Multi-allelic RFLP for M27 beta, an anonymous single copy genomic clone at Xp11.3-Xcen [HGM9 provisional no. DXS255].
about
Mapping the gene causing X-linked recessive nephrolithiasis to Xp11.22 by linkage studiesA complex rearrangement associated with sex reversal and the Wolf-Hirschhorn syndrome: a cytogenetic and molecular study.Molecular diagnosis of Turner's syndromeX inactivation as a mechanism of selection against lethal alleles: further investigation of incontinentia pigmenti and X linked lymphoproliferative disease.Clinical reinvestigation and linkage analysis in the family with Episkopi blindness (Norrie disease)X linked Charcot-Marie-Tooth disease (CMTX1): a study of 15 families with 12 highly informative polymorphisms.Pyridoxine-refractory congenital sideroblastic anaemia with evidence for autosomal inheritance: exclusion of linkage to ALAS2 at Xp11.21 by polymorphism analysis.Male neonatal death and progressive weakness and immune deficiency in females: an unknown X linked condition.Monozygotic twins discordant for Aicardi syndromeMethylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation.Manifestations of X-linked congenital stationary night blindness in three daughters of an affected male: demonstration of homozygosity.Different patterns of X inactivation in MZ twins discordant for red-green color-vision deficiency.A highly polymorphic dinucleotide repeat on the proximal short arm of the human X chromosome: linkage mapping of the synapsin I/A-raf-1 genes.Germ-line mosaicism simulates genetic heterogeneity in Wiskott-Aldrich syndrome.Clonal analysis of human tumors with M27 beta, a highly informative polymorphic X chromosomal probe.Association of somatotrophinomas with loss of alleles on chromosome 11 and with gsp mutations.The severe phenotype of females with tiny ring X chromosomes is associated with inability of these chromosomes to undergo X inactivation.Use of X-linked clonal analysis in acute promyelocytic leukemia.Clonal analysis using X-linked DNA polymorphisms.Pathogenetic Aspects of Myelodysplastic Syndromes.A highly informative X-chromosome probe, M27 beta, can be used for the determination of tumour clonality.Compound haplotypes at Xp11.23 and human population growth in Eurasia.Klinefelter syndrome is a common cause for mental retardation of unknown etiology among prepubertal males.Assessment of Clonality and Its Relevance in Acute Myeloid Leukaemia and Bone Marrow Transplantation.
P2860
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P2860
Multi-allelic RFLP for M27 beta, an anonymous single copy genomic clone at Xp11.3-Xcen [HGM9 provisional no. DXS255].
description
1987 nî lūn-bûn
@nan
1987年の論文
@ja
1987年学术文章
@wuu
1987年学术文章
@zh-cn
1987年学术文章
@zh-hans
1987年学术文章
@zh-my
1987年学术文章
@zh-sg
1987年學術文章
@yue
1987年學術文章
@zh
1987年學術文章
@zh-hant
name
Multi-allelic RFLP for M27 bet ...... [HGM9 provisional no. DXS255].
@en
type
label
Multi-allelic RFLP for M27 bet ...... [HGM9 provisional no. DXS255].
@en
prefLabel
Multi-allelic RFLP for M27 bet ...... [HGM9 provisional no. DXS255].
@en
P2093
P356
P1476
Multi-allelic RFLP for M27 bet ...... [HGM9 provisional no. DXS255].
@en
P2093
P356
10.1093/NAR/15.22.9616
P50
P577
1987-11-01T00:00:00Z