Literature DB >> 14585631

DiGeorge's syndrome: a gene at last.

Antonio Baldini1.   

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Year:  2003        PMID： 14585631     DOI： 10.1016/S0140-6736(03)14671-5

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  4 in total

1.  Beta-catenin deficiency causes DiGeorge syndrome-like phenotypes through regulation of Tbx1.

Authors:  Sung-Ho Huh; David M Ornitz
Journal:  Development       Date:  2010-04       Impact factor: 6.868

2.  Pulmonary anatomy and a case of unilateral aplasia in a common snapping turtle (Chelydra serpentina): developmental perspectives on cryptodiran lungs.

Authors:  E R Schachner; J C Sedlmayr; R Schott; T R Lyson; R K Sanders; M Lambertz
Journal:  J Anat       Date:  2017-10-24       Impact factor: 2.610

3.  An interstitial deletion-insertion involving chromosomes 2p25.3 and Xq27.1, near SOX3, causes X-linked recessive hypoparathyroidism.

Authors:  Michael R Bowl; M Andrew Nesbit; Brian Harding; Elaine Levy; Andrew Jefferson; Emanuela Volpi; Karine Rizzoti; Robin Lovell-Badge; David Schlessinger; Michael P Whyte; Rajesh V Thakker
Journal:  J Clin Invest       Date:  2005-09-15       Impact factor: 14.808

Review 4.  The physiological and pathological functions of VEGFR3 in cardiac and lymphatic development and related diseases.

Authors:  Richard M Monaghan; Donna J Page; Pia Ostergaard; Bernard D Keavney
Journal:  Cardiovasc Res       Date:  2021-07-07       Impact factor: 10.787
  4 in total

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