Yates JR - Search Results

1

CA repeat polymorphism at the ASS locus.

Yuille MA, Hampson RM, Harris RM, Affara NA, Yates JR, Ferguson-Smith MA. Yuille MA, et al. Among authors: yates jr. Nucleic Acids Res. 1990 Dec 25;18(24):7472. doi: 10.1093/nar/18.24.7472. Nucleic Acids Res. 1990. PMID: 2259653 Free PMC article.

2

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

3

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

4

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.

5

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

6

Statistical analysis of the two stage mutation model in von Hippel-Lindau disease, and in sporadic cerebellar haemangioblastoma and renal cell carcinoma.

Maher ER, Yates JR, Ferguson-Smith MA. Maher ER, et al. Among authors: yates jr. J Med Genet. 1990 May;27(5):311-4. doi: 10.1136/jmg.27.5.311. J Med Genet. 1990. PMID: 2352258 Free PMC article.

7

Von Hippel-Lindau disease: a genetic study.

Maher ER, Iselius L, Yates JR, Littler M, Benjamin C, Harris R, Sampson J, Williams A, Ferguson-Smith MA, Morton N. Maher ER, et al. Among authors: yates jr. J Med Genet. 1991 Jul;28(7):443-7. doi: 10.1136/jmg.28.7.443. J Med Genet. 1991. PMID: 1895313 Free PMC article.

8

Clinical features and natural history of von Hippel-Lindau disease.

Maher ER, Yates JR, Harries R, Benjamin C, Harris R, Moore AT, Ferguson-Smith MA. Maher ER, et al. Among authors: yates jr. Q J Med. 1990 Nov;77(283):1151-63. doi: 10.1093/qjmed/77.2.1151. Q J Med. 1990. PMID: 2274658

9

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.

10

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

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