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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

179 related items for PubMed ID: 8256802

  • 21. New manifestations in an infant with Neu Laxova syndrome.
    Rouzbahani L.
    Am J Med Genet; 1995 Mar 27; 56(2):239-40. PubMed ID: 7625453
    [No Abstract] [Full Text] [Related]

  • 22. Optiz trigonocephaly syndrome: report of two cases.
    Flatz SD, Schinzel A, Doehring E, Kamran D, Eilers E.
    Eur J Pediatr; 1984 Jan 27; 141(3):183-5. PubMed ID: 6698065
    [Abstract] [Full Text] [Related]

  • 23. Two siblings with midline field defects and Hirschsprung disease: variable expression of Toriello-Carey or new syndrome?
    Jespers A, Buntinx I, Melis K, Vaerenberg M, Janssens G.
    Am J Med Genet; 1993 Aug 15; 47(2):299-302. PubMed ID: 8213924
    [Abstract] [Full Text] [Related]

  • 24. Diffuse polymicrogyria associated with an unusual pattern of multiple congenital anomalies including turribrachycephaly and hypogenitalism.
    Cohn RD, Gillessen-Kaesbach G, Dobyns WB, Kahn T, Lenard HG, Voit T.
    Am J Med Genet; 1996 May 03; 63(1):314-7. PubMed ID: 8723127
    [Abstract] [Full Text] [Related]

  • 25. Case report and delineation of the congenital hypothalamic hamartoblastoma syndrome (Pallister-Hall syndrome).
    Iafolla K, Fratkin JD, Spiegel PK, Cohen MM, Graham JM.
    Am J Med Genet; 1989 Aug 03; 33(4):489-99. PubMed ID: 2688416
    [Abstract] [Full Text] [Related]

  • 26. Toriello-Carey syndrome in a Turkish newborn.
    Uras N, Sandal G, Oguz S, Aydemir O, Erdeve O, Dilmen U.
    Genet Couns; 2009 Aug 03; 20(3):243-7. PubMed ID: 19852430
    [Abstract] [Full Text] [Related]

  • 27. Peters'-Plus syndrome with agenesis of the corpus callosum: report of a case and confirmation of autosomal recessive inheritance.
    Camera G, Centa A, Pozzolo S, Camera A.
    Clin Dysmorphol; 1993 Oct 03; 2(4):317-21. PubMed ID: 8305962
    [Abstract] [Full Text] [Related]

  • 28. Cleft lip and palate, characteristic facial appearance, malrotation of the intestine, and lethal congenital heart disease in two sibs: a new autosomal recessive condition?
    McPherson E, Clemens M.
    Am J Med Genet; 1996 Mar 01; 62(1):58-60. PubMed ID: 8779326
    [Abstract] [Full Text] [Related]

  • 29. [A genetic study and clinical classification of 154 cases of mandibulofacial dystosis (Franceschetti's syndrome), with descriptions of associated malformations].
    Vatré JL.
    J Genet Hum; 1971 Mar 01; 19(1):17-100. PubMed ID: 5003458
    [No Abstract] [Full Text] [Related]

  • 30. New X-linked mental retardation syndrome with the gene mapped tentatively in Xp22.3.
    Wittwer B, Kircheisen R, Leutelt J, Orth U, Gal A.
    Am J Med Genet; 1996 Jul 12; 64(1):42-9. PubMed ID: 8826447
    [Abstract] [Full Text] [Related]

  • 31. "C" trigonocephaly syndrome with diaphragmnatic hernia.
    Addor MC, Stefanutti D, Farron F, Meinecke P, Lacombe D, Sarlangue J, Prescia G, Schorderet DF.
    Genet Couns; 1995 Jul 12; 6(2):113-20. PubMed ID: 7546453
    [Abstract] [Full Text] [Related]

  • 32. Syndrome of mental retardation, cleft palate, eventration of diaphragm, congenital heart defect, glaucoma, growth failure and craniosynostosis.
    Lowry RB, MacLean JR.
    Birth Defects Orig Artic Ser; 1977 Jul 12; 13(3B):203-28. PubMed ID: 890093
    [Abstract] [Full Text] [Related]

  • 33. Filippi syndrome: a specific MCA/MR complex within the spectrum of so called "craniodigital syndromes". Report of an additional patient with a peculiar mpp and review of the literature.
    Franceschini P, Licata D, Guala A, Di Cara G, Franceschini D.
    Genet Couns; 2002 Jul 12; 13(3):343-52. PubMed ID: 12416644
    [Abstract] [Full Text] [Related]

  • 34. Previously undescribed syndrome of craniofacial, hand anomalies, and sensorineural deafness.
    Sommer A, Young-Wee T, Frye T.
    Am J Med Genet; 1983 May 12; 15(1):71-7. PubMed ID: 6859126
    [Abstract] [Full Text] [Related]

  • 35. Toriello-Carey syndrome in a patient with a de novo balanced translocation [46,XY,t(2;14)(q33;q22)] interrupting SATB2.
    Tegay DH, Chan KK, Leung L, Wang C, Burkett S, Stone G, Stanyon R, Toriello HV, Hatchwell E.
    Clin Genet; 2009 Mar 12; 75(3):259-64. PubMed ID: 19170718
    [Abstract] [Full Text] [Related]

  • 36. A third patient with median cleft upper lip, mental retardation and pugilistic facies (W syndrome): corroboration of a hitherto private syndrome.
    Bottani A, Schinzel A.
    Clin Dysmorphol; 1993 Jul 12; 2(3):225-31. PubMed ID: 8287184
    [Abstract] [Full Text] [Related]

  • 37. Frontonasal dysplasia, macroblepharon, eyelid colobomas, ear anomalies, macrostomia, mental retardation, and CNS structural anomalies. A new syndrome?
    Guion-Almeida ML, Richieri-Costa A.
    Clin Dysmorphol; 1999 Jan 12; 8(1):1-4. PubMed ID: 10327243
    [Abstract] [Full Text] [Related]

  • 38. New dominant syndrome of pterygium colli, mental retardation, and digital anomalies.
    Khalifa MM, Graham G.
    Am J Med Genet; 1994 Aug 01; 52(1):55-7. PubMed ID: 7977463
    [Abstract] [Full Text] [Related]

  • 39. 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]

  • 40. A syndrome of facial dysmorphia, birth defects, myelodysplasia and immunodeficiency in three sibs of consanguineous parents.
    Stoll C, Alembik Y, Lutz P.
    Genet Couns; 1994 Jun 15; 5(2):161-5. PubMed ID: 7917125
    [Abstract] [Full Text] [Related]

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