A case of partial trisomy 3p syndrome with rare clinical manifestations
Author:
Affiliation:
1. Department of Pediatrics, Kyung Hee University School of Medicine, Seoul, Korea.
2. Department of Laboratory Medicine, Kyung Hee University School of Medicine, Seoul, Korea.
Publisher
Korean Pediatric Society
Subject
Pediatrics,Pediatrics, Perinatology, and Child Health
Link
http://kjp.or.kr/upload/pdf/kjped-55-107.pdf
Reference10 articles.
1. Molecular characterization of trisomic segment 3p24.1→3pter: a case with review of the literature
2. Partial trisomy 3p syndrome
3. Partial 3p trisomy and different rearrangements involving chromosome 3 in the proposita's family
4. A New Translocation Syndrome (3/B)
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1. A large Indian family with rearrangement of chromosome 4p16 and 3p26.3 and divergent clinical presentations;BMC Medical Genetics;2015-11-10
2. Clinical characterization of a Korean case with 3p25 deletion;Journal of Genetic Medicine;2014-06-30
3. A patient with a duplication of chromosome 3p (p24.1p26.2): A comparison with other partial 3p trisomies;American Journal of Medical Genetics Part A;2013-12-05
4. Case Report 3p partial trisomy and 13q partial monosomy with congenital malformations and psychomotor developmental delay;Genetics and Molecular Research;2013
5. Molecular karyotyping by array CGH in a Russian cohort of children with intellectual disability, autism, epilepsy and congenital anomalies;Molecular Cytogenetics;2012
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