These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

202 related items for PubMed ID: 1127528

  • 1. The inheritance of the Aarskog facial-digital-genital syndrome.
    Berman P, Desjardins C, Fraser FC.
    J Pediatr; 1975 Jun; 86(6):885-91. PubMed ID: 1127528
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 3. The Aarskog syndrome in a large family, suggestive for autosomal dominant inheritance.
    van de Vooren MJ, Niermeijer MF, Hoogeboom AJ.
    Clin Genet; 1983 Dec 15; 24(6):439-45. PubMed ID: 6652957
    [Abstract] [Full Text] [Related]

  • 4. The facial-digital-genital (Aarskog) syndrome.
    Sugarman GI, Rimoin DL, Lachman RS.
    Am J Dis Child; 1973 Aug 15; 126(2):248-52. PubMed ID: 4146757
    [No Abstract] [Full Text] [Related]

  • 5. New autosomal recessive faciodigitogenital syndrome.
    Teebi AS, Naguib KK, Al-Awadi S, Al-Saleh QA.
    J Med Genet; 1988 Jun 15; 25(6):400-6. PubMed ID: 3398008
    [Abstract] [Full Text] [Related]

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. 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
    [Abstract] [Full Text] [Related]

  • 8. The Aarskog (facio-digito-genital) syndrome.
    Hoo JJ.
    Clin Genet; 1979 Oct 09; 16(4):269-76. PubMed ID: 519896
    [Abstract] [Full Text] [Related]

  • 9. Autosomal dominant inheritance of the Aarskog syndrome.
    Grier RE, Farrington FH, Kendig R, Mamunes P.
    Am J Med Genet; 1983 May 09; 15(1):39-46. PubMed ID: 6344635
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. The Aarskog syndrome.
    Oberiter V, Lovrencić MK, Schmutzer L, Kraus O.
    Acta Paediatr Scand; 1980 Jul 09; 69(4):567-70. PubMed ID: 7446107
    [Abstract] [Full Text] [Related]

  • 13. Autosomal recessive malformation syndrome with minor manifestation in the heterozygotes: a preliminary report of a possible new syndrome.
    Paes-Alves AF, Azevêdo ES, Sousa MG, Almeida-Melo N, Oliveira-Filho OJ.
    Am J Med Genet; 1991 Nov 01; 41(2):141-52. PubMed ID: 1785624
    [Abstract] [Full Text] [Related]

  • 14. 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
    [Abstract] [Full Text] [Related]

  • 15. Inheritance of the Aarskog syndrome.
    Berman P, Desjardins C, Fraser FC.
    Birth Defects Orig Artic Ser; 1974 Oct 01; 10(7):151-9. PubMed ID: 4153991
    [No Abstract] [Full Text] [Related]

  • 16. Unusual facies, joint hypermobility, genital anomaly and short stature: a new dysmorphic syndrome.
    Scott CI.
    Birth Defects Orig Artic Ser; 1971 May 01; 7(6):240-6. PubMed ID: 5173168
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. A new autosomal recessive syndrome characterized by ocular hypertelorism, distinctive face, mental retardation, brachydactyly, and genital abnormalities.
    Spiegel R, Horovitz Y, Peters H, Erdogan F, Chervinsky I, Shalev SA.
    Am J Med Genet A; 2009 Dec 01; 149A(12):2655-60. PubMed ID: 19938075
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. Acro-fronto-facio-nasal dysostosis: report of a new Brazilian family.
    Richieri-Costa A, Guion-Almeida ML, Pagnan NA.
    Am J Med Genet; 1992 Dec 01; 44(6):800-2. PubMed ID: 1481850
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 11.