Aitken DA - 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: aitken da. 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: aitken da. 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: aitken da. Hum Genet. 1988 May;79(1):49-52. doi: 10.1007/BF00291709. Hum Genet. 1988. PMID: 3163320

4

Estimating the risk of a fetal autosomal trisomy at mid-trimester using maternal serum alpha-fetoprotein and age: a retrospective study of 142 pregnancies.

Zeitune M, Aitken DA, Crossley JA, Yates JR, Cooke A, Ferguson-Smith MA. Zeitune M, et al. Among authors: aitken da. Prenat Diagn. 1991 Nov;11(11):847-57. doi: 10.1002/pd.1970111106. Prenat Diagn. 1991. PMID: 1721713

5

Amniotic fluid alpha-fetoprotein, gamma-glutamyltranspeptidase, and autosomal trisomies.

Zeitune M, Aitken DA, Graham GW, Crossley JA, Ferguson-Smith MA. Zeitune M, et al. Among authors: aitken da. Prenat Diagn. 1989 Aug;9(8):559-68. doi: 10.1002/pd.1970090805. Prenat Diagn. 1989. PMID: 2477836

6

Tuberous sclerosis: analysis of linkage to red cell and plasma protein markers.

Connor JM, Yates JR, Mann L, Aitken DA, Stephenson JB. Connor JM, et al. Among authors: aitken da. Cytogenet Cell Genet. 1987;44(1):63-4. doi: 10.1159/000132343. Cytogenet Cell Genet. 1987. PMID: 3469064 No abstract available.

7

Heterozygosity at the alpha-haptoglobin locus associated with a deletion, 16q22 leads to 16qter.

Ferguson-Smith MA, Aitken DA. Ferguson-Smith MA, et al. Among authors: aitken da. Cytogenet Cell Genet. 1978;22(1-6):513. doi: 10.1159/000131011. Cytogenet Cell Genet. 1978. PMID: 752532 No abstract available.

8

The exclusion map updated.

Aitken DA, Ferguson-Smith MA. Aitken DA, et al. Cytogenet Cell Genet. 1978;22(1-6):613-7. doi: 10.1159/000131035. Cytogenet Cell Genet. 1978. PMID: 752552 No abstract available.

9

Gene mapping by exclusion: the current status.

Aitken DA, Ferguson-Smith MA, Dick HM. Aitken DA, et al. Cytogenet Cell Genet. 1976;16(1-5):256-65. doi: 10.1159/000130605. Cytogenet Cell Genet. 1976. PMID: 975886 No abstract available.

10

Duncan Guthrie Institute of Medical Genetics, Glasgow, University of Glasgow, Scotland.

Ferguson-Smith MA, Aitken DA. Ferguson-Smith MA, et al. Among authors: aitken da. Birth Defects Orig Artic Ser. 1982;18(2):24-42. Birth Defects Orig Artic Ser. 1982. PMID: 6760922 Review.

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