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Journal Abstract Search

133 related items for PubMed ID: 7573163

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  • 2. Ophthalmic aspects of GAPO syndrome: case report and review.
    Rim PH, Marques-de-Faria AP.
    Ophthalmic Genet; 2005 Sep; 26(3):143-7. PubMed ID: 16272061
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  • 6. Growth retardation, alopecia, pseudo-anodontia, and optic atrophy--the GAPO syndrome: report of a patient and review of the literature.
    Tipton RE, Gorlin RJ.
    Am J Med Genet; 1984 Oct; 19(2):209-16. PubMed ID: 6507471
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  • 7. Ophthalmic findings in GAPO syndrome.
    Ilker SS, Oztürk F, Kurt E, Temel M, Gül D, Sayli BS.
    Jpn J Ophthalmol; 1999 Oct; 43(1):48-52. PubMed ID: 10197743
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  • 9. GAPO syndrome (McKusick 23074)--a connective tissue disorder: report on two affected sibs and on the pathologic findings in the older.
    Wajntal A, Koiffmann CP, Mendonça BB, Epps-Quaglia D, Sotto MN, Rati PB, Opitz JM.
    Am J Med Genet; 1990 Oct; 37(2):213-23. PubMed ID: 2248288
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  • 10. GAPO syndrome: three new Brazilian cases, additional osseous manifestations, and review of the literature.
    Goloni-Bertollo EM, Ruiz MT, Goloni CB, Muniz MP, Valério NI, Pavarino-Bertelli EC.
    Am J Med Genet A; 2008 Jun 15; 146A(12):1523-9. PubMed ID: 18470892
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  • 11. GAPO syndrome in seven new patients: Identification of five novel ANTXR1 mutations including the first large intragenic deletion.
    Abdel-Hamid MS, Ismail S, Zaki MS, Abdel-Salam GMH, Otaify GA, Issa MY, Abdel-Kader M, Girgis M, Aboul-Ezz E, Mazen I, Aglan MS, Temtamy SA.
    Am J Med Genet A; 2019 Feb 15; 179(2):237-242. PubMed ID: 30575274
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  • 13. A novel mutation at ANTXR1 in an Indian patient with growth retardation-alopecia-pseudoanodontia-optic atrophy syndrome.
    Chattopadhyay E, Ghose S, Ray A, Anjum N, Mazumdar A, Roy B.
    Oral Surg Oral Med Oral Pathol Oral Radiol; 2017 Nov 15; 124(5):e261-e265. PubMed ID: 28870703
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  • 16. Telogen hair loss and androgenetic-like alopecia in GAPO syndrome.
    Ahmed B, Gritli S.
    Australas J Dermatol; 2019 May 15; 60(2):e142-e144. PubMed ID: 30255493
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  • 17. GAPO syndrome: first Egyptian case with ultrastructural changes in the gingiva.
    Meguid NA, Afifi HH, Ramzy MI, Hindawy A, Temtamy SA.
    Clin Genet; 1997 Aug 15; 52(2):110-5. PubMed ID: 9298746
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  • 18. GAPO syndrome: report of three affected brothers.
    Gagliardi AR, González CH, Pratesi R.
    Am J Med Genet; 1984 Oct 15; 19(2):217-23. PubMed ID: 6507472
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  • 19. GAPO syndrome: first patients with partially empty sella.
    Orbak Z, Orbak R, Ozkan B, Okten A.
    J Pediatr Endocrinol Metab; 2002 Jun 15; 15(6):865-8. PubMed ID: 12099399
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  • 20. Whole exome sequencing identifies three novel mutations in ANTXR1 in families with GAPO syndrome.
    Bayram Y, Pehlivan D, Karaca E, Gambin T, Jhangiani SN, Erdin S, Gonzaga-Jauregui C, Wiszniewski W, Muzny D, Baylor-Hopkins Center for Mendelian Genomics, Elcioglu NH, Yildirim MS, Bozkurt B, Zamani AG, Boerwinkle E, Gibbs RA, Lupski JR.
    Am J Med Genet A; 2014 Sep 15; 164A(9):2328-34. PubMed ID: 25045128
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