Publisher's Synopsis
This new atlas concentrates on the most commonly encountered genetic syndromes in children, giving the non-specialist in clinical genetics helpful visual information to refer to when examining patients with possible hereditary or teratogenic syndromes. It features full-color illustrations of all syndromes, an important aid in pattern recognition of clinical features, as well as succinct descriptive text written for the non-specialist. Reading lists and references for each syndrome are included, enabling the clinician to quickly find further essential information and differential diagnosis.
