about
Clinical and Molecular genetics of Stickler syndromeClinical features of hereditary progressive arthro-ophthalmopathy (Stickler syndrome): a survey.Blindness caused by deficiency in AE3 chloride/bicarbonate exchanger.Rhegmatogenous retinal detachments associated to Stickler syndrome in a tertiary eye care center in Saudi Arabia.Evaluation and management of pediatric rhegmatogenous retinal detachmentThe biochemical structure of mammalian vitreous.Evidence of reduced bone turnover and disturbed mineralization process in a boy with Stickler syndrome.
P2860
Q24681792-423BC367-19F1-48EF-808B-27792BC7ED26Q30991204-22F10BD4-24B5-4BE3-8A22-A8154444B4DAQ33296999-92B5B3B2-013B-4D5E-952F-1F2435481A90Q35884928-AEB9624F-6A8B-4046-BC0B-0705125932C3Q37060234-95B0FDEB-0330-4E63-9F2B-1B2DC6BF40A7Q41416255-06AA0DB8-389E-4EDE-B977-CAD92646ACA7Q46273800-FB212C53-808F-4489-8424-11D8B98E17B4
P2860
description
1996 nî lūn-bûn
@nan
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
1996年论文
@zh
1996年论文
@zh-cn
name
Hereditary vitreopathy.
@en
type
label
Hereditary vitreopathy.
@en
prefLabel
Hereditary vitreopathy.
@en
P2860
P356
P1433
P1476
Hereditary vitreopathy.
@en
P2093
P2860
P2888
P304
P356
10.1038/EYE.1996.158
P478
10 ( Pt 6)
P577
1996-01-01T00:00:00Z
P5875
P6179
1050511247