about
A new X linked recessive deafness syndrome with blindness, dystonia, fractures, and mental deficiency is linked to Xq22.Linkage between sexual orientation and chromosome Xq28 in males but not in femalesRegional localization of an X-linked mental retardation gene to Xp21.1-Xp22.13 (MRX38)Linkage analysis in Rett syndrome families suggests that there may be a critical region at Xq28Localisation of a new gene for non-specific mental retardation to Xq22-q26 (MRX35).DNA variability and recombination rates at X-linked loci in humansMicrosatellite variation and recombination rate in the human genome.X-linked recessive panhypopituitarism associated with a regional duplication in Xq25-q26.A radiation hybrid map spanning the entire human X chromosome integrating YACs, genes, and STS markers.Physical and genetic mapping of the human X chromosome centromere: repression of recombination.Emerin deletion reveals a common X-chromosome inversion mediated by inverted repeats.X-linked mental retardation with variable stature, head circumference, and testicular volume linked to Xq12-q21.An integrated map of chromosome 9.
P2860
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P2860
description
1994 nî lūn-bûn
@nan
1994 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
1994 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
name
Integration of gene maps: chromosome X
@ast
Integration of gene maps: chromosome X
@en
Integration of gene maps: chromosome X
@nl
type
label
Integration of gene maps: chromosome X
@ast
Integration of gene maps: chromosome X
@en
Integration of gene maps: chromosome X
@nl
prefLabel
Integration of gene maps: chromosome X
@ast
Integration of gene maps: chromosome X
@en
Integration of gene maps: chromosome X
@nl
P2093
P356
P1433
P1476
Integration of gene maps: chromosome X
@en
P2093
P304
P356
10.1006/GENO.1994.1432
P407
P577
1994-08-01T00:00:00Z