RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Marciniak, Bruno
A1 Dalens, Bernard J.
SR Print(0)
ID 58066478
T1 Chondrodysplasia Grebe Type
T2 Syndromes: Rapid Recognition and Perioperative Implications
YR 2006
FD 2006
PB The McGraw-Hill Companies
PP New York, NY
SN 9780071354554
LK accessanesthesiology.mhmedical.com/content.aspx?aid=58066478
RD 2024/04/19
AB A  rare  form  of  autosomal  recessive  osteochondrodysplasia  characterized  by  severe  dwarfism  with  marked  hypomelia  and  deformation.