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Journal Abstract Search

337 related items for PubMed ID: 7442848

  • 21. [Meckel syndrome (author's transl)].
    Alonso JA, Gómez Castillo E, Arribas M, Luque R, Rubio C.
    An Esp Pediatr; 1979 May; 12(5):403-10. PubMed ID: 464411
    [Abstract] [Full Text] [Related]

  • 22. DNA marker analysis of adult polycystic kidney disease in Italian families. Italian Cooperative Group on ADPKD.
    Potenza L, Mandich P, Restagno G, Bellone E, Novelli G, Dallapiccola B, Ajmar F, Carbonara A.
    Prog Clin Biol Res; 1989 May; 305():77-81. PubMed ID: 2569744
    [No Abstract] [Full Text] [Related]

  • 23. 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 May; 34(2):73-81. PubMed ID: 7336916
    [No Abstract] [Full Text] [Related]

  • 24. [Congenital malformations--multiple abnormalities syndromes].
    le Merrer M.
    Soins Gynecol Obstet Pueric Pediatr; 1990 Mar; (106):15-9. PubMed ID: 2193410
    [No Abstract] [Full Text] [Related]

  • 25. Survival and spectrum of anomalies in the Meckel syndrome.
    Lowry RB, Hill RH, Tischler B.
    Am J Med Genet; 1983 Mar; 14(3):417-21. PubMed ID: 6859092
    [Abstract] [Full Text] [Related]

  • 26. Goldston syndrome: report of a case.
    Gulcan YH, Duman N, Kumral A, Sağol, Lebe B, Kavukçu S, Erçal D, Celiloğlu M, Ozkan H.
    Genet Couns; 2001 Mar; 12(3):263-7. PubMed ID: 11693790
    [Abstract] [Full Text] [Related]

  • 27. Genetics, pathoanatomy and prenatal diagnosis of Potter I syndrome and other urogenital tract diseases.
    Schmidt W, Schroeder TM, Buchinger G, Kubli F.
    Clin Genet; 1982 Sep; 22(3):105-27. PubMed ID: 7151297
    [Abstract] [Full Text] [Related]

  • 28. [Familial occurrence of bilateral renal agenesis].
    Kovács T, Csécsei K, Tóth Z, Papp Z.
    Orv Hetil; 1990 Jan 21; 131(3):133-5. PubMed ID: 2300395
    [Abstract] [Full Text] [Related]

  • 29. Autosomal dominant polycystic kidney disease diagnosed in utero using ultrasonography.
    Smedley MG, Bailey RR.
    N Z Med J; 1987 Sep 23; 100(832):606. PubMed ID: 3330592
    [No Abstract] [Full Text] [Related]

  • 30. Gross anatomical studies of a newborn infant with the Meckel syndrome.
    Pettersen JC.
    Am J Med Genet; 1984 Aug 23; 18(4):649-59. PubMed ID: 6486165
    [Abstract] [Full Text] [Related]

  • 31. Ultrasonographic parameters in the prenatal diagnosis of Meckel syndrome.
    Wapner RJ, Kurtz AB, Ross RD, Jackson LG.
    Obstet Gynecol; 1981 Mar 23; 57(3):388-92. PubMed ID: 7465155
    [Abstract] [Full Text] [Related]

  • 32. [2 new cases of Meckel-Gruber syndrome in the same family].
    Franzoni R, Scalercio A.
    Minerva Pediatr; 1986 Sep 30; 38(17-18):783-9. PubMed ID: 3796537
    [No Abstract] [Full Text] [Related]

  • 33. Genetic counseling in adult polycystic kidney disease.
    Sahney S, Weiss L, Levin NW.
    Am J Med Genet; 1982 Apr 30; 11(4):461-8. PubMed ID: 7091189
    [Abstract] [Full Text] [Related]

  • 34. [Prenatal diagnosis of Meckel-Gruber's syndrome by ultrasound (author's transl(].
    Schmidt W, von Holst T, Schroeder T, Kubli F.
    Z Geburtshilfe Perinatol; 1981 Feb 30; 185(1):67-71. PubMed ID: 7195120
    [Abstract] [Full Text] [Related]

  • 35. Familial renal dysplasia. Microdissection studies in siblings with associated central nervous system and hepatic malformations.
    Miranda D, Schinella RA, Finegold MJ.
    Arch Pathol; 1972 Jun 30; 93(6):483-91. PubMed ID: 5025032
    [No Abstract] [Full Text] [Related]

  • 36. [Age at diagnosis of adult renal polycystosis. A health problem].
    Ortega F, Tenorio R, Torres A, Marín R, Gago E, Alvarez Grande J.
    Rev Clin Esp; 1983 Jan 31; 168(2):105-8. PubMed ID: 6856895
    [No Abstract] [Full Text] [Related]

  • 37. [Connatal cystic kidneys].
    Schwesinger G, Gätke U.
    Padiatr Grenzgeb; 1985 Jan 31; 24(3):221-7. PubMed ID: 4011279
    [No Abstract] [Full Text] [Related]

  • 38. [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]

  • 39. Polydactyly in a carrier of the gene for the Meckel syndrome.
    Nelson J, Nevin NC, Hanna EJ.
    Am J Med Genet; 1994 Nov 15; 53(3):207-9. PubMed ID: 7856653
    [Abstract] [Full Text] [Related]

  • 40. A high incidence of PKD in a large geographic area of south-western Hungary: a medical genetic study.
    Forrai G, Tauszik T, Tauszik N, Mohr T, Tunyogi MC, Holics C, Bánkövi G, Gál I.
    Prog Clin Biol Res; 1989 Nov 15; 305():89-94. PubMed ID: 2762359
    [No Abstract] [Full Text] [Related]

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