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Journal Abstract Search

143 related items for PubMed ID: 2494224

  • 21. 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
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  • 22. [Congenital glaucoma with dominant heredity associated with ocular and somatic malformations (Rieger's syndrome)].
    Deimarcelle Y.
    Ann Ocul (Paris); 1968 Feb; 201(2):132-57. PubMed ID: 4970667
    [No Abstract] [Full Text] [Related]

  • 23. Rieger's syndrome.
    Tewari S, Govila CP, Garg AP.
    J Oral Pathol Med; 1991 Nov; 20(10):514-5. PubMed ID: 1753356
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  • 25. [A new sublethal syndrome with multiple malformations associating diaphragmatic hernia, distal digital hypoplasia, and craniofacial anomalies. The "Fryns syndrome"].
    Fryns JP, Moerman P, Van den Berghe H, Aymé S.
    J Genet Hum; 1989 Sep; 37(3):203-5. PubMed ID: 2625623
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  • 26. [Variability of clinical manifestations in the family with Axenfeld-Rieger syndrome].
    Kamińska A, Sokołowska-Oracz A, Pawluczyk-Dyjecińska M, Szaflik JP.
    Klin Oczna; 2007 Sep; 109(7-9):321-6. PubMed ID: 18260289
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  • 31. Rieger's syndrome.
    Kumta NB, Agarwal U, Savliwala AS.
    Indian Pediatr; 1982 Feb; 19(2):183-5. PubMed ID: 6811430
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  • 34. Schinzel acrocallosal syndrome: a variant example of the Greig syndrome?
    Legius E, Fryns JP, Casaer P, Boel M, Eggermont E.
    Ann Genet; 1985 Feb; 28(4):239-40. PubMed ID: 3879437
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  • 35. Mental retardation, short stature, almond-shaped eyes, small downturned mouth and coned epiphyses: a new case of Hunter-Fraser syndrome.
    Van Maldergem L, Gillerot Y, Perlmutter N, Wetzburger C, Koulischer L.
    Am J Med Genet; 1990 Oct; 37(2):283-5. PubMed ID: 2248298
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  • 37. Syndrome identification case report 90: multiple craniofacial and skeletal defects.
    Mastroiacovo P, De Rosa G, Satta MA, Colavita N, Priolo F, Pasargiklian E.
    J Clin Dysmorphol; 1983 Oct; 1(1):13-5. PubMed ID: 6580383
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  • 39. 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
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  • 40. Conductive deafness, symphalangism, and facial abnormalities: the WL syndrome in a Japanese family.
    Higashi K, Inoue S.
    Am J Med Genet; 1983 Sep 01; 16(1):105-9. PubMed ID: 6638061
    [Abstract] [Full Text] [Related]

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