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

131 related items for PubMed ID: 24300290

  • 21. Spondylometaphyseal dysplasia, Sedaghatian type.
    Peeden JN, Rimoin DL, Lachman RS, Dyer ML, Gerard D, Gruber HE.
    Am J Med Genet; 1992 Nov 15; 44(5):651-6. PubMed ID: 1481828
    [Abstract] [Full Text] [Related]

  • 22. Mowat-Wilson syndrome associated with craniosynostosis.
    Hartill VL, Pendlebury M, Hobson E.
    Clin Dysmorphol; 2014 Jan 15; 23(1):16-19. PubMed ID: 24300291
    [No Abstract] [Full Text] [Related]

  • 23. Craniosynostosis and lid anomalies: report of a girl with Michels syndrome.
    Cunniff C, Jones KL.
    Am J Med Genet; 1990 Sep 15; 37(1):28-30. PubMed ID: 2240039
    [Abstract] [Full Text] [Related]

  • 24. Spondyloepiphyseal dysplasia, Omani type: further definition of the phenotype.
    van Roij MH, Mizumoto S, Yamada S, Morgan T, Tan-Sindhunata MB, Meijers-Heijboer H, Verbeke JI, Markie D, Sugahara K, Robertson SP.
    Am J Med Genet A; 2008 Sep 15; 146A(18):2376-84. PubMed ID: 18698629
    [Abstract] [Full Text] [Related]

  • 25. Craniosynostosis in cherubism.
    Stiller M, Urban M, Golder W, Tiziani V, Reichenberger E, Frege J, Opitz C, Peters H.
    Am J Med Genet; 2000 Dec 11; 95(4):325-31. PubMed ID: 11186885
    [Abstract] [Full Text] [Related]

  • 26. [Classification of craniosynostosis].
    Renier D, Arnaud E, Marchac D.
    Neurochirurgie; 2006 Jun 11; 52(2-3 Pt 2):200-27. PubMed ID: 16981654
    [No Abstract] [Full Text] [Related]

  • 27. Craniosynostosis associated with ectopia lentis in monozygotic twin sisters.
    Cruysberg JR, van Ravenswaaij-Arts CM, Pinckers A, Roddi R, Brunner HG.
    Am J Med Genet; 1999 Jan 29; 82(3):201-5. PubMed ID: 10215540
    [Abstract] [Full Text] [Related]

  • 28. Craniosynostosis associated with intracranial calcification: a novel recessive syndrome.
    Longman C, Whiteford M, Koppel D, Donaldson M, Paterson W, Tolmie J.
    Clin Dysmorphol; 2003 Oct 29; 12(4):215-20. PubMed ID: 14564206
    [Abstract] [Full Text] [Related]

  • 29. The evolving craniofacial phenotype of a patient with Sensenbrenner syndrome caused by IFT140 compound heterozygous mutations.
    Bayat A, Kerr B, Douzgou S, DDD Study.
    Clin Dysmorphol; 2017 Oct 29; 26(4):247-251. PubMed ID: 28288023
    [No Abstract] [Full Text] [Related]

  • 30. Normal growth and development in a child with Baller-Gerold syndrome (craniosynostosis and radial aplasia).
    Galea P, Tolmie JL.
    J Med Genet; 1990 Dec 29; 27(12):784-7. PubMed ID: 2074565
    [Abstract] [Full Text] [Related]

  • 31. Severe Aortic Root Dilatation in a Patient With Larsen Syndrome.
    Eletta R, Pandey A, Dharmasaputra T, Moreno M, Oparaugo Y, Kumar TS, Beker S.
    World J Pediatr Congenit Heart Surg; 2023 Jul 29; 14(4):532-535. PubMed ID: 37410597
    [Abstract] [Full Text] [Related]

  • 32.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 33. Obesity, hypothyroidism, craniosynostosis, cardiac hypertrophy, colitis, and developmental delay: a novel syndrome.
    Tan TY, Amor DJ.
    Am J Med Genet A; 2007 Jan 15; 143A(2):114-8. PubMed ID: 17163533
    [Abstract] [Full Text] [Related]

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

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

  • 36. A lethal skeletal dysplasia with generalised sclerosis and advanced skeletal maturation: Blomstrand chondrodysplasia?
    Young ID, Zuccollo JM, Broderick NJ.
    J Med Genet; 1993 Feb 15; 30(2):155-7. PubMed ID: 8445622
    [Abstract] [Full Text] [Related]

  • 37. Spondylometaphyseal dysplasia with cone-rod dystrophy.
    Walters BA, Raff ML, Hoeve JV, Tesser R, Langer LO, France TD, Glass IA, Pauli RM.
    Am J Med Genet A; 2004 Sep 01; 129A(3):265-76. PubMed ID: 15326626
    [Abstract] [Full Text] [Related]

  • 38. Phenotypic diversity in patients with craniosynostoses unrelated to Apert syndrome: the role of fibroblast growth factor receptor gene mutations.
    Ito S, Sekido K, Kanno H, Sato H, Tanaka M, Yamaguchi K, Yamamoto I.
    J Neurosurg; 2005 Jan 01; 102(1 Suppl):23-30. PubMed ID: 16206730
    [Abstract] [Full Text] [Related]

  • 39. Further delineation of the Baller-Gerold syndrome.
    Lin AE, McPherson E, Nwokoro NA, Clemens M, Losken HW, Mulvihill JJ.
    Am J Med Genet; 1993 Feb 15; 45(4):519-24. PubMed ID: 8465861
    [Abstract] [Full Text] [Related]

  • 40. Evolution of the phenotype of craniosynostosis with dental anomalies syndrome and report of IL11RA variant population frequencies in a Crouzon-like autosomal recessive syndrome.
    Korakavi N, Prokop JW, Seaver LH.
    Am J Med Genet A; 2019 Apr 15; 179(4):668-673. PubMed ID: 30811827
    [Abstract] [Full Text] [Related]

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