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

156 related items for PubMed ID: 7521121

  • 21. GAPO syndrome: first Egyptian case with ultrastructural changes in the gingiva.
    Meguid NA, Afifi HH, Ramzy MI, Hindawy A, Temtamy SA.
    Clin Genet; 1997 Aug; 52(2):110-5. PubMed ID: 9298746
    [Abstract] [Full Text] [Related]

  • 22. GAPO syndrome: a novel variant in ANTXR1 gene.
    Damagatla M, Verma A, Pochaboina V, Bhate M, Senthil S.
    Ophthalmic Genet; 2024 Aug; 45(4):395-400. PubMed ID: 38691016
    [Abstract] [Full Text] [Related]

  • 23. GAPO syndrome in seven new patients: Identification of five novel ANTXR1 mutations including the first large intragenic deletion.
    Abdel-Hamid MS, Ismail S, Zaki MS, Abdel-Salam GMH, Otaify GA, Issa MY, Abdel-Kader M, Girgis M, Aboul-Ezz E, Mazen I, Aglan MS, Temtamy SA.
    Am J Med Genet A; 2019 Feb; 179(2):237-242. PubMed ID: 30575274
    [Abstract] [Full Text] [Related]

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

  • 25. Pseudoanodontia, cranial deformity, blindness, alopecia, and dwarfism: a new syndrome.
    Fuks A, Rosenmann A, Chosack A.
    ASDC J Dent Child; 1978 Feb; 45(2):155-7. PubMed ID: 350923
    [No Abstract] [Full Text] [Related]

  • 26.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 27. GAPO syndrome: three new Brazilian cases, additional osseous manifestations, and review of the literature.
    Goloni-Bertollo EM, Ruiz MT, Goloni CB, Muniz MP, Valério NI, Pavarino-Bertelli EC.
    Am J Med Genet A; 2008 Jun 15; 146A(12):1523-9. PubMed ID: 18470892
    [Abstract] [Full Text] [Related]

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

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 34.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 35. [The Robinow syndrome: a report of a family with autosomal dominant transmission].
    Díaz López MT, Lorenzo Sanz G, Quintana Castilla A, Esteve de Pablo C, Aparicio Meix JM.
    An Esp Pediatr; 1996 May 15; 44(5):520-3. PubMed ID: 8928981
    [No Abstract] [Full Text] [Related]

  • 36. [Intra uterine major dwarfism with dysmorphia and severe encephalopathy. Bird head dwarfism (Virchow-Seckel type)].
    Toudic L, Roche J, Alix D, Le Bars C, Dantoine G, Castel Y.
    Ann Pediatr (Paris); 1977 Oct 15; 24(10):653-6. PubMed ID: 16211901
    [No Abstract] [Full Text] [Related]

  • 37.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 38. Long-term follow-up and molecular characterization of a patient with a RECQL4 mutation spectrum disorder.
    Fradin M, Merklen-Djafri C, Perrigouard C, Aral B, Muller J, Stoetzel C, Frouin E, Flori E, Doray B, Dollfus H, Lipsker D.
    Dermatology; 2013 Oct 15; 226(4):353-7. PubMed ID: 23899764
    [Abstract] [Full Text] [Related]

  • 39.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 40.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 8.