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Journal Abstract Search

130 related items for PubMed ID: 6107848

  • 1. [Two further cases of faciodigitogenital syndrome (author's transl)].
    Hoo JJ.
    Monatsschr Kinderheilkd; 1980 Sep; 128(9):615-7. PubMed ID: 6107848
    [Abstract] [Full Text] [Related]

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

  • 3. Kuwait type faciodigitogenital syndrome.
    Teebi AS, al Awadi SA.
    J Med Genet; 1991 Nov; 28(11):805. PubMed ID: 1770541
    [No Abstract] [Full Text] [Related]

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

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

  • 6. A familial syndrome of short stature associated with facial dysplasia and genital anomalies.
    Aarskog D.
    Birth Defects Orig Artic Ser; 1971 May; 7(6):235-9. PubMed ID: 4155960
    [Abstract] [Full Text] [Related]

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

  • 8. [Aarskog syndrome. A case report].
    Cincinnati P, Lombardi AM, Morelli M, Rutiloni C.
    Minerva Pediatr; 1994 Sep; 46(9):407-10. PubMed ID: 7799889
    [Abstract] [Full Text] [Related]

  • 9. The Aarskog (facio-digital-genital) syndrome in South Africa. A report of three families.
    de Saxe M, Kromberg JG, Jenkins T.
    S Afr Med J; 1984 Feb 25; 65(8):299-303. PubMed ID: 6695301
    [Abstract] [Full Text] [Related]

  • 10. Fetal face syndrome with acral dysostosis.
    Schinzel A, Zellweger H, Grella A, Prader A.
    Helv Paediatr Acta; 1974 Apr 25; 29(1):55-60. PubMed ID: 4838165
    [No Abstract] [Full Text] [Related]

  • 11. [The tricho-rhino-phalangeal syndrome (author's transl)].
    Lemke T, Pirsig W.
    Laryngol Rhinol Otol (Stuttg); 1978 Dec 25; 57(12):1112-5. PubMed ID: 732492
    [Abstract] [Full Text] [Related]

  • 12. Congenital heart defects in Aarskog syndrome.
    Fernandez I, Tsukahara M, Mito H, Yoshii H, Uchida M, Matsuo K, Kajii T.
    Am J Med Genet; 1994 May 01; 50(4):318-22. PubMed ID: 8209909
    [Abstract] [Full Text] [Related]

  • 13. 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]

  • 14. A previously unrecognized X-linked syndrome of dysmorphia.
    Simpson JL, Landey S, New M, German J.
    Birth Defects Orig Artic Ser; 1975 May 01; 11(2):18-24. PubMed ID: 1227524
    [No Abstract] [Full Text] [Related]

  • 15. Facio-thoraco-genital syndrome: a newly recognized birth defect syndrome.
    Wilf-Miron R, Goodman RM.
    J Craniofac Genet Dev Biol; 1987 May 01; 7(1):19-22. PubMed ID: 3597718
    [Abstract] [Full Text] [Related]

  • 16. The neurofaciodigitorenal (NFDR) syndrome.
    Freire-Maia N, Pinheiro M, Opitz JM.
    Am J Med Genet; 1982 Mar 01; 11(3):329-36. PubMed ID: 7081297
    [Abstract] [Full Text] [Related]

  • 17. [Aarskog's syndrome].
    Hromádková L, Frána L.
    Cesk Oftalmol; 1991 May 01; 47(3):212-8. PubMed ID: 1913912
    [Abstract] [Full Text] [Related]

  • 18. [Trichorhinophalangeal syndrome : analysis of craniofacial architecture in six cases (author's transl)].
    Scheffer P, Verdier M, Finidori G.
    Rev Stomatol Chir Maxillofac; 1981 May 01; 82(4):230-3. PubMed ID: 6944759
    [Abstract] [Full Text] [Related]

  • 19. [Aarskog's syndrome: variable manifestations in men and women].
    Franková Y, Stloukalová M, Rubín A.
    Cesk Pediatr; 1986 Sep 01; 41(9):535-8. PubMed ID: 3769028
    [No Abstract] [Full Text] [Related]

  • 20. The Aarskog syndrome in three brothers.
    Funderburk SJ, Crandall BF.
    Clin Genet; 1974 Sep 01; 6(2):119-24. PubMed ID: 4430151
    [No Abstract] [Full Text] [Related]

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