Affara NA - 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: affara na. 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. Among authors: affara na. 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: affara na. Hum Genet. 1988 May;79(1):49-52. doi: 10.1007/BF00291709. Hum Genet. 1988. PMID: 3163320

5

Evolution of DNA sequence homologies between the sex chromosomes in primate species.

Lambson B, Affara NA, Mitchell M, Ferguson-Smith MA. Lambson B, et al. Among authors: affara na. Genomics. 1992 Dec;14(4):1032-40. doi: 10.1016/s0888-7543(05)80127-2. Genomics. 1992. PMID: 1478645

6

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: affara na. Genomics. 1991 Aug;10(4):957-60. doi: 10.1016/0888-7543(91)90185-h. Genomics. 1991. PMID: 1680799

7

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: affara na. Proc Biol Sci. 1990 Dec 22;242(1305):231-9. doi: 10.1098/rspb.1990.0129. Proc Biol Sci. 1990. PMID: 1983039

8

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: affara na. Genomics. 1988 Apr;2(3):189-202. doi: 10.1016/0888-7543(88)90002-x. Genomics. 1988. PMID: 3397058

9

Ordering of Y-specific sequences by deletion mapping and analysis of X-Y interchange males and females.

Ferguson-Smith MA, Affara NA, Magenis RE. Ferguson-Smith MA, et al. Among authors: affara na. Development. 1987;101 Suppl:41-50. doi: 10.1242/dev.101.Supplement.41. Development. 1987. PMID: 3503721

10

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: affara na. Hum Genet. 1985;70(4):365-75. doi: 10.1007/BF00295379. Hum Genet. 1985. PMID: 3860471

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