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Lack of correlation between the type of COL1A1 or COL1A2 mutation and hearing loss in osteogenesis imperfecta patients (vol 24, pg 147, 2004)
被引:3
作者:
Hartikka, H
Kuurila, K
Körkkö, J
Kaitila, I
Grénman, R
Pynnönen, S
Hyland, JC
Ala-Kokko, L
机构:
[1] Vaasa Cent Hosp, Dept Otorhinolaryngol Head & Neck Surg, Vaasa 65100, Finland
[2] Oulu Univ Hosp, Collagen Res Unit, Bioctr, Oulu, Finland
[3] Oulu Univ Hosp, Dept Med Biochem & Mol Biol, Oulu, Finland
[4] Oulu Univ, Dept Clin Genet, Oulu, Finland
[5] Univ Helsinki, Cent Hosp, Dept Clin Genet, Helsinki, Finland
[6] Univ Turku, Cent Hosp, Dept Otorhinolaryngol Head & Neck Surg, FIN-20520 Turku, Finland
[7] Univ Vaasa, Dept Math & Stat, Vaasa, Finland
[8] Tulane Univ, Hlth Sci Ctr, Ctr Gene Therapy, New Orleans, LA USA
[9] Tulane Univ, Hlth Sci Ctr, Dept Pathol, New Orleans, LA USA
[10] Tulane Univ, Hlth Sci Ctr, Dept Lab Med, New Orleans, LA USA
关键词:
D O I:
10.1002/humu.20108
中图分类号:
Q3 [遗传学];
学科分类号:
071007 ;
090102 ;
摘要:
引用
收藏
页码:437 / 437
页数:1
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