Subtelomeric analysis detects a familial 10p;12p rearrangement in two relatives with a distinct syndrome
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference18 articles.
1. Cytogenetic and molecular analysis in trisomy 12p
2. The end of the beginning of chromosome ends
3. A common region of 10p deleted in DiGeorge and velocardiofacial syndromes
4. Familial cryptic translocation with del 4q34?qter and dup 12pter?p13 in sibs with tracheal stenosis: Clinical, classical and molecular cytogenetic studies and CGH analyses from archival placental tissues evidencing tertiary trisomy 4 in one abortion specimen
5. Comparative genomic hybridisation in mentally retarded patients with dysmorphic features and a normal karyotype
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. A new partial trisomy 12p with artery catheter vagus, congenital cataracts, external auditory canal, and no turbinate;Gene;2012-11
2. A new partial trisomy 12p with artery catheter vagus, congenital cataract, no turbinate and external auditory canal;Journal of Medical Colleges of PLA;2012-04
3. Duplication of the Miller-Dieker Critical Region in a Patient with a Subtelomeric Unbalanced Translocation t(10;17)(p15.3;p13.3);Molecular Syndromology;2012
4. Combined partial trisomy 11q and partial monosomy 10p in a 19-year-old female patient: Phenotypic and genotypic findings;American Journal of Medical Genetics Part A;2011-11-03
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