Chen, C. Prenatal diagnosis of familial 2q13 microduplication and a de novo Xp22.33 microdeletion in a pregnancy associated with an asymptomatic mother carrier. Elsevier.
Chicago Style (17th ed.) CitationChen, Chih-Ping. Prenatal Diagnosis of Familial 2q13 Microduplication and a De Novo Xp22.33 Microdeletion in a Pregnancy Associated with an Asymptomatic Mother Carrier. Elsevier.
MLA (9th ed.) CitationChen, Chih-Ping. Prenatal Diagnosis of Familial 2q13 Microduplication and a De Novo Xp22.33 Microdeletion in a Pregnancy Associated with an Asymptomatic Mother Carrier. Elsevier.
Warning: These citations may not always be 100% accurate.