The inv dup(15) or idic(15) syndrome: A clinically recognisable neurogenetic disorder-Reference-Cited by-同舟云学术

The inv dup(15) or idic(15) syndrome: A clinically recognisable neurogenetic disorder

Published:2005-08 Issue:5 Volume:27 Page:365-369
ISSN:0387-7604
Container-title:Brain and Development
language:en
Short-container-title:Brain and Development

Author:

Battaglia Agatino

Publisher

Elsevier BV

Subject

Clinical Neurology,Developmental Neuroscience,General Medicine,Pediatrics, Perinatology, and Child Health

Reference40 articles.

1. Isolation of molecular probes associated with the chromosome 15 instability in the Prader-Willi syndrome;Donlon;Proc Natl Acad Sci USA,1986

2. Large genomic duplicons map to sites of instability in the Prader-Willi/Angelman syndrome chromosome region (15q11–q13);Christian;Hum Mol Genet,1999

3. Parental imprinting and human disease;Lalande;Annu Rev Genet,1996

4. Refined molecular characterization of the breakpoints in small inv dup (15) chromosomes;Huang;Hum Genet,1997

5. Molecular cytogenetic analysis of inv dup (15) chromosomes, using probes specific for the Prader-Willi/Angelman syndrome region: clinical implications;Leana-Cox;Am J Hum Genet,1994

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