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Journal Abstract Search

196 related items for PubMed ID: 3300334

  • 21. Occurrence of cardiac malformations in relatives of children with transposition of the great arteries.
    Becker TA, Van Amber R, Moller JH, Pierpont ME.
    Am J Med Genet; 1996 Dec 02; 66(1):28-32. PubMed ID: 8957507
    [Abstract] [Full Text] [Related]

  • 22. Empiric recurrence risk for neural tube defects (NTD) in Krakow region.
    Pietrzyk JJ.
    Acta Anthropogenet; 1983 Dec 02; 7(4):367-72. PubMed ID: 6680315
    [Abstract] [Full Text] [Related]

  • 23. Spina bifida occulta and monozygotic twins.
    Spacca B, Buxton N.
    J Neurosurg Pediatr; 2008 Oct 02; 2(4):258-60. PubMed ID: 18831659
    [Abstract] [Full Text] [Related]

  • 24. The family history of "simple" congenital hydrocephalus. An epidemiological study based on 270 probands.
    Lorber J.
    Z Kinderchir; 1984 Dec 02; 39 Suppl 2():94-5. PubMed ID: 6395547
    [Abstract] [Full Text] [Related]

  • 25. Genetic counseling in families at increased risk for neural tube defects.
    Barganier C, Henson JF, Finley WH.
    Ala J Med Sci; 1985 Jul 02; 22(3):301-4. PubMed ID: 4025720
    [No Abstract] [Full Text] [Related]

  • 26.
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  • 27. [Vertebral involvement and fetal alcohol syndrome].
    de Cornulier M, de Lacour F, Avet-Loiseau H, Passuti N, Branger B, Lemoine P, Picherot G.
    Pediatrie; 1991 Jul 02; 46(10):685-9. PubMed ID: 1662356
    [Abstract] [Full Text] [Related]

  • 28. [Neural tube defects (spina bifida and anencephaly) in Brittany].
    Journel H, Milon J, Dabadie A, Parent P, Roussey M, Le Marec B.
    Pediatrie; 1985 Sep 02; 40(6):461-8. PubMed ID: 3915064
    [Abstract] [Full Text] [Related]

  • 29. [Spina bifida occulta and other neural tube defects. Genetic study and management].
    Robert E.
    Neurochirurgie; 1988 Sep 02; 34 Suppl 1():87-90. PubMed ID: 3054614
    [No Abstract] [Full Text] [Related]

  • 30. [Abnormalities of the neural tube in twins].
    Journel H, Roussey M, Dabadie A, Le Marec B.
    J Gynecol Obstet Biol Reprod (Paris); 1985 Sep 02; 14(7):819-27. PubMed ID: 3912421
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  • 32. Brief clinical report: neural tube defects as an X-linked condition.
    Baraitser M, Burn J.
    Am J Med Genet; 1984 Jan 02; 17(1):383-5. PubMed ID: 6369986
    [Abstract] [Full Text] [Related]

  • 33. Neurologic features of horizontal gaze palsy and progressive scoliosis with mutations in ROBO3.
    Bosley TM, Salih MA, Jen JC, Lin DD, Oystreck D, Abu-Amero KK, MacDonald DB, al Zayed Z, al Dhalaan H, Kansu T, Stigsby B, Baloh RW.
    Neurology; 2005 Apr 12; 64(7):1196-203. PubMed ID: 15824346
    [Abstract] [Full Text] [Related]

  • 34. Etiology of the so-called "idiopathic scoliosis". Biomechanical explanation of spine deformity. Two groups of development of scoliosis. New rehabilitation treatment; possibility of prophylactics.
    Karski T.
    Stud Health Technol Inform; 2002 Apr 12; 91():37-46. PubMed ID: 15457691
    [Abstract] [Full Text] [Related]

  • 35. Split-cord malformation in a girl with Angelman syndrome: a mere coincidence?
    Mastroyianni SD, Kontopoulos E.
    Am J Med Genet; 2002 Jul 22; 111(1):57-60. PubMed ID: 12124736
    [Abstract] [Full Text] [Related]

  • 36. Association of congenital anomalies of the spine and kidneys.
    Tori JA, Dickson JH.
    Clin Orthop Relat Res; 1980 May 22; (148):259-62. PubMed ID: 6991190
    [Abstract] [Full Text] [Related]

  • 37. Neural tube defects in Havana City--incidence and prenatal diagnosis.
    Rodriguez PL, Heredero B, Lopez J, Fernandez Yero JL, Oliva RJ.
    Zentralbl Gynakol; 1982 May 22; 104(20):1325-7. PubMed ID: 6186106
    [Abstract] [Full Text] [Related]

  • 38. Parental age as a risk factor for isolated congenital malformations in a Polish population.
    Materna-Kiryluk A, Wiśniewska K, Badura-Stronka M, Mejnartowicz J, Wieckowska B, Balcar-Boroń A, Czerwionka-Szaflarska M, Gajewska E, Godula-Stuglik U, Krawczyński M, Limon J, Rusin J, Sawulicka-Oleszczuk H, Szwalkiewicz-Warowicka E, Walczak M, Latos-Bieleńska A.
    Paediatr Perinat Epidemiol; 2009 Jan 22; 23(1):29-40. PubMed ID: 19228312
    [Abstract] [Full Text] [Related]

  • 39. 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 Jan 22; 5(2):161-5. PubMed ID: 7917125
    [Abstract] [Full Text] [Related]

  • 40. VACTERL or MURCS association in a girl with neurenteric cyst and identical thoracic malformations in the father: a case of gonosomal mosaicism?
    Orstavik KH, Steen-Johnsen J, Foerster A, Fjeld T, Skullerud K, Lie SO.
    Am J Med Genet; 1992 Aug 01; 43(6):1035-8. PubMed ID: 1415331
    [Abstract] [Full Text] [Related]

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