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Journal Abstract Search

250 related items for PubMed ID: 8322809

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  • 2. Aarskog syndrome associated with hypermetropia and toe anomaly.
    Caksen H, Kurtoğlu S, Ciftçi A, Cağil N, Gikrikçi V.
    S Afr Med J; 1997 Dec; 87(12):1699-700. PubMed ID: 9497838
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  • 4. Teebi hypertelorism syndrome: further observations.
    Tsukahara M, Uchida M, Shinohara T.
    Am J Med Genet; 1995 Oct 23; 59(1):59-61. PubMed ID: 8849013
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  • 5. Prenatal sonographic diagnosis of Aarskog syndrome.
    Sepulveda W, Dezerega V, Horvath E, Aracena M.
    J Ultrasound Med; 1999 Oct 23; 18(10):707-10. PubMed ID: 10511304
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  • 7. New syndrome: mother and son with hypertelorism, downslanting palpebral fissures, malar hypoplasia, and apparently low-set ears associated with joint and scrotal anomalies.
    Seaver LH, Cassidy SB.
    Am J Med Genet; 1991 Dec 15; 41(4):405-9. PubMed ID: 1776627
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  • 16. Unusual facies, joint hypermobility, genital anomaly and short stature: a new dysmorphic syndrome.
    Scott CI.
    Birth Defects Orig Artic Ser; 1971 May 15; 7(6):240-6. PubMed ID: 5173168
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  • 17. Autosomal recessive type of whistling face syndrome in twins.
    Kousseff BG, McConnachie P, Hadro TA.
    Pediatrics; 1982 Mar 15; 69(3):328-31. PubMed ID: 7199706
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  • 18. Congenital heart defects in Aarskog syndrome.
    Fernandez I, Tsukahara M, Mito H, Yoshii H, Uchida M, Matsuo K, Kajii T.
    Am J Med Genet; 1994 May 01; 50(4):318-22. PubMed ID: 8209909
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  • 19. Confirmation of the Catania brachydactylous type of acrofacial dysostosis: report of a second family.
    Wulfsberg EA, Campbell AB, Lurie IW, Eanet KR.
    Am J Med Genet; 1996 Jun 28; 63(4):554-7. PubMed ID: 8826434
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  • 20. The Aarskog syndrome.
    Oberiter V, Lovrencić MK, Schmutzer L, Kraus O.
    Acta Paediatr Scand; 1980 Jul 28; 69(4):567-70. PubMed ID: 7446107
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