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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

253 related items for PubMed ID: 3785238

  • 21. Coffin-Siris syndrome: a case of an extremely low birthweight infant with severe kyphoscoliosis.
    Suzumura H, Sakurai K, Kano K, Ichimura T.
    Acta Paediatr Jpn; 1996 Oct; 38(5):537-40. PubMed ID: 8942018
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  • 22. MCA/MR syndrome in two female siblings: new entity or variant examples of Coffin-Lowry versus Atkin-Flaitz syndromes?
    Jans A, Ippel EF, Dijkstra PF, Bijlsma JB.
    Genet Couns; 1992 Oct; 3(3):139-43. PubMed ID: 1388932
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  • 23. Syndrome of developmental retardation, facial and skeletal anomalies, and hyperphosphatasia in two sisters: nosology and genetics of the Coffin-Siris syndrome.
    Rabe P, Haverkamp F, Emons D, Rosskamp R, Zerres K, Passarge E.
    Am J Med Genet; 1991 Dec 01; 41(3):350-4. PubMed ID: 1724113
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  • 25. Autosomal recessive mode of inheritance of a Coffin-Siris like syndrome.
    Bonioli E, Palmieri A, Bertola A, Bellini C.
    Genet Couns; 1995 Dec 01; 6(4):309-12. PubMed ID: 8775417
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  • 28. Anesthetic management in a child with Coffin-Siris syndrome.
    Silvani P, Camporesi A, Zoia E, Leoncino S, Salvo I.
    Paediatr Anaesth; 2004 Aug 01; 14(8):698-700. PubMed ID: 15283836
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  • 29. Hallux duplication, postaxial polydactyly, absence of the corpus callosum, severe mental retardation, and additional anomalies in two unrelated patients: a new syndrome.
    Schinzel A, Schmid W.
    Am J Med Genet; 1980 Aug 01; 6(3):241-9. PubMed ID: 7424976
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  • 33. 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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  • 34. Hand anomalies in Russell Silver syndrome.
    Lahiri A, Lester R.
    J Plast Reconstr Aesthet Surg; 2009 Apr 01; 62(4):462-5. PubMed ID: 18171637
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  • 35. Pure 9p duplication syndrome with aplasia of the middle phalanges of the fifth fingers.
    Sato A, Suzuki T, Ikeno M, Takeda J, Yamamoto Y, Shinohara M, Makino S, Takeda S, Shimizu T, Itakura A.
    Eur J Med Genet; 2020 Oct 01; 63(10):104005. PubMed ID: 32693209
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  • 36. Further delineation of Costello syndrome.
    Teebi AS, Shaabani IS.
    Am J Med Genet; 1993 Aug 15; 47(2):166-8. PubMed ID: 8213898
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  • 37. Pilodentoungulardysplasia with microcephaly: a new ectodermal dysplasia/malformation syndrome.
    Tajara EH, Pinheiro M, Freire-Maia N.
    Am J Med Genet; 1987 Jan 15; 26(1):153-6. PubMed ID: 3812555
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  • 38. Unusual facial appearance, microcephaly, growth and mental retardation, and syndactyly. A new syndrome?
    Filippi G.
    Am J Med Genet; 1985 Dec 15; 22(4):821-4. PubMed ID: 4073130
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  • 39. Fryns syndrome: another example of non-lethal outcome with severe mental handicap.
    Hanssen AM, Schrander-Stumpel CT, Thiry PA, Fryns JP.
    Genet Couns; 1992 Dec 15; 3(4):187-93. PubMed ID: 1472353
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  • 40. [Tonoki syndrome].
    Tonoki H.
    Ryoikibetsu Shokogun Shirizu; 2001 Dec 15; (34 Pt 2):734-5. PubMed ID: 11528994
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