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Journal Abstract Search

193 related items for PubMed ID: 7205201

  • 41. Prenatal diagnosis of Meckel syndrome.
    Leschot NJ, de Nef JJ, Becker-Bloemkolk MJ, Verjaal M, Wiesenhaan PF.
    Hum Genet; 1978 Sep 19; 43(3):333-6. PubMed ID: 81169
    [Abstract] [Full Text] [Related]

  • 42. Spectrum of anomalies in the Meckel syndrome, or: "Maybe there is a malformation syndrome with at least one constant anomaly".
    Fraser FC, Lytwyn A.
    Am J Med Genet; 1981 Sep 19; 9(1):67-73. PubMed ID: 7246621
    [Abstract] [Full Text] [Related]

  • 43. Phenotypic variability in Meckel-Gruber syndrome.
    Farag TI, Usha R, Uma R, Mady SA, al-Nagdy K, el-Badramany MH.
    Clin Genet; 1990 Sep 19; 38(3):176-9. PubMed ID: 2225527
    [Abstract] [Full Text] [Related]

  • 44. Encephalocele, polycystic kidneys, and polydactyly as an autosomal recessive trait simulating certain other disorders: the Meckel syndrome.
    Mecke S, Passarge E.
    Ann Genet; 1971 Jun 19; 14(2):97-103. PubMed ID: 4997715
    [No Abstract] [Full Text] [Related]

  • 45. [Prenatal diagnosis of Potter syndrome].
    Csécsei K, Tóth Z, Szeifert G, Tankó A, Nagy J, Papp Z.
    Orv Hetil; 1986 Feb 02; 127(5):271-5. PubMed ID: 3513085
    [No Abstract] [Full Text] [Related]

  • 46. Ultrasound and genetic counselling in the prenatal diagnosis of fetal malformations.
    Pachì A, Maggi E, Giancotti A, Torcia F, Giampà G, Forleo S.
    J Perinat Med; 1991 Feb 02; 19 Suppl 1():50-61. PubMed ID: 1779397
    [No Abstract] [Full Text] [Related]

  • 47. Prenatal diagnosis of Meckel syndrome.
    Patel ZM, Iyer SS, Khatkatay MI, Mandlekar A, Baxi AJ, Pai RR, Joshi UM, Ambani LM.
    Indian Pediatr; 1981 Oct 02; 18(10):762-3. PubMed ID: 7327716
    [No Abstract] [Full Text] [Related]

  • 48. [The Meckel-syndrome in a newborn].
    Göcke H, Muradow I, Eldering G, Gullotta F.
    Geburtshilfe Frauenheilkd; 1982 Aug 02; 42(8):602-4. PubMed ID: 6922811
    [No Abstract] [Full Text] [Related]

  • 49. Meckel Gruber syndrome: occurrence in non-consanguineous marriages.
    de Silva MV, Senanayake H, Siriwardana KD.
    Ceylon Med J; 2004 Mar 02; 49(1):30-1. PubMed ID: 15255329
    [Abstract] [Full Text] [Related]

  • 50. Editorial comment: variability in the Smith-Lemli-Opitz syndrome: overlap with the Meckel syndrome.
    Lowry RB.
    Am J Med Genet; 1983 Mar 02; 14(3):429-33. PubMed ID: 6859094
    [No Abstract] [Full Text] [Related]

  • 51. [Meckel-Gruber syndrome].
    Flessa A, Rempen A, Schmausser B, Marx A.
    Z Geburtshilfe Neonatol; 1996 Mar 02; 200(2):66-8. PubMed ID: 8767290
    [Abstract] [Full Text] [Related]

  • 52. [Prenatal diagnosis of pulmonary hypoplasia camptodactyly syndrome. Hypothesis concerning the origin of hydramnios].
    Lopes P, Talmant C, Cohen JY, Mouzard A, Nomballais MF, Boiffard JP, Lerat MF.
    J Genet Hum; 1985 Sep 02; 33(3-4):347-55. PubMed ID: 3903053
    [Abstract] [Full Text] [Related]

  • 53. Prenatal diagnosis of polycystic kidneys and encephalocele (Meckel syndrome).
    Friedrich U, Hansen KB, Hauge M, Hägerstrand I, Kristoffersen K, Ludvigsen E, Merrild U, Nørgaard-Pedersen B, Petersen GB, Therkelsen AJ.
    Clin Genet; 1979 Mar 02; 15(3):278-86. PubMed ID: 84722
    [Abstract] [Full Text] [Related]

  • 54. Prenatal diagnosis of Meckel-Gruber syndrome case reports.
    Su SL, Liu CM, Lee JN.
    Gaoxiong Yi Xue Ke Xue Za Zhi; 1995 Feb 02; 11(2):127-32. PubMed ID: 7707455
    [Abstract] [Full Text] [Related]

  • 55. Meckel Gruber syndrome: a case diagnosed in utero.
    Balci S, Onol B, Erçal MD, Beksaç S, Erzen C, Akhan O.
    Turk J Pediatr; 1992 Feb 02; 34(3):179-85. PubMed ID: 1485386
    [Abstract] [Full Text] [Related]

  • 56. Prenatal diagnosis of renal anomalies.
    Kaffe S, Rose JS, Godmilow L, Walker BA, Kerenyi T, Beratis N, Reyes P, Hirschhorn K.
    Am J Med Genet; 1977 Feb 02; 1(2):241-51. PubMed ID: 610432
    [Abstract] [Full Text] [Related]

  • 57. Antenatal ultrasonic diagnosis of Meckel Gruber syndrome (a case report with review of literature).
    Vernekar JA, Mishra GK, Pinto RG, Bhandari M, Mishra M.
    Australas Radiol; 1991 May 02; 35(2):186-8. PubMed ID: 1930022
    [Abstract] [Full Text] [Related]

  • 58. Jarcho-Levin syndrome: prenatal diagnosis, perinatal care, and follow-up of siblings.
    Lawson ME, Share J, Benacerraf B, Krauss CM.
    J Perinatol; 1997 May 02; 17(5):407-9. PubMed ID: 9373850
    [Abstract] [Full Text] [Related]

  • 59. The Pena-Shokeir syndrome: report of five cases and further delineation of the syndrome.
    Chen H, Blumberg B, Immken L, Lachman R, Rightmire D, Fowler M, Bachman R, Beemer FA.
    Am J Med Genet; 1983 Oct 02; 16(2):213-24. PubMed ID: 6650566
    [Abstract] [Full Text] [Related]

  • 60. [Ultrasonic diagnosis of a hereditary multiple malformation syndrome: Meckel-Gruber syndrome or Carpenter-Hunter syndrome].
    Adjahoto EO, De Grandi P, Maillard-Brignon C, Pescia G.
    J Gynecol Obstet Biol Reprod (Paris); 1992 Oct 02; 21(8):928-33. PubMed ID: 1491139
    [Abstract] [Full Text] [Related]

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