Literature DB >> 10232757

No evidence for chromosomal microdeletions at the second DiGeorge syndrome locus on 10p near D10S585.

O Bartsch, A Wagner, G K Hinkel, P Lichtner, J Murken, S Schuffenhauer.   

Abstract

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Mesh：

Year:  1999        PMID： 10232757     DOI： 10.1002/(sici)1096-8628(19990423)83:5<425::aid-ajmg17>3.0.co;2-q

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN： 0148-7299


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  3 in total

1.  [DiGeorge syndrome/velcardiofacial syndrome: oral and maxillofacial surgery].

Authors:  W Pradel; O Bartsch; R Müller; G Lauer; U Eckelt
Journal:  HNO       Date:  2003-09       Impact factor: 1.284

Review 2.  Immunodeficiency in DiGeorge Syndrome and Options for Treating Cases with Complete Athymia.

Authors:  E Graham Davies
Journal:  Front Immunol       Date:  2013-10-31       Impact factor: 7.561

3.  Genomic findings in patients with clinical suspicion of 22q11.2 deletion syndrome.

Authors:  Magdalena Koczkowska; Jolanta Wierzba; Robert Śmigiel; Maria Sąsiadek; Magdalena Cabała; Ryszard Ślężak; Mariola Iliszko; Iwona Kardaś; Janusz Limon; Beata S Lipska-Ziętkiewicz
Journal:  J Appl Genet       Date:  2016-09-14       Impact factor: 3.240
  3 in total

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