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

178 related items for PubMed ID: 3777025

  • 21. [Hypoglossia-hypodactylia].
    Kim KC.
    Ryoikibetsu Shokogun Shirizu; 2001; (33):848. PubMed ID: 11462717
    [No Abstract] [Full Text] [Related]

  • 22. [Smith-Lemli-Opitz syndrome: evaluation of the correlations between individual traits as an approach to the study of heterogeneity].
    Nikonovich IuB, Kaurov BA, Lur'e IV.
    Tsitol Genet; 1987; 21(1):57-60. PubMed ID: 3564150
    [Abstract] [Full Text] [Related]

  • 23. Aglossia-adactylia syndrome.
    Nevin NC, Burrows D, Allen G, Kernohan DC.
    J Med Genet; 1975 Mar; 12(1):89-93. PubMed ID: 1121025
    [Abstract] [Full Text] [Related]

  • 24.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 25.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 26. Syndrome characterized by lingual malformation, polydactyly, tachypnea, and psychomotor retardation (Mohr syndrome).
    Gustavson KH, Kreuger A, Petersson PO.
    Clin Genet; 1971 Mar; 2(4):261-6. PubMed ID: 5146584
    [No Abstract] [Full Text] [Related]

  • 27. [Aglossia-adactylia with jejunal atresia].
    Bury F, Willekens H, de Waele P, Marchal G, Kerremans R, Eggermont E.
    Arch Fr Pediatr; 1977 Mar; 34(7):604-10. PubMed ID: 337922
    [Abstract] [Full Text] [Related]

  • 28.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 29. [Aglossia-adactylia syndrome with anterior bimaxillary synostosis].
    Bernard R, Giraud F, Lachard J, Garcin M, Gola R, Roux J, Thureau E.
    Pediatrie; 1971 Dec; 26(8):877-83. PubMed ID: 5138737
    [No Abstract] [Full Text] [Related]

  • 30. Collagen XI sequence variations in nonsyndromic cleft palate, Robin sequence and micrognathia.
    Melkoniemi M, Koillinen H, Männikkö M, Warman ML, Pihlajamaa T, Kääriäinen H, Rautio J, Hukki J, Stofko JA, Cisneros GJ, Krakow D, Cohn DH, Kere J, Ala-Kokko L.
    Eur J Hum Genet; 2003 Mar; 11(3):265-70. PubMed ID: 12673280
    [Abstract] [Full Text] [Related]

  • 31. [On the causal and morphological etiology of the Pierre Robin syndrome].
    Becker R, Palm D.
    Dtsch Zahnarztl Z; 1966 Nov 01; 21(11):1321-38. PubMed ID: 5223982
    [No Abstract] [Full Text] [Related]

  • 32. Midline field defects and Hirschsprung disease.
    Say B, Smith DP.
    Am J Med Genet; 1996 Jan 22; 61(3):293-4. PubMed ID: 8741878
    [No Abstract] [Full Text] [Related]

  • 33. New syndrome: a digito-reno-cerebral syndrome.
    Eronen M, Somer M, Gustafsson B, Holmberg C.
    Am J Med Genet; 1985 Oct 22; 22(2):281-5. PubMed ID: 4050858
    [No Abstract] [Full Text] [Related]

  • 34. The Greig cephalopolysyndactyly syndrome in a Canadian family.
    Chudley AE, Houston CS.
    Am J Med Genet; 1982 Nov 22; 13(3):269-76. PubMed ID: 6295159
    [No Abstract] [Full Text] [Related]

  • 35.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 36.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 37. Pierre Robin syndrome with hyperphalangism-clinodactylysm of the index finger: a possible new palato-digital syndrome.
    Silengo MC, Franceschini P, Cerutti A, Fabris C.
    Pediatr Radiol; 1977 Oct 28; 6(3):178-80. PubMed ID: 927984
    [Abstract] [Full Text] [Related]

  • 38.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 39. Ectrodactyly, ectodermal dysplasia and cleft lip syndrome.
    Yap HK, Lee BW, Tay JS, Wong HB.
    J Singapore Paediatr Soc; 1985 Oct 28; 27(3-4):215-7. PubMed ID: 3831606
    [No Abstract] [Full Text] [Related]

  • 40. [Mohr and Claussen's syndrome (author's transl)].
    Pfeiffer RA, Majewski F, Mannkopf H.
    Klin Padiatr; 1973 May 28; 185(3):224-9. PubMed ID: 4795577
    [No Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 9.