DNA studies in a family with Duchenne muscular dystrophy and a deletion at Xp21.
about
The C677T methylenetetrahydrofolate reductase variant and third trimester obstetrical complications in women with unexplained elevations of maternal serum alpha-fetoproteinA gene for autosomal recessive limb-girdle muscular dystrophy in Manitoba Hutterites maps to chromosome region 9q31-q33: evidence for another limb-girdle muscular dystrophy locus.Nance-Horan syndrome: localization within the region Xp21.1-Xp22.3 by linkage analysisReplacement of arginine 773 by cysteine or histidine in the human androgen receptor causes complete androgen insensitivity with different receptor phenotypes.Exclusion of the gelsolin gene on 9q32-34 as the cause of familial lattice corneal dystrophy type I.An exonic point mutation of the androgen receptor gene in a family with complete androgen insensitivity.Infantile hypophosphatasia: localization within chromosome region 1p36.1-34 and prenatal diagnosis using linked DNA markersLocalization of the McLeod locus (XK) within Xp21 by deletion analysis.Limb-girdle muscular dystrophy and Miyoshi myopathy in an aboriginal Canadian kindred map to LGMD2B and segregate with the same haplotype.Contiguous Xp11.4 Gene Deletion Leading to Ornithine Transcarbamylase Deficiency Detected by High-density Single-nucleotide Array.
P2860
Q21245563-E62FC79B-72FB-4199-88F4-572D100AC18FQ24539083-2880F4BE-397B-4A7E-9633-516C40C73609Q24676653-0F750359-7796-4D7D-9C0F-20A21FAC617FQ35196168-B3A598BB-AF06-47B8-84DC-53C6081C2A89Q35196209-728EB26C-D55B-444B-9D34-6B65EF9043B9Q35198427-A20D0F03-869E-4889-895C-61BC4DC793CAQ35201317-92BD86C1-2AFD-4290-B711-4959188402B6Q35245591-BA03BEB0-9BA5-499A-A600-9461BB7BD2F6Q35882131-E80345A3-6DDB-48B3-A30F-B03E193799B3Q36943124-BE843790-6859-4926-A232-B3195FD7E66A
P2860
DNA studies in a family with Duchenne muscular dystrophy and a deletion at Xp21.
description
1987 nî lūn-bûn
@nan
1987 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
1987 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
1987年の論文
@ja
1987年論文
@yue
1987年論文
@zh-hant
1987年論文
@zh-hk
1987年論文
@zh-mo
1987年論文
@zh-tw
1987年论文
@wuu
name
DNA studies in a family with Duchenne muscular dystrophy and a deletion at Xp21.
@ast
DNA studies in a family with Duchenne muscular dystrophy and a deletion at Xp21.
@en
type
label
DNA studies in a family with Duchenne muscular dystrophy and a deletion at Xp21.
@ast
DNA studies in a family with Duchenne muscular dystrophy and a deletion at Xp21.
@en
prefLabel
DNA studies in a family with Duchenne muscular dystrophy and a deletion at Xp21.
@ast
DNA studies in a family with Duchenne muscular dystrophy and a deletion at Xp21.
@en
P2093
P2860
P1476
DNA studies in a family with Duchenne muscular dystrophy and a deletion at Xp21
@en
P2093
Greenberg CR
Hamerton JL
Wrogemann K
P2860
P304
P407
P577
1987-08-01T00:00:00Z