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Journal Abstract Search

162 related items for PubMed ID: 10511304

  • 1. Prenatal sonographic diagnosis of Aarskog syndrome.
    Sepulveda W, Dezerega V, Horvath E, Aracena M.
    J Ultrasound Med; 1999 Oct; 18(10):707-10. PubMed ID: 10511304
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  • 2. Aarskog syndrome: report of a family with review and discussion of nosology.
    Teebi AS, Rucquoi JK, Meyn MS.
    Am J Med Genet; 1993 Jun 15; 46(5):501-9. PubMed ID: 8322809
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  • 3. Aarskog syndrome associated with hypermetropia and toe anomaly.
    Caksen H, Kurtoğlu S, Ciftçi A, Cağil N, Gikrikçi V.
    S Afr Med J; 1997 Dec 15; 87(12):1699-700. PubMed ID: 9497838
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  • 5. A novel mutation in a mother and a son with Aarskog-Scott syndrome.
    Altıncık A, Kaname T, Demir K, Böber E.
    J Pediatr Endocrinol Metab; 2013 Dec 15; 26(3-4):385-8. PubMed ID: 23443263
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  • 6. The Aarskog syndrome.
    Oberiter V, Lovrencić MK, Schmutzer L, Kraus O.
    Acta Paediatr Scand; 1980 Jul 15; 69(4):567-70. PubMed ID: 7446107
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  • 7. Ocular and systemic findings in the Aarskog (facial-digital-genital) syndrome.
    Brodsky MC, Keppen LD, Rice CD, Ranells JD.
    Am J Ophthalmol; 1990 Apr 15; 109(4):450-6. PubMed ID: 2330948
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  • 8. The Aarskog syndrome.
    Fryns JP, Macken J, Vinken L, Igodt-Ameye L, van den Berghe H.
    Hum Genet; 1978 Jun 09; 42(2):129-35. PubMed ID: 669698
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  • 10. Tortuosity of the retinal vessels in Aarskog syndrome (faciogenital dysplasia).
    Pizio HF, Scott MH, Richard JM.
    Ophthalmic Genet; 1994 Mar 09; 15(1):37-40. PubMed ID: 7953251
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  • 11. Dental and Maxillofacial Signs in Aarskog Syndrome: A Review of 3 Siblings and the Literature.
    Depeyre A, Schlund M, Gryseleyn R, Ferri J.
    J Oral Maxillofac Surg; 2018 Oct 09; 76(10):2202-2208. PubMed ID: 29689188
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  • 15. Unusual facies, joint hypermobility, genital anomaly and short stature: a new dysmorphic syndrome.
    Scott CI.
    Birth Defects Orig Artic Ser; 1971 May 09; 7(6):240-6. PubMed ID: 5173168
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  • 16. Geleophysic dysplasia: a report of three affected boys--prenatal ultrasound does not detect recurrence.
    Rosser EM, Wilkinson AR, Hurst JA, McGaughran JM, Donnai D.
    Am J Med Genet; 1995 Sep 11; 58(3):217-21. PubMed ID: 8533820
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  • 18. A novel splice site mutation of FGD1 gene in an Aarskog-Scott syndrome patient with a large anterior fontanel.
    Parıltay E, Hazan F, Ataman E, Demir K, Etlik Ö, Özbek E, Özkan B.
    J Pediatr Endocrinol Metab; 2016 Sep 01; 29(9):1111-4. PubMed ID: 27544718
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  • 19. Congenital diaphragmatic hernia and genital anomalies: Emanuel syndrome.
    Gremeau AS, Coste K, Blanc P, Goumy C, Francannet C, Dechelotte PJ, Vago P, Laurichesse-Delmas H, Labbe A, Lemery D, Sapin V, Gallot D.
    Prenat Diagn; 2009 Aug 01; 29(8):816-8. PubMed ID: 19434659
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  • 20. The facio-digito-genital syndrome (Aarskog syndrome): a further delineation of the distinct radiological findings.
    Lizcano-Gil LA, Garcia-Cruz D, Cantu JM, Fryns JP.
    Genet Couns; 1994 Aug 01; 5(4):387-92. PubMed ID: 7888143
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