Gillard EF - 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. Among authors: gillard ef. Genomics. 1987 Sep;1(1):52-9. doi: 10.1016/0888-7543(87)90104-2. Genomics. 1987. PMID: 3478297

2

Molecular heterogeneity of steroid sulfatase deficiency: a multicenter study on 57 unrelated patients, at DNA and protein levels.

Ballabio A, Carrozzo R, Parenti G, Gil A, Zollo M, Persico MG, Gillard E, Affara N, Yates J, Ferguson-Smith MA, et al. Ballabio A, et al. Genomics. 1989 Jan;4(1):36-40. doi: 10.1016/0888-7543(89)90311-x. Genomics. 1989. PMID: 2644167 Clinical Trial.

3

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. 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.

4

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: gillard ef. Hum Genet. 1988 May;79(1):49-52. doi: 10.1007/BF00291709. Hum Genet. 1988. PMID: 3163320

5

Linkage analysis in X-linked ichthyosis (steroid sulfatase deficiency).

Wirth B, Herrmann FH, Neugebauer M, Gillard EF, Wulff K, Stein C, von Figura K, Ferguson-Smith MA, Gal A. Wirth B, et al. Among authors: gillard ef. Hum Genet. 1988 Oct;80(2):191-2. doi: 10.1007/BF00702868. Hum Genet. 1988. PMID: 3169744

6

A 10-megabase physical map of human Xp21, including the Duchenne muscular dystrophy gene.

Burmeister M, Monaco AP, Gillard EF, van Ommen GJ, Affara NA, Ferguson-Smith MA, Kunkel LM, Lehrach H. Burmeister M, et al. Among authors: gillard ef. Genomics. 1988 Apr;2(3):189-202. doi: 10.1016/0888-7543(88)90002-x. Genomics. 1988. PMID: 3397058

7

Analysis of Scottish Duchenne and Becker muscular dystrophy families with dystrophin cDNA probes.

Cooke A, Lanyon WG, Wilcox DE, Dornan ES, Kataki A, Gillard EF, McWhinnie AJ, Morris A, Ferguson-Smith MA, Connor JM. Cooke A, et al. Among authors: gillard ef. J Med Genet. 1990 May;27(5):292-7. doi: 10.1136/jmg.27.5.292. J Med Genet. 1990. PMID: 2191136 Free PMC article.

8

Gene diagnosis in X-linked ichthyosis.

Herrmann FH, Wirth B, Wulff K, Hadlich J, Voss M, Gillard EF, Kruse TA, Ferguson-Smith MA, Gal A. Herrmann FH, et al. Among authors: gillard ef. Arch Dermatol Res. 1989;280(8):457-61. doi: 10.1007/BF00427656. Arch Dermatol Res. 1989. PMID: 2493225

9

A probe from an X-Y homology region detects RFLPs in Xq13-q22.

Feil RP, Gillard E, Affara NA, Ferguson-Smith MA, Mandel JL. Feil RP, et al. Nucleic Acids Res. 1989 Feb 11;17(3):1279. doi: 10.1093/nar/17.3.1279. Nucleic Acids Res. 1989. PMID: 2564188 Free PMC article. No abstract available.

10

Polymorphisms and deduced amino acid substitutions in the coding sequence of the ryanodine receptor (RYR1) gene in individuals with malignant hyperthermia.

Gillard EF, Otsu K, Fujii J, Duff C, de Leon S, Khanna VK, Britt BA, Worton RG, MacLennan DH. Gillard EF, et al. Genomics. 1992 Aug;13(4):1247-54. doi: 10.1016/0888-7543(92)90042-q. Genomics. 1992. PMID: 1354642

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