Literature DB >> 11038444

Familial dup(8)(p12p21.1): mild phenotypic effect and review of partial 8p duplications.

U Moog1, J J Engelen, J C Albrechts, L G Baars, C E de Die-Smulders.   

Abstract

We describe a family with direct transmission of a duplication of 8p12-->8p21.1. The phenotype of affected relatives included mild mental retardation but no minor anomalies. The duplication was identified by means of GTG-banding and fluorescence in situ hybridization with a probe specific for 8p12 generated by microdissection and degenerate oligonucleotide primed-polymerase chain reaction. Assay of glutathione reductase, which has been localised to 8p21.1, was significantly increased when compared with controls with normal chromosomal constitution. To the best of our knowledge, a proximal direct duplication of 8p restricted to subbands p12-->p21.1 has not been reported so far. The reported aberration is compared with other partial duplications of 8p, in particular to inversion duplications 8p and to small direct distal duplications involving 8p23.1. Am. J. Med. Genet. 94:306-310, 2000. Copyright 2000, Wiley-Liss, Inc.

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Year:  2000        PMID: 11038444     DOI: 10.1002/1096-8628(20001002)94:4<306::aid-ajmg8>3.0.co;2-v

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


  7 in total

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6.  46,XY,r(8)/45,XY,-8 Mosaicism as a Possible Mechanism of the Imprinted Birk-Barel Syndrome: A Case Study.

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7.  De novo 8p21.3→ p23.3 Duplication With t(4;8)(q35;p21.3) Translocation Associated With Mental Retardation, Autism Spectrum Disorder, and Congenital Heart Defects: Case Report With Literature Review.

Authors:  Cristina Gug; Dorina Stoicanescu; Ioana Mozos; Laura Nussbaum; Mariana Cevei; Danae Stambouli; Anca Gabriela Pavel; Gabriela Doros
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  7 in total

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