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Journal Abstract Search

284 related items for PubMed ID: 16272060

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  • 3. Aarskog syndrome: a case report and literature review.
    Taub MB, Stanton A.
    Optometry; 2008 Jul; 79(7):371-7. PubMed ID: 18577494
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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. Smith-Fineman-Myers syndrome: report of a third case.
    Stephenson LD, Johnson JP.
    Am J Med Genet; 1985 Oct 15; 22(2):301-4. PubMed ID: 4050861
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  • 9. Clinical variation of Aarskog syndrome in a large family with 2189delA in the FGD1 gene.
    Shalev SA, Chervinski E, Weiner E, Mazor G, Friez MJ, Schwartz CE.
    Am J Med Genet A; 2006 Jan 15; 140(2):162-5. PubMed ID: 16353258
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  • 10. Genomic organization of the faciogenital dysplasia (FGD1; Aarskog syndrome) gene.
    Pasteris NG, Buckler J, Cadle AB, Gorski JL.
    Genomics; 1997 Aug 01; 43(3):390-4. PubMed ID: 9268645
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  • 12. 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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  • 13. Prenatal sonographic diagnosis of Aarskog syndrome.
    Sepulveda W, Dezerega V, Horvath E, Aracena M.
    J Ultrasound Med; 1999 Oct 01; 18(10):707-10. PubMed ID: 10511304
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  • 14. 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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  • 17. Dental and craniofacial features of Aarskog syndrome: report of a case and review of literature.
    Reddy P, Kharbanda OP, Kabra M, Duggal R.
    J Clin Pediatr Dent; 1999 Dec 15; 23(2):155-9. PubMed ID: 10204459
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  • 18. Autosomal recessive Robinow syndrome.
    Teebi AS.
    Am J Med Genet; 1990 Jan 15; 35(1):64-8. PubMed ID: 2301471
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  • 19. An intragenic TaqI polymorphism in the faciogenital dysplasia (FGD1) locus, the gene responsible for Aarskog syndrome.
    Pasteris NG, Gorski JL.
    Hum Genet; 1995 Oct 15; 96(4):494. PubMed ID: 7557980
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  • 20. [Aarskog syndrome. A case report].
    Cincinnati P, Lombardi AM, Morelli M, Rutiloni C.
    Minerva Pediatr; 1994 Sep 15; 46(9):407-10. PubMed ID: 7799889
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