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Journal Abstract Search

121 related items for PubMed ID: 712980

  • 1. Aarskog syndrome. New findings and genetic analysis.
    Escobar V, Weaver DD.
    JAMA; 1978 Dec 08; 240(24):2638-41. PubMed ID: 712980
    [Abstract] [Full Text] [Related]

  • 2. Autosomal dominant inheritance of the Aarskog syndrome.
    Grier RE, Farrington FH, Kendig R, Mamunes P.
    Am J Med Genet; 1983 May 08; 15(1):39-46. PubMed ID: 6344635
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  • 6. New autosomal recessive faciodigitogenital syndrome.
    Teebi AS, Naguib KK, Al-Awadi S, Al-Saleh QA.
    J Med Genet; 1988 Jun 08; 25(6):400-6. PubMed ID: 3398008
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  • 7. The Aarskog syndrome.
    Oberiter V, Lovrencić MK, Schmutzer L, Kraus O.
    Acta Paediatr Scand; 1980 Jul 08; 69(4):567-70. PubMed ID: 7446107
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  • 8. [Aarskog syndrome (author's transl)].
    Kunze J, Spranger J.
    Klin Padiatr; 1973 Nov 08; 185(6):490-4. PubMed ID: 4798676
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  • 9. Prolapse of all cardiac valves in Noonan syndrome.
    Otikunta AN, Subbareddy YV, Polamuri P, Thakkar A.
    BMJ Case Rep; 2015 Feb 25; 2015():. PubMed ID: 25716036
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  • 10. The inheritance of the Aarskog facial-digital-genital syndrome.
    Berman P, Desjardins C, Fraser FC.
    J Pediatr; 1975 Jun 25; 86(6):885-91. PubMed ID: 1127528
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  • 11. Aarskog syndrome in a Danish family: an illustration of the need for dysmorphology in paediatrics.
    Nielsen KB.
    Clin Genet; 1988 Apr 25; 33(4):315-7. PubMed ID: 3359689
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  • 12. [Faciodigitogenital (Aarskog-Scott) syndrome].
    Fragoso R, García-Cruz D, Sánchez-Corona J, Nazará Z, Cantú JM.
    Bol Med Hosp Infant Mex; 1982 Apr 25; 39(4):291-5. PubMed ID: 7093037
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  • 13. Fine mapping of Noonan/cardio-facio cutaneous syndrome in a large family.
    Legius E, Schollen E, Matthijs G, Fryns JP.
    Eur J Hum Genet; 1998 Jan 25; 6(1):32-7. PubMed ID: 9781012
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  • 14. Translocation breakpoint in Aarskog syndrome maps to Xp11.21 between ALAS2 and DXS323.
    Glover TW, Verga V, Rafael J, Barcroft C, Gorski JL, Bawle EV, Higgins JV.
    Hum Mol Genet; 1993 Oct 25; 2(10):1717-8. PubMed ID: 8268928
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  • 15. Clinical confusion of the Noonan syndrome with the Börjeson-Forssman-Lehmann syndrome.
    Preus M.
    J Ment Defic Res; 1984 Sep 25; 28 ( Pt 3)():235-8. PubMed ID: 6492141
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  • 16. A case of Aarskog syndrome with a review of Japanese literature.
    Aihara K, Nishi Y, Usui T.
    Hiroshima J Med Sci; 1982 Jun 25; 31(2):87-90. PubMed ID: 7129954
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  • 17. The Aarskog syndrome in a large family, suggestive for autosomal dominant inheritance.
    van de Vooren MJ, Niermeijer MF, Hoogeboom AJ.
    Clin Genet; 1983 Dec 25; 24(6):439-45. PubMed ID: 6652957
    [Abstract] [Full Text] [Related]

  • 18. The gene for Aarskog syndrome is located between DXS255 and DXS566 (Xp11.2-Xq13).
    Porteous ME, Curtis A, Lindsay S, Williams O, Goudie D, Kamakari S, Bhattacharya SS.
    Genomics; 1992 Oct 25; 14(2):298-301. PubMed ID: 1427846
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  • 19. [Aarskog's syndrome (facial-digital-genital syndrome). Study of a family (author's transl)].
    Scarano G, Rinaldi MM, Cavaliere ML, Esposito M, Sicolo A, Santulli B, Stabile M, Fasano R, Ventruto V.
    Pediatr Med Chir; 1981 Oct 25; 3(4):323-5. PubMed ID: 7343926
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  • 20. Aarskog-Scott syndrome: clinical and molecular characterisation of a family with the coexistence of a novel FGD1 mutation and 16p13.11-p12.3 microduplication.
    Pavone P, Marino S, Maniaci A, Cocuzza S.
    BMJ Case Rep; 2020 Jun 30; 13(6):. PubMed ID: 32606125
    [Abstract] [Full Text] [Related]

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