J. Opitz

发表

PTPN11 mutations are not responsible for the Cardiofaciocutaneous (CFC) syndrome

J. Opitz, D. Brunoni, M. Zollino, 2003, European Journal of Human Genetics.

Facial midline defect in the fetal alcohol syndrome: embryogenetic considerations in two clinical cases.

C. Romano, J. Opitz, G. Neri, 1988, American journal of medical genetics.

Simpson‐golabi‐behmel syndrome: An X‐linked encephalo‐tropho‐schisis syndrome

J. Opitz, G. Neri, M. Cappa, 1988, American journal of medical genetics. Part A.