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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

266 related items for PubMed ID: 4805907

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. M--craniocarpotarsal dystrophy (whistling face syndrome) in two families.
    Jorgenson RJ.
    Birth Defects Orig Artic Ser; 1974; 10(5):237-42. PubMed ID: 4220006
    [No Abstract] [Full Text] [Related]

  • 3.
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  • 4. [The Rubinstein-Taybi syndrome. A contribution to the problem of the period of determination].
    Grävinghoff J, Tost M.
    Monatsschr Kinderheilkd (1902); 1970 Aug; 118(8):479-84. PubMed ID: 5511841
    [No Abstract] [Full Text] [Related]

  • 5. Ocular hypertelorism and nasal agenesis (midface syndrome) with limb anomalies.
    Calli LJ.
    Birth Defects Orig Artic Ser; 1971 Jun; 7(7):268. PubMed ID: 5173220
    [No Abstract] [Full Text] [Related]

  • 6. Median cleft face syndrome associated with orbital hypertelorism and polysyndactyly.
    Ide CH, Holt JE.
    Eye Ear Nose Throat Mon; 1975 Apr; 54(4):150-1. PubMed ID: 164373
    [No Abstract] [Full Text] [Related]

  • 7. The Greig cephalopolysyndactyly syndrome in a Canadian family.
    Chudley AE, Houston CS.
    Am J Med Genet; 1982 Nov; 13(3):269-76. PubMed ID: 6295159
    [No Abstract] [Full Text] [Related]

  • 8. [Three new cases of Meckel's syndrome or Gruber's splanchnocystic dysencephaly in siblings. Anatomo-pathologic and cytogenetic study. Nosologic discussion].
    Naffah J, Ghosn G, Gharios N.
    Arch Fr Pediatr; 1972 Dec; 29(10):1069-81. PubMed ID: 4662280
    [No Abstract] [Full Text] [Related]

  • 9. Aarskog's syndrome.
    Maxwell GM.
    Med J Aust; 1982 Jul 24; 2(2):66-7. PubMed ID: 7121364
    [No Abstract] [Full Text] [Related]

  • 10. Undescribed combination of ocular (hypotelorism, optic disc anomaly, microcornea, exotropia), facial, auricular, phonic and other anomalies.
    Awan KJ.
    J Pediatr Ophthalmol; 1976 May 24; 13(3):149-55. PubMed ID: 828200
    [No Abstract] [Full Text] [Related]

  • 11. [Cardiovascular changes in the leopard syndrome].
    Januś S, Rudziński A, Popczyńska-Markowa M.
    Pol Tyg Lek; 1977 May 02; 32(18):687-9. PubMed ID: 866252
    [No Abstract] [Full Text] [Related]

  • 12. [Noonan's syndrome. Genetic and cardiological study of 2 cases].
    Saint-Rome G, Davignon A, Kratz C.
    Union Med Can; 1970 Sep 02; 99(9):1602-12. PubMed ID: 5005748
    [No Abstract] [Full Text] [Related]

  • 13. Megalocornea and mental retardation syndrome.
    Raas-Rothschild A, Berkenstadt M, Goodman RM.
    Am J Med Genet; 1988 Jan 02; 29(1):221-3. PubMed ID: 3344772
    [No Abstract] [Full Text] [Related]

  • 14. Yunis-Varon syndrome.
    Bhatia S, Holla RG.
    Indian Pediatr; 2005 Apr 02; 42(4):373-5. PubMed ID: 15876600
    [Abstract] [Full Text] [Related]

  • 15.
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  • 16. [Crouzon's craniofacial dysostosis with digital anomalies. Casuistic contribution].
    Manns KJ, Bopp KP.
    Med Klin; 1965 Nov 19; 60(47):1899-903. PubMed ID: 5882911
    [No Abstract] [Full Text] [Related]

  • 17. Rubinstein-Taybi syndrome.
    Gellis SS, Feingold M.
    Am J Dis Child; 1971 Apr 19; 121(4):327-8. PubMed ID: 5550739
    [No Abstract] [Full Text] [Related]

  • 18. The genetics of hand malformations.
    Temtamy SA, McKusick VA.
    Birth Defects Orig Artic Ser; 1978 Apr 19; 14(3):i-xviii, 1-619. PubMed ID: 215242
    [No Abstract] [Full Text] [Related]

  • 19. Ocular abnormalities in the median cleft face syndrome.
    Kinsey JA, Streeten BW.
    Am J Ophthalmol; 1977 Feb 19; 83(2):261-6. PubMed ID: 402078
    [Abstract] [Full Text] [Related]

  • 20.
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