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Literature DB >> 2891116

Multi-allelic RFLP for M27 beta, an anonymous single copy genomic clone at Xp11.3-Xcen [HGM9 provisional no. DXS255].

N J Fraser¹, Y Boyd, G G Brownlee, I W Craig.

Abstract

Mesh：

Year: 1987 PMID： 2891116 PMCID： PMC306508 DOI： 10.1093/nar/15.22.9616

Source DB: PubMed Journal: Nucleic Acids Res ISSN： 0305-1048 Impact factor: 16.971

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26 in total

1. Monozygotic twins discordant for Aicardi syndrome.

Authors: T Costa; W Greer; G Rysiecki; J R Buncic; P N Ray
Journal: J Med Genet Date: 1997-08 Impact factor: 6.318

2. X inactivation as a mechanism of selection against lethal alleles: further investigation of incontinentia pigmenti and X linked lymphoproliferative disease.

Authors: A Harris; J Collins; D Vetrie; C Cole; M Bobrow
Journal: J Med Genet Date: 1992-09 Impact factor: 6.318

3. Different patterns of X inactivation in MZ twins discordant for red-green color-vision deficiency.

Authors: A L Jørgensen; J Philip; W H Raskind; M Matsushita; B Christensen; V Dreyer; A G Motulsky
Journal: Am J Hum Genet Date: 1992-08 Impact factor: 11.025

4. Unusual X chromosome inactivation in a mentally retarded girl with an interstitial deletion Xq27: implications for the fragile X syndrome.

Authors: M Schmidt; A Certoma; D Du Sart; P Kalitsis; M Leversha; K Fowler; L Sheffield; I Jack; D M Danks
Journal: Hum Genet Date: 1990-03 Impact factor: 4.132

Multi-allelic RFLP for M27 beta, an anonymous single copy genomic clone at Xp11.3-Xcen [HGM9 provisional no. DXS255].

1. Monozygotic twins discordant for Aicardi syndrome.

2. X inactivation as a mechanism of selection against lethal alleles: further investigation of incontinentia pigmenti and X linked lymphoproliferative disease.

3. Different patterns of X inactivation in MZ twins discordant for red-green color-vision deficiency.

4. Unusual X chromosome inactivation in a mentally retarded girl with an interstitial deletion Xq27: implications for the fragile X syndrome.

5. Maternal meiosis II nondisjunction in a case of 47,XXY testicular feminization.

6. Germ-line mosaicism simulates genetic heterogeneity in Wiskott-Aldrich syndrome.

7. Differential methylation at the 5' and the 3' CCGG sites flanking the X chromosomal hypervariable DXS255 locus.

8. Molecular diagnosis of Turner's syndrome.

9. Wiskott-Aldrich syndrome carrier detection with the hypervariable marker M27 beta.

10. Mapping the gene causing X-linked recessive nephrolithiasis to Xp11.22 by linkage studies.