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

297 related items for PubMed ID: 11183188

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 23.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

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

  • 26. An epidemiological study of Wolf-Hirschhorn syndrome: life expectancy and cause of mortality.
    Shannon NL, Maltby EL, Rigby AS, Quarrell OW.
    J Med Genet; 2001 Oct; 38(10):674-9. PubMed ID: 11584045
    [Abstract] [Full Text] [Related]

  • 27.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 29.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 30. Chromosome healing of constitutional chromosome deletions studied by microdissection.
    Vermeesch JR, Falzetti D, Van Buggenhout G, Fryns JP, Marynen P.
    Cytogenet Cell Genet; 1998 Oct; 81(1):68-72. PubMed ID: 9691179
    [Abstract] [Full Text] [Related]

  • 31. Ring chromosome 4 in a patient with early onset type 2 diabetes, deafness, and developmental delay.
    Blackett PR, Li S, Mulvihill JJ.
    Am J Med Genet A; 2005 Aug 30; 137(2):213-6. PubMed ID: 16082703
    [Abstract] [Full Text] [Related]

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

  • 33. [Paternally originated Wolf-Hirschhorn syndrome detected by multiplex ligation-dependent probe amplification and microarray comparative genomic hybridization].
    Zhu CJ, Huang ZY, Wu WQ, Zhao Q, Jiang HY, Xie JS.
    Zhonghua Er Ke Za Zhi; 2012 Jun 30; 50(6):460-4. PubMed ID: 22931946
    [Abstract] [Full Text] [Related]

  • 34. The new Wolf-Hirschhorn syndrome critical region (WHSCR-2): a description of a second case.
    Rodríguez L, Zollino M, Climent S, Mansilla E, López-Grondona F, Martínez-Fernández ML, Murdolo M, Martínez-Frías ML.
    Am J Med Genet A; 2005 Jul 15; 136(2):175-8. PubMed ID: 15948183
    [Abstract] [Full Text] [Related]

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

  • 36. A submicroscopic translocation, t(4;10), responsible for recurrent Wolf-Hirschhorn syndrome identified by allele loss and fluorescent in situ hybridisation.
    Goodship J, Curtis A, Cross I, Brown J, Emslie J, Wolstenholme J, Bhattacharya S, Burn J.
    J Med Genet; 1992 Jul 15; 29(7):451-4. PubMed ID: 1640422
    [Abstract] [Full Text] [Related]

  • 37. Wolf-Hirschhorn Syndrome with Epibulbar Dermoid: An Unusual Association in a Patient with 4p Deletion and Functional Xp Disomy.
    Bragagnolo S, Colovati ME, Guilherme RS, Dantas AG, de Souza MZ, de Soares MF, Melaragno MI, Perez AB.
    Cytogenet Genome Res; 2016 Jul 15; 150(1):17-22. PubMed ID: 27842301
    [Abstract] [Full Text] [Related]

  • 38.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 39. Molecular characterisation of chromosome 4p deletions resulting in Wolf-Hirschhorn syndrome.
    Estabrooks LL, Lamb AN, Aylsworth AS, Callanan NP, Rao KW.
    J Med Genet; 1994 Feb 15; 31(2):103-7. PubMed ID: 8182713
    [Abstract] [Full Text] [Related]

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

    Page: [Previous] [Next] [New Search]
    of 15.