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Journal Abstract Search

130 related items for PubMed ID: 6486166

  • 21. An autosomal recessive mental retardation syndrome with hepatic fibrosis and renal cysts.
    Thompson E, Baraitser M.
    Am J Med Genet; 1986 May; 24(1):151-8. PubMed ID: 3085498
    [Abstract] [Full Text] [Related]

  • 22. Phenotypic variation in Meckel syndrome.
    Seller MJ.
    Clin Genet; 1981 Jul; 20(1):74-7. PubMed ID: 7296953
    [Abstract] [Full Text] [Related]

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

  • 24. Chromosomal abnormality (46,XX,3p plus) in a case of the Meckel syndrome.
    Hsia YE, Appadorai V, Breg WR, Howard RO.
    Birth Defects Orig Artic Ser; 1974 Sep; 10(8):19-25. PubMed ID: 4142400
    [No Abstract] [Full Text] [Related]

  • 25. Prenatal diagnosis of Meckel syndrome: alpha-feto protein and beta-trace protein in amniotic fluid.
    Chemke J, Miskin A, Rav-Acha Z, Porath A, Sagiv M, Katz Z.
    Clin Genet; 1977 Apr; 11(4):285-9. PubMed ID: 66999
    [Abstract] [Full Text] [Related]

  • 26. Relatively high prevalence of the Meckel syndrome among Jews.
    Fried K.
    Isr J Med Sci; 1973 Apr; 9(9):1399. PubMed ID: 4775123
    [No Abstract] [Full Text] [Related]

  • 27. Prenatal diagnosis of Meckel-Gruber syndrome and Dandy-Walker malformation in four consecutive affected siblings, with the fourth one being diagnosed prenatally at 22 weeks of gestation.
    Balci S, Tekşen F, Dökmeci F, Cengiz B, Cömert RB, Can B, Ozdamar S.
    Turk J Pediatr; 2004 Apr; 46(3):283-8. PubMed ID: 15503488
    [Abstract] [Full Text] [Related]

  • 28. Encephalocele, polycystic kidneys, and polydactyly with other defects. A necropsy case of Meckel syndrome and a review of literature.
    Ueda N, Sasaki N, Sugita A, Gotoh N, Yamamoto S, Yano T, Ochi H, Nishimura T, Matsuura S, Fukunishi R.
    Acta Pathol Jpn; 1987 Feb; 37(2):323-30. PubMed ID: 3604681
    [Abstract] [Full Text] [Related]

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

  • 30. Prenatal diagnosis of recurrent Meckel syndrome.
    Ramadani HM, Nasrat HA.
    Int J Gynaecol Obstet; 1992 Dec; 39(4):327-32. PubMed ID: 1361467
    [Abstract] [Full Text] [Related]

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

  • 32. Meckel Gruber syndrome--a single gene cause of recurrent neural tube defects.
    de Silva D, Suriyawansa D, Mangalika M, Samarasinghe D.
    Ceylon Med J; 2001 Mar; 46(1):30. PubMed ID: 11570001
    [Abstract] [Full Text] [Related]

  • 33. Visceral anomalies in the Meckel syndrome.
    Rapola J, Salonen R.
    Teratology; 1985 Apr; 31(2):193-201. PubMed ID: 3992488
    [Abstract] [Full Text] [Related]

  • 34. [Meckel-Gruber syndrome].
    Kondo I.
    Ryoikibetsu Shokogun Shirizu; 2000 Apr; (30 Pt 5):18-20. PubMed ID: 11057128
    [No Abstract] [Full Text] [Related]

  • 35. 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; 14(2):97-103. PubMed ID: 4997715
    [No Abstract] [Full Text] [Related]

  • 36. Are bowing of long tubular bones and preaxial polydactyly signs of the Meckel syndrome?
    Majewski F, Stöss H, Goecke T, Kemperdick H.
    Hum Genet; 1983 Jun; 65(2):125-33. PubMed ID: 6654326
    [Abstract] [Full Text] [Related]

  • 37. Ectrodactyly and absence (hypoplasia) of the tibia: are there dominant and recessive types?
    Majewski E, Goecke T, Meinecke P.
    Am J Med Genet; 1996 May 03; 63(1):185-9. PubMed ID: 8723107
    [Abstract] [Full Text] [Related]

  • 38. Three new cases of Tel Hashomer camptodactyly syndrome in one Arabic family.
    Tylki-Szymanska A.
    Am J Med Genet; 1986 Mar 03; 23(3):759-63. PubMed ID: 3953674
    [Abstract] [Full Text] [Related]

  • 39. Association of Meckel syndrome with M-anisosplenia in one patient.
    Moerman P, Verbeken E, Fryns JP, Goddeeris P, Lauweryns JM.
    Clin Genet; 1982 Sep 03; 22(3):143-7. PubMed ID: 7151299
    [No Abstract] [Full Text] [Related]

  • 40. [Meckel-Gruber syndrome].
    Henkel KE, Pfeiffer RA, Stöss H.
    Pathologe; 1993 Jan 03; 14(1):32-5. PubMed ID: 8451225
    [No Abstract] [Full Text] [Related]

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