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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

161 related items for PubMed ID: 1218209

  • 21. [Cranio-carpo-tarsal dysplasia].
    Nuñez E, Stuardo MC.
    Rev Chil Pediatr; 1971; 42(9):611-5. PubMed ID: 5150692
    [No Abstract] [Full Text] [Related]

  • 22. [Freeman-Sheldon syndrome in a 7-month-old infant].
    Ostrowski A, Dubiel A, Pietrzyk J.
    Przegl Lek; 1971; 28(7):506-8. PubMed ID: 5093035
    [No Abstract] [Full Text] [Related]

  • 23. The Greig cephalopolysyndactyly syndrome: report of a family and review of the literature.
    Gollop TR, Fontes LR.
    Am J Med Genet; 1985 Sep; 22(1):59-68. PubMed ID: 3901752
    [Abstract] [Full Text] [Related]

  • 24. [Coffin-Lowry syndrome. Description of a clinical case].
    Venura A, Ferrari P, Benci E, Grando A.
    Pediatr Med Chir; 1988 Sep; 10(4):449-50. PubMed ID: 3231552
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  • 28. [The cranio-carpo-tarsal dysplasia syndrome in a 6-year-old girl (whistling-face syndrome)].
    Zizka J, Lichý J, Balícek P.
    Cesk Pediatr; 1979 Feb; 34(2):96-7. PubMed ID: 106974
    [No Abstract] [Full Text] [Related]

  • 29. M--craniocarpotarsal dystrophy (whistling face syndrome) in two families.
    Jorgenson RJ.
    Birth Defects Orig Artic Ser; 1974 Feb; 10(5):237-42. PubMed ID: 4220006
    [No Abstract] [Full Text] [Related]

  • 30. Hyperphalangism, facial anomalies, hallux valgus, and bronchomalacia: a new syndrome?
    Chitayat D, Haj-Chahine S, Stalker HJ, Azouz EM, Côté A, Halal F.
    Am J Med Genet; 1993 Jan 01; 45(1):1-4. PubMed ID: 8418638
    [Abstract] [Full Text] [Related]

  • 31. Megalocornea associated with multiple skeletal anomalies: a new genetic syndrome?
    Frank Y, Ziprkowski M, Romano A, Stein R, Katznelson MB, Cohen B, Goodman RM.
    J Genet Hum; 1973 Jun 01; 21(2):67-72. PubMed ID: 4805907
    [No Abstract] [Full Text] [Related]

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  • 33. Previously undescribed syndrome of craniofacial, hand anomalies, and sensorineural deafness.
    Sommer A, Young-Wee T, Frye T.
    Am J Med Genet; 1983 May 01; 15(1):71-7. PubMed ID: 6859126
    [Abstract] [Full Text] [Related]

  • 34. Oblique facial clefts: report on 4 Brazilian patients. Evidence for clinical variability and genetic heterogeneity.
    Richieri-Costa A, Gorlin RJ.
    Am J Med Genet; 1994 Nov 15; 53(3):222-6. PubMed ID: 7856656
    [Abstract] [Full Text] [Related]

  • 35. [Associated morphological anomalies of the face and brain in infants].
    Couly G, Aicardi J.
    Arch Fr Pediatr; 1988 Feb 15; 45(2):99-104. PubMed ID: 3389979
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  • 38. Foetal hydantoin syndrome.
    Satpathy R, Bhuyan BK, Das DB, Pant KC, Sarangi J, Pani S.
    J Indian Med Assoc; 1990 Jun 15; 88(6):168-9. PubMed ID: 2230164
    [No Abstract] [Full Text] [Related]

  • 39. A whistling face syndrome case with bilateral skin dimples.
    Buyukavci M, Tan H, Eren S, Balci S.
    Genet Couns; 2005 Jun 15; 16(1):71-3. PubMed ID: 15844782
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