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Journal Abstract Search

451 related items for PubMed ID: 17266165

  • 41. Complex toe syndactyly with characteristic facial phenotype: a new syndrome?
    Sobreira NL, Cernach MC, Brunoni D, Perez AB.
    Am J Med Genet A; 2008 Jul 01; 146A(13):1725-8. PubMed ID: 18512233
    [Abstract] [Full Text] [Related]

  • 42. Syndactyly, micrognathia and skeletal anomalies: a new syndrome?
    McGaughran J, Moore L, Russell S, Donnai D.
    Clin Dysmorphol; 1998 Apr 01; 7(2):119-22. PubMed ID: 9571282
    [Abstract] [Full Text] [Related]

  • 43. [Amniotic band syndrome and facial malformations].
    Bouguila J, Ben Khoud N, Ghrissi A, Bellalah Z, Belghith A, Landolsi E, Zairi I, Mokhtar M, Adouani A.
    Rev Stomatol Chir Maxillofac; 2007 Dec 01; 108(6):526-9. PubMed ID: 17950767
    [Abstract] [Full Text] [Related]

  • 44. Fraser syndrome: features suggestive of prenatal diagnosis in a review of 38 cases.
    Tessier A, Sarreau M, Pelluard F, André G, Blesson S, Bucourt M, Dechelotte P, Faivre L, Frébourg T, Goldenberg A, Goua V, Jeanne-Pasquier C, Guimiot F, Laquerriere A, Laurent N, Lefebvre M, Loget P, Maréchaud M, Mechler C, Perez MJ, Sabourin JC, Verloes A, Patrier S, Guerrot AM.
    Prenat Diagn; 2016 Dec 01; 36(13):1270-1275. PubMed ID: 27859469
    [Abstract] [Full Text] [Related]

  • 45. [Case report: arhinia and cyclopia in a German Fleckvieh calf].
    Schulze U, Distl O.
    Dtsch Tierarztl Wochenschr; 2006 Jun 01; 113(6):236-9. PubMed ID: 16856611
    [Abstract] [Full Text] [Related]

  • 46. Amniotic band syndrome with significant orofacial clefts and disruptions and distortions of craniofacial structures.
    Muraskas JK, McDonnell JF, Chudik RJ, Salyer KE, Glynn L.
    J Pediatr Surg; 2003 Apr 01; 38(4):635-8. PubMed ID: 12677585
    [Abstract] [Full Text] [Related]

  • 47. Cerebro-oculo-facio-skeletal syndrome: further delineation.
    Gershoni-Baruch R, Ludatscher RM, Lichtig C, Sujov P, Machoul I.
    Am J Med Genet; 1991 Oct 01; 41(1):74-7. PubMed ID: 1951466
    [Abstract] [Full Text] [Related]

  • 48. Rieger syndrome: a case report.
    Dimitrakopoulos J, Voyatzis N, Katopodi T.
    J Oral Maxillofac Surg; 1997 May 01; 55(5):517-21. PubMed ID: 9146524
    [No Abstract] [Full Text] [Related]

  • 49. Two sibs with microcephaly, hygroma colli, renal dysplasia, and cutaneous syndactyly: a new lethal MCA syndrome?
    Janssen HC, Schaap C, Vandevijver N, Moerman P, de Die-Smulders CE, Fryns JP.
    J Med Genet; 1999 Jun 01; 36(6):481-4. PubMed ID: 10874639
    [Abstract] [Full Text] [Related]

  • 50. Prenatal clinical characteristics of Casamassima-Morton-Nance syndrome.
    Aguinaga M, Yllescas E, Canseco M, Machuca A, Acevedo S, Mayén Molina DG.
    Prenat Diagn; 2009 Feb 01; 29(2):175-6. PubMed ID: 19090487
    [No Abstract] [Full Text] [Related]

  • 51. Fraser syndrome: recurrence in a family.
    Singh R, Tandon I, Deo S.
    Indian Pediatr; 2007 Dec 01; 44(12):929-30. PubMed ID: 18175849
    [Abstract] [Full Text] [Related]

  • 52. Two brothers with atypical syndactylies, cerebellar atrophy and severe mental retardation.
    Schorderet DF, Addor MC, Maeder P, Roulet E, Junier L.
    Genet Couns; 2002 Dec 01; 13(4):441-7. PubMed ID: 12558115
    [Abstract] [Full Text] [Related]

  • 53. [Familial hydranencephaly].
    Martin C, Allain D, Vital C, Babin JP, Demarquez JL, San Juan B.
    Ann Pediatr (Paris); 1977 Oct 01; 24(10):673-8. PubMed ID: 16211904
    [No Abstract] [Full Text] [Related]

  • 54. Joubert syndrome associated with patent ductus arteriosus in a newborn infant.
    Peker E, Kirimi E, Sal E, Ceylan A, Ustyol L, Caksen H.
    Genet Couns; 2009 Oct 01; 20(3):289-92. PubMed ID: 19852437
    [No Abstract] [Full Text] [Related]

  • 55. Oblique facial clefts: report on 4 Brazilian patients. Evidence for clinical variability and genetic heterogeneity.
    Richieri-Costa A, Gorlin RJ.
    Am J Med Genet; 1994 Nov 15; 53(3):222-6. PubMed ID: 7856656
    [Abstract] [Full Text] [Related]

  • 56. The cryptophthalmos-syndactyly syndrome. Description, manner of inheritance, and notes on the eye lesions.
    Dinno ND, Edwards WC, Weiskopf B.
    Clin Pediatr (Phila); 1974 Mar 15; 13(3):219 passim. PubMed ID: 4360847
    [No Abstract] [Full Text] [Related]

  • 57. [Meckel-Gruber syndrome].
    Henkel KE, Pfeiffer RA, Stöss H.
    Pathologe; 1993 Jan 15; 14(1):32-5. PubMed ID: 8451225
    [No Abstract] [Full Text] [Related]

  • 58. Cyclotocephaly: severe form of midline malformation association.
    Canki-Klain N.
    Birth Defects Orig Artic Ser; 1993 Jan 15; 29(1):335-43. PubMed ID: 8280885
    [No Abstract] [Full Text] [Related]

  • 59. Roberts syndrome: study of 4 new Rgyptian cases with comparison of clinical and cytogenetic findings.
    Temtamy SA, Ismail S, Helmy NA.
    Genet Couns; 2006 Jan 15; 17(1):1-13. PubMed ID: 16719272
    [Abstract] [Full Text] [Related]

  • 60. On the phenotypic overlap between "severe" oto-palato digital type II syndrome and Larsen syndrome. Variable manifestation of a single autosomal dominant gene.
    Alembik Y, Stoll C, Messer J.
    Genet Couns; 1997 Jan 15; 8(2):133-7. PubMed ID: 9219012
    [Abstract] [Full Text] [Related]

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