Further delineation of novel 1p36 rearrangements by array-CGH analysis: Narrowing the breakpoints and clarifying the “extended” phenotype-Reference-Cited by-同舟云学术

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Further delineation of novel 1p36 rearrangements by array-CGH analysis: Narrowing the breakpoints and clarifying the “extended” phenotype

Published:2012-09 Issue:2 Volume:506 Page:360-368
ISSN:0378-1119
Container-title:Gene
language:en
Short-container-title:Gene

Author:

Giannikou Krinio,Fryssira Helen,Oikonomakis Vasilis,Syrmou Areti,Kosma Konstantina,Tzetis Maria,Kitsiou-Tzeli Sofia,Kanavakis Emmanouel

Publisher

Elsevier BV

Subject

Genetics,General Medicine

Reference30 articles.

1. Array-based comparative genomic hybridization: clinical contexts for targeted and whole-genome designs;Aradhya;Genet. Med.,2007

2. Agenesis of the corpus callosum with midline lipoma associated with an Xp22.31–Xp22.12 deletion;Baker;Clin. Dysmorphol.,2011

3. Monosomy 1p36 breakpoints indicate repetitive DNA sequence elements may be involved in generating and/or stabilizing terminal deletions;Ballif;Chromosome Res.,2004

4. Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation;Battaglia;Pediatrics,2008

5. Complex constitutional subtelomeric 1p36.3 deletion/duplication in a mentally retarded child with neonatal neuroblastoma;Bertrand;Eur. J. Med. Genet.,2008

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4. Triplications of chromosome 1p36.3, including the genes GABRD and SKI, are associated with a developmental disorder and a facial gestalt;American Journal of Medical Genetics Part A;2023-05-02

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