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아주대학교 의학문헌정보센터
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Showing results 1 to 7 of 7
Pub Year
Title
Author(s)
1997
Atypical skeletal changes in otopalatodigital syndrome type II: phenotypic overlap among otopalatodigital syndrome type II, boomerang dysplasia, atelosteogenesis type I and type III, and lethal male phenotype of Melnick-Needles syndrome.
김옥화
2018
Craniovertebral Junction Abnormalities in Surgical Patients With Congenital Muscular Torticollis
김상현
,
나은우
,
박성훈
,
임신영
2000
Efficacy of MRI in complicated congenital heart disease with visceral heterotaxy syndrome.
원제환
2011
Identification of signal peptide domain SOST mutations in autosomal dominant craniodiaphyseal dysplasia.
김옥화
2021
Posterior lung herniation in pulmonary agenesis and aplasia: Chest radiograph and cross-sectional imaging correlation
박지은
2011
Whole-exome sequencing identifies mutations of KIF22 in spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type.
김옥화
1998
Wyburn-Mason syndrome: an unusual presentation of bilateral orbital and unilateral brain arteriovenous malformations.
김옥화
,
서정호
,
유호민
1
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아주대학교 의학문헌정보센터
