共 50 条
- [22] A novel deletion in proximal 22q associated with cardiac septal defects and microcephaly: a case report MOLECULAR CYTOGENETICS, 2009, 2
- [23] A novel deletion in proximal 22q associated with cardiac septal defects and microcephaly: a case report Molecular Cytogenetics, 2
- [28] Clinical and molecular cytogenetic characterization of two patients with partial trisomy 1q41-qter: Further delineation of partial trisomy 1q syndrome AMERICAN JOURNAL OF MEDICAL GENETICS, 2001, 104 (04): : 312 - 318