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Journal Abstract Search

148 related items for PubMed ID: 7166592

  • 1.
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  • 3. A familial syndrome with hypotonia, mental retardation and dysmorphic features resembling Cohen syndrome.
    Mejía-Baltodano G, Bobadilla L, Solís A, Mendoza R, Díaz-Gallardo MY, Barros-Núñez P.
    Genet Couns; 1997; 8(4):311-6. PubMed ID: 9457500
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  • 4. [Cohen syndrome in 2 brothers].
    Zetler S, Römke C, Aksu F.
    Klin Padiatr; 1987; 199(1):55-7. PubMed ID: 3560767
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  • 7. The Cohen syndrome: report of a case.
    Naritomi K, Chinen Y.
    Jpn J Hum Genet; 1997 Sep; 42(3):457-9. PubMed ID: 12503195
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  • 8. [Cohen syndrome. A new case and review of the literature].
    Calzolari S, Ballardini M, De Marco P.
    Minerva Pediatr; 1995 Mar; 47(3):83-7. PubMed ID: 7791717
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  • 9. Confirmation of the Cohen syndrome.
    Carey JC, Hall BD.
    J Pediatr; 1978 Aug; 93(2):239-44. PubMed ID: 671157
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  • 10. [Cohen syndrome].
    Kayashima T, Niikawa N.
    Ryoikibetsu Shokogun Shirizu; 2001 Aug; (36):477-8. PubMed ID: 11596442
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  • 14. MORM syndrome (mental retardation, truncal obesity, retinal dystrophy and micropenis), a new autosomal recessive disorder, links to 9q34.
    Hampshire DJ, Ayub M, Springell K, Roberts E, Jafri H, Rashid Y, Bond J, Riley JH, Woods CG.
    Eur J Hum Genet; 2006 May; 14(5):543-8. PubMed ID: 16493448
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  • 15. Identical twins with Cohen syndrome.
    North KN, Fulton AB, Whiteman DA.
    Am J Med Genet; 1995 Jul 31; 58(1):54-8. PubMed ID: 7573157
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  • 16. [Cohen syndrome. Personal case report and literature review].
    Oztürk B, Weber HP.
    Monatsschr Kinderheilkd; 1991 Dec 31; 139(12):844-8. PubMed ID: 1770962
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  • 17. Mental retardation, obesity, mandibular prognathism with eye and skin anomalies (MOMES syndrome): a newly recognized autosomal recessive syndrome.
    Kantaputra PN, Kunachaichote J, Patikulsila P.
    Am J Med Genet; 2001 Nov 01; 103(4):283-8. PubMed ID: 11746007
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  • 18. [Cohen syndrome, an autosomal recessive disease? (author's transl)].
    Ferré P, Fournet JP, Courpotin C.
    Arch Fr Pediatr; 1982 Mar 01; 39(3):159-60. PubMed ID: 7103672
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  • 19. [Joubert's syndrome: report of 12 cases].
    Barreirinho MS, Teixeira J, Moreira NC, Bastos S, Gonçalvez S, Barbot MC.
    Rev Neurol; 1982 Mar 01; 32(9):812-7. PubMed ID: 11424029
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  • 20. FG syndrome: the trias mental retardation, hypotonia and constipation reviewed.
    Zwamborn-Hanssen AM, Schrander-Stumpel CT, Smeets E, Decock P, Fryns JP.
    Genet Couns; 1995 Mar 01; 6(4):313-9. PubMed ID: 8775418
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