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

138 related items for PubMed ID: 4837288

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

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. Arthrogryposis multiplex congenita: twenty-three cases in an Arab kindred.
    Lebenthal E, Shochet SB, Adam A, Seelenfreund M, Fried A, Najenson T, Sandbank U, Matoth Y.
    Pediatrics; 1970 Dec; 46(6):891-9. PubMed ID: 5491443
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. Identification of a novel CNTNAP1 mutation causing arthrogryposis multiplex congenita with cerebral and cerebellar atrophy.
    Lakhani S, Doan R, Almureikhi M, Partlow JN, Al Saffar M, Elsaid MF, Alaaraj N, James Barkovich A, Walsh CA, Ben-Omran T.
    Eur J Med Genet; 2017 May; 60(5):245-249. PubMed ID: 28254648
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. Family studies for the mode of inheritance in arthrogryposis multiplex congenita.
    Bhatnagar DP, Sidhu LS, Aggarwal ND.
    Z Morphol Anthropol; 1977 Jul; 68(2):233-40. PubMed ID: 930240
    [No Abstract] [Full Text] [Related]

  • 13. Characterization of a group unrelated patients with arthrogryposis multiplex congenita.
    Valdés-Flores M, Casas-Avila L, Hernández-Zamora E, Kofman S, Hidalgo-Bravo A.
    J Pediatr (Rio J); 2016 Jul; 92(1):58-64. PubMed ID: 26453511
    [Abstract] [Full Text] [Related]

  • 14. Arthrogryposis, renal dysfunction and cholestasis syndrome.
    Abdullah MA, Al-Hasnan Z, Okamoto E, Abomelha AM.
    Saudi Med J; 2000 Mar; 21(3):297-9. PubMed ID: 11533803
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. Familial autosomal recessive rigid spine syndrome with neurogenic facio-scapulo-peroneal muscle atrophy.
    Palmucci L, Mongini T, Doriguzzi C, Maniscalco M, Schiffer D.
    J Neurol Neurosurg Psychiatry; 1991 Jan; 54(1):42-5. PubMed ID: 2010758
    [Abstract] [Full Text] [Related]

  • 17. Arthrogryposis, cholestatic pigmentary liver disease and renal dysfunction: report of a second family.
    Di Rocco M, Reboa E, Barabino A, Larnaout A, Canepa M, Savioli C, Cremonte M, Borrone C.
    Am J Med Genet; 1990 Oct; 37(2):237-40. PubMed ID: 2248291
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. Recessive mutations in SCYL2 cause a novel syndromic form of arthrogryposis in humans.
    Seidahmed MZ, Al-Kindi A, Alsaif HS, Miqdad A, Alabbad N, Alfifi A, Abdelbasit OB, Alhussein K, Alsamadi A, Ibrahim N, Al-Futaisi A, Al-Maawali A, Alkuraya FS.
    Hum Genet; 2020 Apr; 139(4):513-519. PubMed ID: 31960134
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 7.