Search research articles
Contact Us
Filters
Showing results (1-10 of 5) with videos related to
Page
of 1
Sort By:
Journal of the Medical Association of Thailand = Chotmaihet Thangphaet
|
September 15, 2001
Mandibular distraction osteogenesis in unilateral craniofacial microsomia: preliminary report
C Mahatumarat, P Chokrungvaranont, N Rojvachiranonda
The Journal of Craniofacial Surgery
|
July 1, 1999
Spontaneous closure of bony defect in a frontoethmoidal encephalomeningocele patient
C Mahatumarat, C Taecholarn, N Rojvachiranonda
The Journal of Craniofacial Surgery
|
December 1, 1991
One-stage extracranial repair and reconstruction for frontoethmoidal encephalomeningocele: a new simple technique
C Mahatumarat, C Taecholarn, T Charoonsmith
Plastic and Reconstructive Surgery
|
October 1, 1987
Hemifacial microsomia: a multisystem classification
D J David, C Mahatumarat, R D Cooter
The Southeast Asian Journal of Tropical Medicine and Public Health
|
September 15, 2001
A case of Pfeiffer syndrome type 1 with an A344P mutation in the FGFR2 gene
V Shotelersuk, S Srivuthana, C Ittiwut, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 5) with videos related to
Sort By:
Page
of 1
Journal of the Medical Association of Thailand = Chotmaihet Thangphaet
|
September 15, 2001
Mandibular distraction osteogenesis in unilateral craniofacial microsomia: preliminary report
C Mahatumarat, P Chokrungvaranont, N Rojvachiranonda
The Journal of Craniofacial Surgery
|
July 1, 1999
Spontaneous closure of bony defect in a frontoethmoidal encephalomeningocele patient
C Mahatumarat, C Taecholarn, N Rojvachiranonda
The Journal of Craniofacial Surgery
|
December 1, 1991
One-stage extracranial repair and reconstruction for frontoethmoidal encephalomeningocele: a new simple technique
C Mahatumarat, C Taecholarn, T Charoonsmith
Plastic and Reconstructive Surgery
|
October 1, 1987
Hemifacial microsomia: a multisystem classification
D J David, C Mahatumarat, R D Cooter
The Southeast Asian Journal of Tropical Medicine and Public Health
|
September 15, 2001
A case of Pfeiffer syndrome type 1 with an A344P mutation in the FGFR2 gene
V Shotelersuk, S Srivuthana, C Ittiwut, et al.
Page
of 1