Yates JR - Search Results

1

Multipoint linkage analysis of steroid sulfatase (X-linked ichthyosis) and distal Xp markers.

Yates JR, Goudie DR, Gillard EF, Aitken DA, Affara NA, Clayton JF, Tippett PA, Ferguson-Smith MA. Yates JR, et al. Genomics. 1987 Sep;1(1):52-9. doi: 10.1016/0888-7543(87)90104-2. Genomics. 1987. PMID: 3478297

2

Deletion of a DNA sequence in eight of nine families with X-linked ichthyosis (steroid sulphatase deficiency).

Gillard EF, Affara NA, Yates JR, Goudie DR, Lambert J, Aitken DA, Ferguson-Smith MA. Gillard EF, et al. Among authors: yates jr. Nucleic Acids Res. 1987 May 26;15(10):3977-85. doi: 10.1093/nar/15.10.3977. Nucleic Acids Res. 1987. PMID: 2884621 Free PMC article.

3

X chromosome deletions detectable by flow cytometry in some patients with steroid sulphatase deficiency (X-linked ichthyosis).

Cooke A, Gillard EF, Yates JR, Mitchell MJ, Aitken DA, Weir DM, Affara NA, Ferguson-Smith MA. Cooke A, et al. Among authors: yates jr. Hum Genet. 1988 May;79(1):49-52. doi: 10.1007/BF00291709. Hum Genet. 1988. PMID: 3163320

4

Mapping of the von Hippel-Lindau disease locus to a small region of chromosome 3p by genetic linkage analysis.

Maher ER, Bentley E, Yates JR, Latif F, Lerman M, Zbar B, Affara NA, Ferguson-Smith MA. Maher ER, et al. Among authors: yates jr. Genomics. 1991 Aug;10(4):957-60. doi: 10.1016/0888-7543(91)90185-h. Genomics. 1991. PMID: 1680799

5

Physical mapping of deletion breakpoints in patients with X-linked ichthyosis: evidence for clustering of distal and proximal breakpoints.

Newman RS, Affara NA, Yates JR, Mitchell M, Ferguson-Smith MA. Newman RS, et al. Among authors: yates jr. Proc Biol Sci. 1990 Dec 22;242(1305):231-9. doi: 10.1098/rspb.1990.0129. Proc Biol Sci. 1990. PMID: 1983039

6

Linkage of the tuberous sclerosis locus to a DNA polymorphism detected by v-abl.

Connor JM, Pirrit LA, Yates JR, Fryer AE, Ferguson-Smith MA. Connor JM, et al. Among authors: yates jr. J Med Genet. 1987 Sep;24(9):544-6. doi: 10.1136/jmg.24.9.544. J Med Genet. 1987. PMID: 2889832 Free PMC article.

7

Multipoint linkage analysis of the short arm of the human X chromosome in families with X-linked muscular dystrophy.

Wilcox DE, Affara NA, Yates JR, Ferguson-Smith MA, Pearson PL. Wilcox DE, et al. Among authors: yates jr. Hum Genet. 1985;70(4):365-75. doi: 10.1007/BF00295379. Hum Genet. 1985. PMID: 3860471

8

Emery-Dreifuss muscular dystrophy: linkage to markers in distal Xq28.

Yates JR, Warner JP, Smith JA, Deymeer F, Azulay JP, Hausmanowa-Petrusewicz I, Zaremba J, Borkowska J, Affara NA, Ferguson-Smith MA. Yates JR, et al. J Med Genet. 1993 Feb;30(2):108-11. doi: 10.1136/jmg.30.2.108. J Med Genet. 1993. PMID: 8445613 Free PMC article.

9

Physical mapping within the tuberous sclerosis linkage group in region 9q32-q34.

Harris RM, Carter NP, Griffiths B, Goudie D, Hampson RM, Yates JR, Affara NA, Ferguson-Smith MA. Harris RM, et al. Among authors: yates jr. Genomics. 1993 Feb;15(2):265-74. doi: 10.1006/geno.1993.1056. Genomics. 1993. PMID: 8449490

10

Emery-Dreifuss muscular dystrophy: localisation to Xq27.3----qter confirmed by linkage to the factor VIII gene.

Yates JR, Affara NA, Jamieson DM, Ferguson-Smith MA, Hausmanowa-Petrusewicz I, Zaremba J, Borkowska J, Johnston AW, Kelly K. Yates JR, et al. J Med Genet. 1986 Dec;23(6):587-90. doi: 10.1136/jmg.23.6.587. J Med Genet. 1986. PMID: 2879931 Free PMC article.

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