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Journal Abstract Search

130 related items for PubMed ID: 6107848

  • 41. Conductive deafness, symphalangism, and facial abnormalities: the WL syndrome in a Japanese family.
    Higashi K, Inoue S.
    Am J Med Genet; 1983 Sep; 16(1):105-9. PubMed ID: 6638061
    [Abstract] [Full Text] [Related]

  • 42. Desbuquois syndrome: three further cases and review of the literature.
    Gillessen-Kaesbach G, Meinecke P, Ausems MG, Nöthen M, Albrecht B, Beemer FA, Zerres K.
    Clin Dysmorphol; 1995 Apr; 4(2):136-44. PubMed ID: 7606320
    [Abstract] [Full Text] [Related]

  • 43. New dominant syndrome of microcephaly, facial abnormalities, micromelia, and mental retardation.
    Tsukahara M, Sugio Y.
    J Hum Genet; 1998 Apr; 43(4):224-7. PubMed ID: 9852671
    [Abstract] [Full Text] [Related]

  • 44. Guadalajara camptodactyly syndrome. A distinct probably autosomal recessive disorder.
    Cantú JM, Rivera H, Nazará Z, Rojas Q, Hernández A, García-Cruz D.
    Clin Genet; 1980 Sep; 18(3):153-9. PubMed ID: 7192193
    [Abstract] [Full Text] [Related]

  • 45. [Fetal face syndrome (Robinow syndrome].
    Zizka J, Gayer J, Jüttnerová V, Balícek P, Tesarová B.
    Cesk Pediatr; 1981 Jun; 36(6):328-30. PubMed ID: 7273217
    [No Abstract] [Full Text] [Related]

  • 46. Characteristic facies in type B brachydactyly?
    Houlston RS, Temple IK.
    Clin Dysmorphol; 1994 Jul; 3(3):224-7. PubMed ID: 7981857
    [Abstract] [Full Text] [Related]

  • 47. Variable expressivity in the trichorhinophalangeal syndrome type I.
    Frias JL, Felman AH, Garnica AD, Wallace SE.
    Birth Defects Orig Artic Ser; 1979 Jul; 15(5B):361-72. PubMed ID: 526590
    [No Abstract] [Full Text] [Related]

  • 48. Dental and Maxillofacial Signs in Aarskog Syndrome: A Review of 3 Siblings and the Literature.
    Depeyre A, Schlund M, Gryseleyn R, Ferri J.
    J Oral Maxillofac Surg; 2018 Oct; 76(10):2202-2208. PubMed ID: 29689188
    [Abstract] [Full Text] [Related]

  • 49. Apparently new syndrome of short stature, lumbar malsegmentation, and minor facial anomalies in two brothers.
    Leipälä JA, Kaitila I.
    Am J Med Genet; 1994 Aug 01; 52(1):103-7. PubMed ID: 7977451
    [Abstract] [Full Text] [Related]

  • 50. Facial and oral findings in trichorhinophalangeal syndrome type 1 (characteristics of TRPS 1).
    Bennett CG, Hill CJ, Frias JL.
    Pediatr Dent; 1981 Dec 01; 3(4):348-52. PubMed ID: 6952172
    [No Abstract] [Full Text] [Related]

  • 51. Lethal congenital non-spherocytic, non-immune hemolytic anemia with genital and other anomalies in two brothers.
    Waters BL, West BR.
    Am J Med Genet; 1995 Jan 30; 55(3):319-24. PubMed ID: 7726230
    [Abstract] [Full Text] [Related]

  • 52. Russell-Silver syndrome: a study of 3 cases.
    Kulkarni ML, Venkataramana V, Sureshkumar C, Shabeer HM.
    Ann Dent; 1995 Jan 30; 54(1-2):56-60. PubMed ID: 8572550
    [Abstract] [Full Text] [Related]

  • 53. [Structural abnormalities of Y chromosome: study of 13 cases (author's transl)].
    Vincent A, Gendrel D, Chaussain JL, Canlorbe P, Job JC.
    Ann Pediatr (Paris); 1981 Mar 30; 28(3):205-8. PubMed ID: 7224569
    [No Abstract] [Full Text] [Related]

  • 54. Picture of the month: Fetal face syndrome (Robinow Snydrome).
    Gellis SS, Feingold M, Bull M.
    Am J Dis Child; 1975 Mar 30; 129(3):351-2. PubMed ID: 1121964
    [No Abstract] [Full Text] [Related]

  • 55. Total anonychia congenita and microcephaly with normal intelligence: a new autosomal-recessive syndrome?
    Teebi AS, Kaurah P.
    Am J Med Genet; 1996 Dec 18; 66(3):257-60. PubMed ID: 8985482
    [Abstract] [Full Text] [Related]

  • 56. [The fetal face syndrome or Robinow syndrome. Description of a case (clinical and immunological aspects)].
    Marni E, Monafo V, Zanol MG, Pedroni E.
    Minerva Pediatr; 1980 Jan 15; 32(1):47-52. PubMed ID: 7254142
    [No Abstract] [Full Text] [Related]

  • 57.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 58. [Complex of multiple malformations in two unrelated children (author's transl)].
    Pfeiffer RA, Müller H.
    Padiatr Padol; 1971 Jan 15; 6(3):262-7. PubMed ID: 5164141
    [No Abstract] [Full Text] [Related]

  • 59.
    ; . PubMed ID:
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  • 60. Syndactyly of the ring and small finger.
    De Smet L, Mulier T, Fabry G.
    Genet Couns; 1994 Jan 15; 5(1):45-9. PubMed ID: 8031535
    [Abstract] [Full Text] [Related]

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