 |
|
A case of partial trisomy 3p syndrome with rare clinical manifestations
Dong Hoon Han (Han DH), Ji Young Chang (Chang JY), Woo In Lee (Lee WI), Chong Woo Bae (Bae CW)
Clin Exp Pediatr. 2012;55(3):107-110. Published online 2012 Mar 16 DOI: https://doi.org/10.3345/kjp.2012.55.3.107
|
|
Citations to this article as recorded by
 A large Indian family with rearrangement of chromosome 4p16 and 3p26.3 and divergent clinical presentations
Thomas Iype, Vafa Alakbarzade, Mary Iype, Royana Singh, Ajith Sreekantan-Nair, Barry A. Chioza, Tribhuvan M. Mohapatra, Emma L. Baple, Michael A. Patton, Thomas T. Warner, Christos Proukakis, Abhi Kulkarni, Andrew H. Crosby
BMC Medical Genetics.2015;[Epub] CrossRef Clinical characterization of a Korean case with 3p25 deletion
Hye Jin Lee, Ja Hye Kim, Ja Hyang Cho, Beom Hee Lee, Jin-Ho Choi, Han-Wook Yoo
Journal of Genetic Medicine.2014; 11(1): 36. CrossRef A patient with a duplication of chromosome 3p (p24.1p26.2): A comparison with other partial 3p trisomies
Daniel Natera‐de Benito, M Asunción García‐Pérez, Miguel Ángel Martínez‐Granero, Luis Izquierdo‐López
American Journal of Medical Genetics Part A.2014; 164(2): 548. CrossRef Molecular karyotyping by array CGH in a Russian cohort of children with intellectual disability, autism, epilepsy and congenital anomalies
Ivan Y Iourov, Svetlana G Vorsanova, Oxana S Kurinnaia, Maria A Zelenova, Alexandra P Silvanovich, Yuri B Yurov
Molecular Cytogenetics.2012; 5(1): 46. CrossRef
|