Holoprosencephaly with cerebellar vermis hypoplasia in 13q deletion syndrome: Critical region for cerebellar dysgenesis within 13q32.2q34-Reference-Cited by-同舟云学术

Holoprosencephaly with cerebellar vermis hypoplasia in 13q deletion syndrome: Critical region for cerebellar dysgenesis within 13q32.2q34

Published:2015-08 Issue:7 Volume:37 Page:714-718
ISSN:0387-7604
Container-title:Brain and Development
language:en
Short-container-title:Brain and Development

Author:

Mimaki Masakazu,Shiihara Takashi,Watanabe Mio,Hirakata Kyoko,Sakazume Satoru,Ishiguro Akio,Shimojima Keiko,Yamamoto Toshiyuki,Oka Akira,Mizuguchi Masashi

Funder

Program for Promoting the Establishment of Strategic Research Centers

Special Coordination Funds for Promoting Science and Technology, Ministry of Education, Culture, Sports, Science and Technology

Publisher

Elsevier BV

Subject

Neurology (clinical),Developmental Neuroscience,General Medicine,Pediatrics, Perinatology and Child Health

Reference14 articles.

1. The 13q-syndrome: the molecular definition of a critical deletion region in band 13q32;Brown;Am J Hum Genet,1995

2. 13q Deletion and central nervous system anomalies: further insights from karyotype–phenotype analyses of 14 patients;Ballarati;J Med Genet,2007

3. Partial deletions of the long arm of chromosome 13 associated with holoprosencephaly and the Dandy–Walker malformation;McCormack;Am J Med Genet,2002

4. Is Dandy–Walker malformation associated with “distal 13q deletion syndrome”? Findings in a fetus supporting previous observations;Alanay;Am J Med Genet A,2005

5. Twelve new patients with 13q deletion syndrome: genotype–phenotype analyses in progress;Quelin;Eur J Med Genet,2009

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