Literature DB >> 10494099

Molecular analysis of a translocation (6;11)(p21;q25) in a girl with Jacobsen syndrome.

C M Aalfs, J M Hoovers, F A Wijburg.   

Abstract

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Year:  1999        PMID： 10494099     DOI： 10.1002/(sici)1096-8628(19991008)86:4<398::aid-ajmg17>3.0.co;2-9

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


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  2 in total

1.  Immune Deficiency in Jacobsen Syndrome: Molecular and Phenotypic Characterization.

Authors:  Raquel Rodríguez-López; Fátima Gimeno-Ferrer; Elena Montesinos; Irene Ferrer-Bolufer; Carola Guzmán Luján; David Albuquerque; Carolina Monzó Cataluña; Virginia Ballesteros; Monserrat Aleu Pérez-Gramunt
Journal:  Genes (Basel)       Date:  2021-07-31       Impact factor: 4.096

2.  Subtle familial translocation t(11;22)(q24.2;q13.33) resulting in Jacobsen syndrome and distal trisomy 22q13.3: further details of genotype-phenotype maps.

Authors:  Aleksander Jamsheer; Marta Smyk; Jolanta Wierzba; Jolanta Kołowska; Anna Woźniak; Joanna Skołozdrzy; Maria Fischer; Anna Latos-Bieleńska
Journal:  J Appl Genet       Date:  2008       Impact factor: 3.240
  2 in total

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