SC phocomelia syndrome, premature centromere separation, and congenital cranial nerve paralysis in two sisters, one with malignant melanoma
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference46 articles.
1. Cytogenetic and Morphologic Abnormalities in Human Bone Marrow Cells during Cytosine Arabinoside Therapy
2. Colchicine resistance in human cell lines. Pleiotropic phenotype and decreased membrane permeability
3. RECENT DEVELOPMENTS IN THE PRENATAL DIAGNOSIS OF GENETIC DISEASES AND BIRTH DEFECTS
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