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Journal Abstract Search

598 related items for PubMed ID: 4997860

  • 1. Genetics of the Meckel syndrome (dysencephalia splanchnocystica).
    Hsia YE, Bratu M, Herbordt A.
    Pediatrics; 1971 Aug; 48(2):237-47. PubMed ID: 4997860
    [No Abstract] [Full Text] [Related]

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

  • 3. VACTERL with hydrocephalus: a further case with probable autosomal recessive inheritance.
    Corsello G, Giuffrè L.
    Am J Med Genet; 1994 Jan 01; 49(1):137-8. PubMed ID: 8172244
    [No Abstract] [Full Text] [Related]

  • 4. Meckel-Gruber syndrome.
    Ramachandran U, Malla T, Joshi KS.
    Kathmandu Univ Med J (KUMJ); 2006 Jan 01; 4(3):334-6. PubMed ID: 18603929
    [Abstract] [Full Text] [Related]

  • 5. [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]

  • 6. Familial holoprosencephaly.
    Dallaire L, Fraser FC, Wiglesworth FW.
    Birth Defects Orig Artic Ser; 1971 Jun 30; 7(7):136-42. PubMed ID: 5173201
    [Abstract] [Full Text] [Related]

  • 7. Polycystic kidneys associated with malformations of the brain, polydactyly, and other birth defects in newborn sibs. A lethal syndrome showing the autosomal-recessive pattern of inheritance.
    Fried K, Liban E, Lurie M, Friedman S, Reisner SH.
    J Med Genet; 1971 Sep 30; 8(3):285-90. PubMed ID: 4999589
    [No Abstract] [Full Text] [Related]

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  • 11. [Meckel syndrome in 2 brothers. Clinical, anatomopathologic and genetic aspects].
    Restrepo CM, García-Cruz D, Sánchez G, Cantú JM.
    Bol Med Hosp Infant Mex; 1988 Sep 30; 45(9):600-4. PubMed ID: 3190852
    [No Abstract] [Full Text] [Related]

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  • 13. The Meckel syndrome in Finland: epidemiologic and genetic aspects.
    Salonen R, Norio R.
    Am J Med Genet; 1984 Aug 30; 18(4):691-8. PubMed ID: 6486168
    [Abstract] [Full Text] [Related]

  • 14. Familial holoprosencephaly, heart defects, and polydactyly.
    Hennekam RC, van Noort G, de la Fuente AA.
    Am J Med Genet; 1991 Nov 01; 41(2):258-62. PubMed ID: 1785646
    [Abstract] [Full Text] [Related]

  • 15. 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 01; 14(2):97-103. PubMed ID: 4997715
    [No Abstract] [Full Text] [Related]

  • 16. [Tetrasomy 9p].
    Foerster W, Koch M, Hansen S.
    Monatsschr Kinderheilkd; 1985 Sep 01; 133(9):694-7. PubMed ID: 2865673
    [Abstract] [Full Text] [Related]

  • 17. A lethal syndrome of microcephaly with multiple congenital anomalies in three siblings.
    Neu RL, Kajii T, Gardner LI, Nagyfy SF.
    Pediatrics; 1971 Mar 01; 47(3):610-2. PubMed ID: 5547878
    [No Abstract] [Full Text] [Related]

  • 18. New manifestations in an infant with Neu Laxova syndrome.
    Rouzbahani L.
    Am J Med Genet; 1995 Mar 27; 56(2):239-40. PubMed ID: 7625453
    [No Abstract] [Full Text] [Related]

  • 19. Popliteal pterygium syndrome. Evidence for a severe autosomal recessive form.
    Bartsocas CS, Papas CV.
    J Med Genet; 1972 Jun 27; 9(2):222-6. PubMed ID: 4339984
    [No Abstract] [Full Text] [Related]

  • 20. Phenotypic variability in Meckel-Gruber syndrome.
    Farag TI, Usha R, Uma R, Mady SA, al-Nagdy K, el-Badramany MH.
    Clin Genet; 1990 Sep 27; 38(3):176-9. PubMed ID: 2225527
    [Abstract] [Full Text] [Related]

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