RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164084421
T1 SC Phocomelia Syndrome
T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e
YR 2019
FD 2019
PB McGraw-Hill Education
PP New York, NY
SN 9781259861789
LK accesspediatrics.mhmedical.com/content.aspx?aid=1164084421
RD 2023/09/21
AB A  very  rare,  autosomal  recessive,  severe,  polymalformative  disease  characterized  by  cranial  and  maxillofacial  deformities,  limb  anomalies,  and  intellectual  disability.