hirschsprung disease, hypotonia, and ptosis in sibs.
    Yomo A, Taira T, Kondo I.
    Am J Med Genet; 1991 Nov 01; 41(2):188-91. PubMed ID: 1785632
    [Abstract] [Full Text] [Related]

  • 14. Familial transmission of a dysmorphic syndrome: a variant example of Kabuki syndrome?
    Belengeanu V, Rozsnyai K, Farcaş S, Velea I, Fryns JP.
    Genet Couns; 2005 Nov 01; 16(2):167-71. PubMed ID: 16080297
    [Abstract] [Full Text] [Related]

  • 15. A new syndrome of dwarfism, brachydactyly, nail dysplasia, and mental retardation in sibs.
    Tonoki H, Kishino T, Niikawa N.
    Am J Med Genet; 1990 May 01; 36(1):89-93. PubMed ID: 2333912
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  • 16. [Cardiac symptoms in 2 patients with Seckel syndrome].
    Rappen U, von Brenndorff AI.
    Monatsschr Kinderheilkd; 1993 Jul 01; 141(7):584-6. PubMed ID: 8413337
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  • 17. 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 01; 37(1):119-23. PubMed ID: 2240028
    [Abstract] [Full Text] [Related]

  • 18. Mental retardation, unusual face, and intrauterine growth retardation: a new recessive syndrome?
    Pitt DB, Rogers JG, Danks DM.
    Am J Med Genet; 1984 Oct 01; 19(2):307-13. PubMed ID: 6542309
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  • 19. A case of Seckel syndrome with Tetralogy of Fallot.
    Can E, Bulbul A, Uslu S, Demirin H, Comert S, Bolat F, Nuhoglu A.
    Genet Couns; 2010 Oct 01; 21(1):49-51. PubMed ID: 20420029
    [Abstract] [Full Text] [Related]

  • 20. Cleft palate-lateral synechiae syndrome: report on three new patients with additional findings and evidence for variability and heterogeneity.
    Nakata NM, Guion-Almeida ML, Richieri-Costa A.
    Am J Med Genet; 1993 Sep 01; 47(3):330-2. PubMed ID: 8135276
    [Abstract] [Full Text] [Related]

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