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K. Kaneko M.J. Wagner D.E. Wells H. Tanaka T. Miyatake S. Tsuji 《Nucleic acids research》1991,19(21):6059
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The gene for hypotrichosis of Marie Unna maps between D8S258 and D8S298: exclusion of the hr gene by cDNA and genomic sequencing. 总被引:3,自引:0,他引:3 下载免费PDF全文
M van Steensel F J Smith P M Steijlen I Kluijt H P Stevens A Messenger H Kremer M G Dunnill C Kennedy C S Munro V R Doherty J A McGrath S P Covello C M Coleman J Uitto W H McLean 《American journal of human genetics》1999,65(2):413-419
Hypotrichosis of Marie Unna (MU) is an autosomal dominant hair-loss disorder with onset in childhood. A genomewide search for the gene was performed in a large Dutch family using 400 fluorescent microsatellite markers. Linkage was detected with marker D8S258, and analysis of this family and a further British kindred with additional markers in the region gave a combined maximum two-point LOD score of 13.42, with D8S560. Informative recombinants placed the MU gene in a 2.4-cM interval between markers D8S258 and D8S298. Recently, recessive mutations in the hr gene were reported in families with congenital atrichia, and this gene was previously mapped close to the MU interval. By radiation-hybrid mapping, we placed the hr gene close to D8S298 but were unable to exclude it from the MU interval. This, with the existence of the semidominant murine hr allele, prompted us to perform mutation analysis for this gene. Full-length sequencing of hr cDNA obtained from an affected individual showed no mutations. Similarly, screening of all exons of the hr gene amplified from the genomic DNA of an affected individual revealed no mutations. Analysis of expressed sequences and positional cloning of the MU locus is underway. 相似文献
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P.J. Parry D. Markie E.R. Fearon J.M. Nigro B. Vogelstein W.F. Bodmer 《Nucleic acids research》1991,19(24):6983
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Antonella Minelli Giovanna Floridia Elena Rossi Maurizio Clementi Romano Tenconi Lamberto Camurri Franca Bernardi Heidi Hoeller Carlo Previde Re Paola Maraschio Stephen Wood Orsetta Zuffardi Cesare Danesino 《Human genetics》1993,92(4):391-396
Ten patients with inverted duplication of 8p (inv dup 8p) were studied with cytogenetic, biochemical and molecular techniques. The duplication for the region 8p12-p22 was always associated with a deletion of the locus D8S7 (mapped in 8p23.1) as demonstrated with the probe pSW50 by both in situ hybridization and Southern blot. Restriction fragment length polymorphisms detected by probes pSW50 (1 case) and by pG2LPL35 (locus LPL) (two cases) were informative as to a maternal origin of the anomaly. The activity of glutathione reductase, whose gene maps in the duplicated region at 8p21.1, was increased in all patients. The recognizable phenotype of inv dup 8p includes neonatal hypotonia, prominent forehead, large mouth with everted lower lip, abnormally shaped large ears, brain malformations and severe mental retardation. Our findings indicate that the chromosome rearrangement is homogeneous at least for the presence of the deletion and support the hypothesis of a common mechanism of origin. 相似文献
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