Terminal microdeletions of 13q34 chromosome region in patients with intellectual disability: Delineation of an emerging new microdeletion syndrome.
暂无分享,去创建一个
[1] R. Redon,et al. De Novo Truncating Mutations in the Kinetochore‐Microtubules Attachment Gene CHAMP1 Cause Syndromic Intellectual Disability , 2016, Human mutation.
[2] L. Garavelli,et al. Cryptic 13q34 and 4q35.2 Deletions in an Italian Family , 2015, Cytogenetic and Genome Research.
[3] R. Pfundt,et al. De Novo Mutations in CHAMP1 Cause Intellectual Disability with Severe Speech Impairment. , 2015, American journal of human genetics.
[4] T. Shaikh,et al. Mutations in the mitochondrial cysteinyl-tRNA synthase gene, CARS2, lead to a severe epileptic encephalopathy and complex movement disorder , 2015, Journal of Medical Genetics.
[5] U. Felbor,et al. Large deletions play a minor but essential role in congenital coagulation factor VII and X deficiencies , 2015, Hämostaseologie.
[6] Li Xie,et al. A 1.1Mb deletion in distal 13q deletion syndrome region with congenital heart defect and postaxial polydactyly: additional support for a CHD locus at distal 13q34 region. , 2013, Gene.
[7] Brenda R. J. Jansen,et al. Math practice and its influence on math skills and executive functions in adolescents with mild to borderline intellectual disability. , 2013, Research in developmental disabilities.
[8] J. Bakkers,et al. Genetics of congenital heart defects: a candidate gene approach. , 2010, Trends in cardiovascular medicine.
[9] J. Fryns,et al. Phenotype and 244k array‐CGH characterization of chromosome 13q deletions: An update of the phenotypic map of 13q21.1‐qter , 2009, American journal of medical genetics. Part A.
[10] D. Lacombe,et al. Twelve new patients with 13q deletion syndrome: genotype-phenotype analyses in progress. , 2009, European journal of medical genetics.
[11] A. Latos-Bieleńska,et al. Chromosome deletions in 13q33–34: Report of four patients and review of the literature , 2008, American journal of medical genetics. Part A.
[12] Takaaki Hayashi,et al. A novel homozygous GRK1 mutation (P391H) in 2 siblings with Oguchi disease with markedly reduced cone responses. , 2007, Ophthalmology.
[13] J. Toretsky,et al. Factor VII deficiency and developmental abnormalities in a patient with partial monosomy of 13q and trisomy of 16p: case report and review of the literature , 2006, BMC Medical Genetics.
[14] M. Hewson,et al. Severe congenital Factor VII deficiency associated with the 13q deletion syndrome , 2002, American journal of hematology.
[15] D. Ginsburg,et al. Prothrombotic phenotype of protein Z deficiency. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[16] M. Briquel,et al. Structural genes of coagulation factors VII and X located on 13q34. , 1986, Annales de genetique.