Yates JR - Search Results

1

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: yates jr. Prenat Diagn. 1991 Nov;11(11):847-57. doi: 10.1002/pd.1970111106. Prenat Diagn. 1991. PMID: 1721713

2

Second-trimester maternal serum screening using alpha-fetoprotein, human chorionic gonadotrophin, and unconjugated oestriol: experience of a regional programme.

Goodburn SF, Yates JR, Raggatt PR, Carr C, Ferguson-Smith ME, Kershaw AJ, Milton PJ, Ferguson-Smith MA. Goodburn SF, et al. Among authors: yates jr. Prenat Diagn. 1994 May;14(5):391-402. doi: 10.1002/pd.1970140509. Prenat Diagn. 1994. PMID: 7521964

3

Maternal age specific rates for chromosome aberrations and factors influencing them: report of a collaborative european study on 52 965 amniocenteses.

Ferguson-Smith MA, Yates JR. Ferguson-Smith MA, et al. Among authors: yates jr. Prenat Diagn. 1984 Spring;4 Spec No:5-44. doi: 10.1002/pd.1970040704. Prenat Diagn. 1984. PMID: 6235485 No abstract available.

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

5

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

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

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.

8

Instability of normal (CTG)n alleles in the DM kinase gene.

Dow DJ, Rubinsztein DC, Yates JR, Barton DE, Ferguson-Smith MA. Dow DJ, et al. Among authors: yates jr. J Med Genet. 1997 Oct;34(10):871-3. doi: 10.1136/jmg.34.10.871. J Med Genet. 1997. PMID: 9350827 Free PMC article.

9

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.

10

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

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