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

85 related items for PubMed ID: 9018425

  • 21. Using three-dimensional ultrasound to detect craniosynostosis in a fetus with Pfeiffer syndrome.
    Benacerraf BR, Spiro R, Mitchell AG.
    Ultrasound Obstet Gynecol; 2000 Sep; 16(4):391-4. PubMed ID: 11169319
    [Abstract] [Full Text] [Related]

  • 22. The Saethre-Chotzen syndrome.
    Kreiborg S, Pruzansky S, Pashayan H.
    Teratology; 1972 Dec; 6(3):287-94. PubMed ID: 4643612
    [No Abstract] [Full Text] [Related]

  • 23. Pfeiffer Syndrome type 2--case report.
    Oyamada MK, Ferreira HS, Hoff M.
    Sao Paulo Med J; 2003 Jul 01; 121(4):176-9. PubMed ID: 14595512
    [Abstract] [Full Text] [Related]

  • 24. [Syndromes 2. Pfeiffer syndrome].
    Freihofer HP.
    Ned Tijdschr Tandheelkd; 1998 Jul 01; 105(7):245-6. PubMed ID: 11928428
    [Abstract] [Full Text] [Related]

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

  • 26. Cloverleaf skull associated with Pfeiffer syndrome: pathology and management.
    Kroczek RA, Mühlbauer W, Zimmermann I.
    Eur J Pediatr; 1986 Oct 01; 145(5):442-5. PubMed ID: 3792393
    [Abstract] [Full Text] [Related]

  • 27. The cloverleaf skull.
    Banna M, Omojola MF, Toi A, de Sa DJ.
    Br J Radiol; 1980 Jul 01; 53(631):730-2. PubMed ID: 7426902
    [No Abstract] [Full Text] [Related]

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

  • 29. Apert syndrome associated with increased fetal nuchal translucency.
    Aleem S, Howarth ES.
    Prenat Diagn; 2005 Nov 01; 25(11):1066-7. PubMed ID: 16302163
    [No Abstract] [Full Text] [Related]

  • 30. Sonographic findings with Pfeiffer syndrome.
    Hill LM, Grzybek PC.
    Prenat Diagn; 1994 Jan 01; 14(1):47-9. PubMed ID: 8183836
    [No Abstract] [Full Text] [Related]

  • 31. Using principal component analysis to describe the Apert skull deformity and simulate its correction.
    Pluijmers BI, Ponniah AJ, Ruff C, Dunaway D.
    J Plast Reconstr Aesthet Surg; 2012 Dec 01; 65(12):1750-2. PubMed ID: 22883348
    [No Abstract] [Full Text] [Related]

  • 32. Tracheal anomalies in Pfeiffer syndrome.
    Hockstein NG, McDonald-McGinn D, Zackai E, Bartlett S, Huff DS, Jacobs IN.
    Arch Otolaryngol Head Neck Surg; 2004 Nov 01; 130(11):1298-302. PubMed ID: 15545585
    [Abstract] [Full Text] [Related]

  • 33. Clinical observation: ocular abnormalities in a patient with Pfeiffer syndrome (acrocephalosyndactyly, type V).
    Van Dyke DC, Zackai EH, Diamond GR.
    J Clin Dysmorphol; 1983 Nov 01; 1(4):2-5. PubMed ID: 6432965
    [No Abstract] [Full Text] [Related]

  • 34. Dentofacial characteristics in Apert syndrome: a case report.
    Batra P, Duggal R, Parkash H.
    J Indian Soc Pedod Prev Dent; 2002 Sep 01; 20(3):118-23. PubMed ID: 12435011
    [Abstract] [Full Text] [Related]

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

  • 36. Application of the three-dimensional maximum mode in prenatal diagnosis of Apert syndrome.
    Esser T, Rogalla P, Bamberg C, Kalache KD.
    Am J Obstet Gynecol; 2005 Nov 01; 193(5):1743-5. PubMed ID: 16260220
    [Abstract] [Full Text] [Related]

  • 37. 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]

  • 38. [Anesthetic management of an infant girl with cloverleaf syndrome].
    Kudoh O, Hanzawa K, Iwata H, Iizuka H, Suzuki K, Kugimiya T.
    Masui; 2006 Oct 01; 55(10):1273-6. PubMed ID: 17051994
    [Abstract] [Full Text] [Related]

  • 39. Pfeiffer-type cardiocranial syndrome: a patient with features of this condition and with an unbalanced subtelomeric rearrangement involving chromosomes 1p and 17q.
    McCann E, Sweeney E, Sills J, May P, Smith S.
    Clin Dysmorphol; 2006 Apr 01; 15(2):81-4. PubMed ID: 16531733
    [Abstract] [Full Text] [Related]

  • 40. Genetic drift. Prying open the box.
    Marion RW.
    Am J Med Genet; 1996 May 17; 63(2):329-31. PubMed ID: 8725779
    [No Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 5.