Deletion mapping of Aland Island eye disease to Xp21 between DXS67 (B24) and Duchenne muscular dystrophy.
about
Genetic mapping of a cone and rod dysfunction (Aland Island eye disease) to the proximal short arm of the human X chromosome.Recent advances in the gene map of inherited eye disorders: primary hereditary diseases of the retina, choroid, and vitreous.Duchenne muscular dystrophy: negative electroretinograms and normal dark adaptation. Reappraisal of assignment of X linked incomplete congenital stationary night blindness.Xp21 contiguous gene syndromes: deletion quantitation with bivariate flow karyotyping allows mapping of patient breakpoints.Aland island eye disease: clinical and electrophysiological studies of a Welsh family.
P2860
Deletion mapping of Aland Island eye disease to Xp21 between DXS67 (B24) and Duchenne muscular dystrophy.
description
1990 nî lūn-bûn
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1990 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1990 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1990年の論文
@ja
1990年論文
@yue
1990年論文
@zh-hant
1990年論文
@zh-hk
1990年論文
@zh-mo
1990年論文
@zh-tw
1990年论文
@wuu
name
Deletion mapping of Aland Isla ...... d Duchenne muscular dystrophy.
@ast
Deletion mapping of Aland Isla ...... d Duchenne muscular dystrophy.
@en
type
label
Deletion mapping of Aland Isla ...... d Duchenne muscular dystrophy.
@ast
Deletion mapping of Aland Isla ...... d Duchenne muscular dystrophy.
@en
prefLabel
Deletion mapping of Aland Isla ...... d Duchenne muscular dystrophy.
@ast
Deletion mapping of Aland Isla ...... d Duchenne muscular dystrophy.
@en
P2093
P2860
P1476
Deletion mapping of Aland Isla ...... d Duchenne muscular dystrophy.
@en
P2093
B R Powell
D A Pillers
E R McCabe
J A Towbin
J S Chamberlain
P2860
P304
P407
P577
1990-11-01T00:00:00Z