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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

125 related items for PubMed ID: 21344639

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  • 2. Familial deletion of the HOXA gene cluster associated with Hand-Foot-Genital syndrome and phenotypic variability.
    Tas E, Sebastian J, Madan-Khetarpal S, Sweet P, Yatsenko AN, Pollock N, Rajkovic A, Schneck FX, Yatsenko SA, Witchel SF.
    Am J Med Genet A; 2017 Jan; 173(1):221-224. PubMed ID: 27649277
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  • 4. Deletion involving the TWIST locus and the HOXA cluster: a contiguous gene syndrome on 7p?
    Kosaki R, Higuchi M, Mitsui N, Matsushima K, Ohashi H, Kosaki K.
    Congenit Anom (Kyoto); 2005 Mar; 45(1):35-8. PubMed ID: 15737130
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  • 11. Cytogenetic and molecular characterization of a de-novo cryptic deletion of 7p21 associated with an apparently balanced translocation and complex craniosynostosis.
    Shetty S, Boycott KM, Gillan TL, Bowser K, Parboosingh JS, McInnes B, Chernos JE, Bernier FP.
    Clin Dysmorphol; 2007 Oct; 16(4):253-6. PubMed ID: 17786117
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  • 12. A novel 2.43 Mb deletion of 7q11.22-q11.23.
    Blyth M, Beal S, Huang S, Crolla J, Foulds N.
    Am J Med Genet A; 2008 Dec 15; 146A(24):3206-10. PubMed ID: 19012340
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  • 19. Molecular characterization of a patient with 3p deletion syndrome and a review of the literature.
    Fernandez TV, García-González IJ, Mason CE, Hernández-Zaragoza G, Ledezma-Rodríguez VC, Anguiano-Alvarez VM, E'Vega R, Gutiérrez-Angulo M, Maya ML, García-Bejarano HE, González-Cruz M, Barrios S, Atorga R, López-Cardona MG, Armendariz-Borunda J, State MW, Dávalos NO.
    Am J Med Genet A; 2008 Nov 01; 146A(21):2746-52. PubMed ID: 18837054
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  • 20. A patient with five chromosomal rearrangements and a 2q31.1 microdeletion.
    Wang T, Mao J, Liu MJ, Choy KW, Li HB, Cram DS, Li H, Chen Y.
    Clin Chim Acta; 2014 Mar 20; 430():129-33. PubMed ID: 24412318
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