Clinical, cytogenetic, and molecular characterization of a patient with a de novo interstitial 22q12 duplication
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.20672/fullpdf
Reference26 articles.
1. Duplication of distal 22q
2. Human-Specific Duplication and Mosaic Transcripts: The Recent Paralogous Structure of Chromosome 22
3. Low-Copy Repeats Mediate the Common 3-Mb Deletion in Patients with Velo-cardio-facial Syndrome
4. A common molecular basis for rearrangement disorders on chromosome 22q11
5. AT-Rich Palindromes Mediate the Constitutional t(11;22) Translocation
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1. Concurrent triplication and uniparental isodisomy: evidence for microhomology-mediated break-induced replication model for genomic rearrangements;European Journal of Human Genetics;2014-04-09
2. Skull defects, alopecia, hypertelorism, and notched alae nasi caused by homozygousALX4gene mutation;American Journal of Medical Genetics Part A;2014-03-25
3. Vertical transmission of a frontonasal phenotype caused by a novelALX4mutation;American Journal of Medical Genetics Part A;2013-02-07
4. Clinical and molecular cytogenetic characterization of four patients with unbalanced translocation der(1)t(1;22)(p36;q13);American Journal of Medical Genetics Part A;2008-11-01
5. A 7 Mb duplication at 22q13 in a girl with bipolar disorder and hippocampal malformation;American Journal of Medical Genetics Part A;2008-07-01
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