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Journal Abstract Search

193 related items for PubMed ID: 7205201

  • 61.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 62. Prenatal diagnosis of Meckel Gruber syndrome presenting with renal agenesis: report of a case.
    Guven MA, Ceylaner S, Ceylaner G, Gul D, Ertas IE.
    Genet Couns; 2006; 17(1):65-8. PubMed ID: 16719279
    [No Abstract] [Full Text] [Related]

  • 63. Meckel syndrome: prenatal ultrasonographic diagnosis in two cases showing marked differences in phenotypic expression.
    Gallimore AP, Davies PF.
    Australas Radiol; 1992 Feb; 36(1):62-4. PubMed ID: 1632751
    [Abstract] [Full Text] [Related]

  • 64. Meckel Gruber syndrome, A case report.
    Aslan K, Külahçı Aslan E, Orhan A, Atalay MA.
    Organogenesis; 2015 Feb; 11(2):87-92. PubMed ID: 26037304
    [Abstract] [Full Text] [Related]

  • 65. Fibrosis of the liver in Meckel Gruber syndrome.
    de Silva MV, Senanayake HM.
    Indian Pediatr; 2001 Nov; 38(11):1325-7. PubMed ID: 11721082
    [No Abstract] [Full Text] [Related]

  • 66. Retrospective diagnosis and subsequent prenatal diagnosis of Nijmegen breakage syndrome.
    Muschke P, Gola H, Varon R, Röpke A, Zumkeller W, Wieacker P, Stumm M.
    Prenat Diagn; 2004 Feb; 24(2):111-3. PubMed ID: 14974117
    [Abstract] [Full Text] [Related]

  • 67. Diagnosis of the Meckel-Gruber syndrome at eleven to fourteen weeks' gestation.
    Sepulveda W, Sebire NJ, Souka A, Snijders RJ, Nicolaides KH.
    Am J Obstet Gynecol; 1997 Feb; 176(2):316-9. PubMed ID: 9065174
    [Abstract] [Full Text] [Related]

  • 68.
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  • 69. [Meckel syndrome: prenatal diagnosis and pathology].
    Csécsei K, Szeifert G, Tóth Z, Szabó M, Pap G, Tankó A, Papp Z.
    Orv Hetil; 1986 Feb 16; 127(7):395-8. PubMed ID: 3951857
    [No Abstract] [Full Text] [Related]

  • 70. Cri du chat and Potter syndromes: a decision to abort.
    David A, Desai N, Udvardy M, High D, Engelberg J.
    Hosp Pract (Off Ed); 1992 Sep 15; 27(9):197-200, 204-6. PubMed ID: 1522159
    [No Abstract] [Full Text] [Related]

  • 71.
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  • 72. Prenatal diagnosis of occipital encephalocele, mega-cisterna magna, mesomelic shortening, and clubfeet associated with pure tetrasomy 20p.
    Wu YC, Fang JS, Lee KF, Estipona J, Yang ML, Yuan CC.
    Prenat Diagn; 2003 Feb 15; 23(2):124-7. PubMed ID: 12575018
    [Abstract] [Full Text] [Related]

  • 73. Association of Meckel syndrome with M-anisosplenia in one patient.
    Moerman P, Verbeken E, Fryns JP, Goddeeris P, Lauweryns JM.
    Clin Genet; 1982 Sep 15; 22(3):143-7. PubMed ID: 7151299
    [No Abstract] [Full Text] [Related]

  • 74. [A familial case of oral-facial-digital syndrome].
    Sakata M, Ohshige T, Yamaguchi M, Mori N, Miyakawa I.
    Nihon Sanka Fujinka Gakkai Zasshi; 1990 Nov 15; 42(11):1587-90. PubMed ID: 2273318
    [No Abstract] [Full Text] [Related]

  • 75. Major congenital malformations in 5448 newborns: comments on genetic counseling and prenatal diagnosis.
    Van Regemorter N, Dodion J, Druart C, Hayez F, Vamos E, Rodesch F.
    Acta Paediatr Belg; 1981 Nov 15; 34(2):73-81. PubMed ID: 7336916
    [No Abstract] [Full Text] [Related]

  • 76. Amniotic fluid pregnancy-specific beta 1-glycoprotein (SP1) in Meckel's syndrome: a new test for prenatal diagnosis?
    Heikinheimo M, Aula P, Rapola J, Wahlström T, Jalanko H, Seppälä M.
    Prenat Diagn; 1982 Apr 15; 2(2):103-8. PubMed ID: 6183654
    [No Abstract] [Full Text] [Related]

  • 77.
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  • 78. Genetic heterogeneity of Meckel syndrome.
    Roume J, Ma HW, Le Merrer M, Cormier-Daire V, Girlich D, Genin E, Munnich A.
    J Med Genet; 1997 Dec 15; 34(12):1003-6. PubMed ID: 9429143
    [Abstract] [Full Text] [Related]

  • 79.
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  • 80.
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