These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

231 related items for PubMed ID: 4999589

  • 21. 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; 93(6):483-91. PubMed ID: 5025032
    [No Abstract] [Full Text] [Related]

  • 22. Multiple congenital malformations in two sibs reminiscent of hydrolethalus and pseudotrisomy 13 syndromes.
    Dincsoy MY, Salih MA, al-Jurayyan N, al Saadi M, Patel PJ.
    Am J Med Genet; 1995 Apr 10; 56(3):317-21. PubMed ID: 7778599
    [Abstract] [Full Text] [Related]

  • 23. New autosomal recessive lethal disorder with polycystic kidneys type Potter I, characteristic face, microcephaly, brachymelia, and congenital heart defects.
    Gillessen-Kaesbach G, Meinecke P, Garrett C, Padberg BC, Rehder H, Passarge E.
    Am J Med Genet; 1993 Feb 15; 45(4):511-8. PubMed ID: 8465860
    [Abstract] [Full Text] [Related]

  • 24. New autosomal recessive faciodigitogenital syndrome.
    Teebi AS, Naguib KK, Al-Awadi S, Al-Saleh QA.
    J Med Genet; 1988 Jun 15; 25(6):400-6. PubMed ID: 3398008
    [Abstract] [Full Text] [Related]

  • 25. Polycystic kidney disease, biliary dysgenesis in a patient with Larsen's syndrome.
    Kurtoglu S, Dundar M, Hallaç IK, Uzüm K, Okumuş Y, Oktem T.
    Clin Genet; 1997 Jun 15; 51(6):408-11. PubMed ID: 9237505
    [Abstract] [Full Text] [Related]

  • 26. Meckel-Gruber syndrome. A lethal combination of abnormalities.
    Coard KC, Escoffery CT.
    West Indian Med J; 1990 Mar 15; 39(1):52-6. PubMed ID: 2333699
    [Abstract] [Full Text] [Related]

  • 27.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 28. The Roberts syndrome.
    Freeman MV, Williams DW, Schimke RN, Temtamy SA, Vachier E, German J.
    Birth Defects Orig Artic Ser; 1974 Mar 15; 10(5):87-95. PubMed ID: 4220010
    [Abstract] [Full Text] [Related]

  • 29.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 30.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 31.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 32. [The oro-facial-digital syndrome. Symptoms and prognosis].
    Majewski F, Lenz W, Pfeiffer RA, Tünte W, Müller H.
    Z Kinderheilkd; 1972 Mar 15; 112(1):89-112. PubMed ID: 4336265
    [No Abstract] [Full Text] [Related]

  • 33. Dandy-Walker malformation in the Meckel syndrome.
    Summers MC, Donnenfeld AE.
    Am J Med Genet; 1995 Jan 02; 55(1):57-61. PubMed ID: 7702098
    [Abstract] [Full Text] [Related]

  • 34. The adducted thumbs syndrome. An autosomal recessive disease with arthrogryposis, dysmyelination, craniostenosis, and cleft palate.
    Christian JC, Andrews PA, Conneally PM, Muller J.
    Clin Genet; 1971 Jan 02; 2(2):95-103. PubMed ID: 5116596
    [No Abstract] [Full Text] [Related]

  • 35. Gross anatomical studies of a newborn with the Meckel syndrome.
    Pettersen JC.
    Teratology; 1983 Oct 02; 28(2):157-64. PubMed ID: 6648819
    [Abstract] [Full Text] [Related]

  • 36. Visceral anomalies in the Meckel syndrome.
    Rapola J, Salonen R.
    Teratology; 1985 Apr 02; 31(2):193-201. PubMed ID: 3992488
    [Abstract] [Full Text] [Related]

  • 37. Fetal autopsy of Meckel Gruber syndrome -a case report.
    Bolineni C, Nagamuthu EA, Neelala N.
    Fetal Pediatr Pathol; 2013 Oct 02; 32(5):387-93. PubMed ID: 23445452
    [Abstract] [Full Text] [Related]

  • 38. [Polycystic disease with recessive transmission].
    Martini A.
    Minerva Urol Nefrol; 1987 Oct 02; 39(3):259-62. PubMed ID: 3438795
    [No Abstract] [Full Text] [Related]

  • 39. Early prenatal diagnosis of Meckel syndrome--a case report.
    Yu CJ, Chen CP, Jeng CJ, Yang YC.
    Zhonghua Yi Xue Za Zhi (Taipei); 1990 Jul 02; 46(1):53-6. PubMed ID: 2176925
    [Abstract] [Full Text] [Related]

  • 40. The Meckel syndrome in Finland: epidemiologic and genetic aspects.
    Salonen R, Norio R.
    Am J Med Genet; 1984 Aug 02; 18(4):691-8. PubMed ID: 6486168
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 12.