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

169 related items for PubMed ID: 16259327

  • 1. Robinow Syndrome: a case report.
    Gulcan H, Akinci A, Aktar A.
    Genet Couns; 2005; 16(3):297-300. PubMed ID: 16259327
    [Abstract] [Full Text] [Related]

  • 2. [Robinow's syndrome associated with deafness].
    Samoud A, Menif K, Boulaares M, Ben Dridi MF.
    Arch Fr Pediatr; 1993 Dec; 50(10):897-9. PubMed ID: 8053771
    [Abstract] [Full Text] [Related]

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

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

  • 5. Robinow syndrome (Fetal Face syndrome).
    Menon PS, Thomas S, Mathews AR, Verma IC, Gupta A.
    Indian Pediatr; 1983 Oct; 20(10):783-7. PubMed ID: 6676283
    [No Abstract] [Full Text] [Related]

  • 6. Orofacial manifestations of Robinow's syndrome: a case report in a pediatric patient.
    Cerqueira DF, de Souza IP.
    Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2008 Mar; 105(3):353-7. PubMed ID: 18061493
    [Abstract] [Full Text] [Related]

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

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

  • 9. Is the frequency of Robinow syndrome relatively high in Turkey? Four more case reports.
    Akşit S, Aydinlioglu H, Dizdarer G, Caglayan S, Bektaşlar D, Cin A.
    Clin Genet; 1997 Oct; 52(4):226-30. PubMed ID: 9383028
    [Abstract] [Full Text] [Related]

  • 10. Ror2 knockout mouse as a model for the developmental pathology of autosomal recessive Robinow syndrome.
    Schwabe GC, Trepczik B, Süring K, Brieske N, Tucker AS, Sharpe PT, Minami Y, Mundlos S.
    Dev Dyn; 2004 Feb; 229(2):400-10. PubMed ID: 14745966
    [Abstract] [Full Text] [Related]

  • 11. Clinical characterization of autosomal dominant and recessive variants of Robinow syndrome.
    Mazzeu JF, Pardono E, Vianna-Morgante AM, Richieri-Costa A, Ae Kim C, Brunoni D, Martelli L, de Andrade CE, Colin G, Otto PA.
    Am J Med Genet A; 2007 Feb 15; 143(4):320-5. PubMed ID: 17256787
    [Abstract] [Full Text] [Related]

  • 12. Fryns syndrome with atypical findings--with large midline cleft on forehead but normal cranial MRI findings.
    Demirel G, Oguz SS, Celik IH, Yilmaz Y, Uras N, Erdeve O, Dilmen U.
    Genet Couns; 2010 Feb 15; 21(4):405-9. PubMed ID: 21290970
    [Abstract] [Full Text] [Related]

  • 13. Craniofacial phenotypes associated with Robinow syndrome.
    Conlon CJ, Abu-Ghname A, Raghuram AC, Davis MJ, Guillen DE, Sutton VR, Carvalho CMB, Maricevich RS.
    Am J Med Genet A; 2021 Dec 15; 185(12):3606-3612. PubMed ID: 33237614
    [Abstract] [Full Text] [Related]

  • 14. [Robinow syndrome].
    Kawame H.
    Ryoikibetsu Shokogun Shirizu; 2000 Dec 15; (30 Pt 5):236-7. PubMed ID: 11057211
    [No Abstract] [Full Text] [Related]

  • 15. Bartsocas-Papas syndrome in a Pakistani family from Kuwait.
    Al-Sawan RM, Soni AL, Al-Nakkas EM, Gang RK.
    Indian Pediatr; 2004 Jul 15; 41(7):725-7. PubMed ID: 15297688
    [Abstract] [Full Text] [Related]

  • 16. Congenital heart disease and Robinow syndrome.
    Atalay S, Ege B, Imamoğlu A, Suskan E, Ocal B, Gümüş H.
    Clin Dysmorphol; 1993 Jul 15; 2(3):208-10. PubMed ID: 8287182
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. Autosomal recessive Robinow syndrome: a case report.
    Grothe R, Anderson-Cermin C, Beiraghi S.
    J Dent Child (Chic); 2008 Jul 15; 75(1):48-54. PubMed ID: 18505648
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. Anaesthetic implications of the child with Robinow syndrome.
    Sleesman JB, Tobias JD.
    Paediatr Anaesth; 2003 Sep 15; 13(7):629-32. PubMed ID: 12950866
    [Abstract] [Full Text] [Related]

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