Mosaic trisomy 1q: a recurring chromosome anomaly that is a diagnostic challenge and is associated with a Fryns‐like phenotype
Kathleen M. Bone; Judy E. Chernos; Renee Perrier; A. Micheil Innes; Francois P. Bernier; Ross McLeod; Mary Ann Thomas
Author Information: Division of Anatomic Pathology and Cytopathology, Cytogenetics Laboratory
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