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Journal Abstract Search

174 related items for PubMed ID: 6954841

  • 21. [Aarskog's facio-digital-genital syndrome. Clinical contribution].
    Larpi P, Savanelli A, Cigliano B, De Fazio P, Vecchio P, Esposito P.
    Minerva Chir; ; 40(23-24):1689-92. PubMed ID: 2870446
    [No Abstract] [Full Text] [Related]

  • 22. X-linked recessive inheritance of an orofaciodigital syndrome with partial expression in females and survival of affected males.
    Edwards M, Mulcahy D, Turner G.
    Clin Genet; 1988 Nov; 34(5):325-32. PubMed ID: 3229001
    [Abstract] [Full Text] [Related]

  • 23. [Papillon-Lége and Psaume orofaciodigital syndrome (OFD syndrome)].
    Felgenhauer WR, Farquet M, Ferrier PE.
    Arch Genet (Zur); 1972 Nov; 45(2):65-87. PubMed ID: 4657589
    [No Abstract] [Full Text] [Related]

  • 24. [Papillon-Leagre and Psaume syndrome in 4 sisters].
    Vaillaud JC, de Swarte M, Vaillant JM, Szepetowski G, Martin J.
    Lyon Med; 1969 Jun 22; 221(25):1499-503. PubMed ID: 5360860
    [No Abstract] [Full Text] [Related]

  • 25. [Oto-palato-digital type I syndrome in five generations. Relationship to the type II form].
    Le Marec B, Odent S, Bracq E, Bulard MB, Bourdinière J, Babut JM.
    Ann Genet; 1988 Jun 22; 31(3):155-61. PubMed ID: 3265608
    [Abstract] [Full Text] [Related]

  • 26. Discordance in monozygotic twins for aglossia-adactylia, and possible clues to the pathogenesis of the syndrome.
    Robinow M, Marsh JL, Edgerton MT, Sabio H, Johnson GF.
    Birth Defects Orig Artic Ser; 1978 Jun 22; 14(6A):223-30. PubMed ID: 569511
    [No Abstract] [Full Text] [Related]

  • 27. Familial orofaciodigital syndrome type I presenting as adult polycystic kidney disease.
    Donnai D, Kerzin-Storrar L, Harris R.
    J Med Genet; 1987 Feb 22; 24(2):84-7. PubMed ID: 3560172
    [Abstract] [Full Text] [Related]

  • 28. [Orofaciodigital syndrome (types I and II)].
    Fukuyama Y.
    Nihon Rinsho; 1977 Feb 22; 35 Suppl 1():622-3. PubMed ID: 612923
    [No Abstract] [Full Text] [Related]

  • 29. Orofaciodigital syndrome, type I: a phenotypic and genetic analysis.
    Melnick M, Shields ED.
    Oral Surg Oral Med Oral Pathol; 1975 Nov 22; 40(5):599-610. PubMed ID: 1059061
    [Abstract] [Full Text] [Related]

  • 30. [How are the Blaschko lines arranged on the scalp?].
    Happle R, Fuhrmann-Rieger A, Fuhrmann W.
    Hautarzt; 1984 Jul 22; 35(7):366-9. PubMed ID: 6469640
    [Abstract] [Full Text] [Related]

  • 31. Orofaciodigital syndrome I: a case report.
    Gunbay S, Zeytinoglu B, Ozkinay F, Ozkinay C, Oncag A.
    J Clin Pediatr Dent; 1996 Jul 22; 20(4):329-32. PubMed ID: 9151628
    [Abstract] [Full Text] [Related]

  • 32. [The orofaciodigital syndrome].
    Lehnert S.
    Dtsch Zahnarztl Z; 1969 Jul 22; 24(11):993-1002. PubMed ID: 5261948
    [No Abstract] [Full Text] [Related]

  • 33. The oro-facial-digital syndrome.
    Whelan DT, Feldman W, Dost I.
    Clin Genet; 1975 Sep 22; 8(3):205-12. PubMed ID: 1175324
    [Abstract] [Full Text] [Related]

  • 34. [FG syndrome: report of 4 cases with agenesis of the corpus callosum].
    Lacassie Y, Blanco B, Boehme V, Norambuena A.
    Rev Chil Pediatr; 1986 Sep 22; 57(6):531-6. PubMed ID: 3671828
    [No Abstract] [Full Text] [Related]

  • 35. [Tooth and oral mucosa hereditary anomalies in complex syndromes characterized by hyper- or hypotrichosis].
    Giannetti L, Consolo U, Bambini F.
    Minerva Stomatol; 2003 Sep 22; 52(1-2):25-30. PubMed ID: 12686911
    [Abstract] [Full Text] [Related]

  • 36.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 37. [The diagnosis of Cohen's syndrome].
    Krajewska-Walasek M, Chrzanowska K, Rump Z.
    Wiad Lek; 1986 Sep 15; 39(18):1270-7. PubMed ID: 3564466
    [No Abstract] [Full Text] [Related]

  • 38. [The orofaciodigital syndrome. The Papillon-Léage-Psaume syndrome].
    Koberg W, Schettler D.
    Dtsch Zahnarztl Z; 1969 Sep 15; 24(11):1002-7. PubMed ID: 5261935
    [No Abstract] [Full Text] [Related]

  • 39. [2 cases of orofacial digital syndrome in a mother and daughter].
    Sibora P, Krajka R, Ksiezopolska A.
    Czas Stomatol; 1979 Sep 15; 32(10):933-6. PubMed ID: 292544
    [No Abstract] [Full Text] [Related]

  • 40. [Mohr syndrome. Signs and genetic counseling].
    Herrmann FH, Raschke N, Herrmann MC.
    Kinderarztl Prax; 1981 Sep 15; 49(9):479-85. PubMed ID: 7300134
    [No Abstract] [Full Text] [Related]

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