Literature DB >> 2260575

Ring chromosome 22 karyotype in a patient with Opitz (BBBG) syndrome.

J Christodoulou, A Bankier, P Loughnan.   

Abstract

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Mesh：

Year:  1990        PMID： 2260575     DOI： 10.1002/ajmg.1320370324

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


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  3 in total

1.  Anal anomalies: an uncommon feature of velocardiofacial (Shprintzen) syndrome?

Authors:  S Worthington; A Colley; K Fagan; K Dai; A H Lipson
Journal:  J Med Genet       Date:  1997-01       Impact factor: 6.318

2.  Congenital alacrima in a patient with G (Opitz Frias) syndrome.

Authors:  M Dundar; K Erkihç; F Demiryilmaz; M Küçükaydin; M Kendirci; H Okur; A Kazez
Journal:  Hum Genet       Date:  1996-04       Impact factor: 4.132

3.  Auditory findings and electrophysiologics in individuals with G/BBB syndrome.

Authors:  Tatiana Vialôgo Cassab; Sthella Zanchetta; Célia Maria Giacheti; Neivo Luiz Zorzetto; Antonio Richieri-Costa
Journal:  Braz J Otorhinolaryngol       Date:  2011 Nov-Dec
  3 in total

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