Literature DB >> 15658627

Partial craniosynostosis in a patient with deletion 22q11.

J Karteszi, W Kress, M Szasz, M Czako, B Melegh, G Y Kosztolanyi, E Morava.   

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Year:  2004        PMID: 15658627

Source DB:  PubMed          Journal:  Genet Couns        ISSN: 1015-8146


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  3 in total

1.  Say-Meyer syndrome: additional manifestations in a new patient and phenotypic assessment.

Authors:  Victor M Salinas-Torres
Journal:  Childs Nerv Syst       Date:  2015-04-24       Impact factor: 1.475

Review 2.  Genetic basis of single-suture synostoses: genes, chromosomes and clinical implications.

Authors:  Wanda Lattanzi; Nenad Bukvic; Marta Barba; Gianpiero Tamburrini; Camilla Bernardini; Fabrizio Michetti; Concezio Di Rocco
Journal:  Childs Nerv Syst       Date:  2012-08-08       Impact factor: 1.475

3.  Mosaic 22q11.2 microdeletion syndrome: diagnosis and clinical manifestations of two cases.

Authors:  Ashutosh Halder; Manish Jain; Madhulika Kabra; Neerja Gupta
Journal:  Mol Cytogenet       Date:  2008-08-10       Impact factor: 2.009

  3 in total

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