Woollatt E - Search Results

1

Villard L, Briault S, Lossi AM, Paringaux C, Belougne J, Colleaux L, Pincus DR, Woollatt E, Lespinasse J, Munnich A, Moraine C, Fontès M, Gecz J. Villard L, et al. Among authors: woollatt e. J Med Genet. 1999 Oct;36(10):754-8. doi: 10.1136/jmg.36.10.754. J Med Genet. 1999. PMID: 10528854 Free PMC article.

2

Partial androgen insensitivity syndrome and t(X;5): are there upstream regulatory elements of the androgen receptor gene?

Lower KM, Kumar R, Woollatt E, Villard L, Gecz J, Sutherland GR, Callen DF. Lower KM, et al. Among authors: woollatt e. Horm Res. 2004;62(4):208-14. doi: 10.1159/000081064. Epub 2004 Sep 24. Horm Res. 2004. PMID: 15452386

3

Study of 250 children with idiopathic mental retardation reveals nine cryptic and diverse subtelomeric chromosome anomalies.

Baker E, Hinton L, Callen DF, Altree M, Dobbie A, Eyre HJ, Sutherland GR, Thompson E, Thompson P, Woollatt E, Haan E. Baker E, et al. Among authors: woollatt e. Am J Med Genet. 2002 Feb 1;107(4):285-93. doi: 10.1002/ajmg.10159. Am J Med Genet. 2002. PMID: 11840484

4

Paracentric inversions in man.

Callen DF, Woollatt E, Sutherland GR. Callen DF, et al. Among authors: woollatt e. Clin Genet. 1985 Jul;28(1):87-92. doi: 10.1111/j.1399-0004.1985.tb01224.x. Clin Genet. 1985. PMID: 4040824

5

Inherited balanced translocation t(9;17)(q33.2;q25.3) concomitant with a 16p13.1 duplication in a patient with schizophrenia.

Fullston T, Gabb B, Callen D, Ullmann R, Woollatt E, Bain S, Ropers HH, Cooper M, Chandler D, Carter K, Jablensky A, Kalaydjieva L, Gecz J. Fullston T, et al. Among authors: woollatt e. Am J Med Genet B Neuropsychiatr Genet. 2011 Mar;156(2):204-14. doi: 10.1002/ajmg.b.31157. Epub 2011 Jan 13. Am J Med Genet B Neuropsychiatr Genet. 2011. PMID: 21302349

6

Common chromosomal fragile site FRA16D sequence: identification of the FOR gene spanning FRA16D and homozygous deletions and translocation breakpoints in cancer cells.

Ried K, Finnis M, Hobson L, Mangelsdorf M, Dayan S, Nancarrow JK, Woollatt E, Kremmidiotis G, Gardner A, Venter D, Baker E, Richards RI. Ried K, et al. Among authors: woollatt e. Hum Mol Genet. 2000 Jul 1;9(11):1651-63. doi: 10.1093/hmg/9.11.1651. Hum Mol Genet. 2000. PMID: 10861292

7

Characterization and chromosome location of the gene GSTZ1 encoding the human Zeta class glutathione transferase and maleylacetoacetate isomerase.

Blackburn AC, Woollatt E, Sutherland GR, Board PG. Blackburn AC, et al. Among authors: woollatt e. Cytogenet Cell Genet. 1998;83(1-2):109-14. doi: 10.1159/000015145. Cytogenet Cell Genet. 1998. PMID: 9925947

8

The Batten disease gene product (CLN3p) is a Golgi integral membrane protein.

Kremmidiotis G, Lensink IL, Bilton RL, Woollatt E, Chataway TK, Sutherland GR, Callen DF. Kremmidiotis G, et al. Among authors: woollatt e. Hum Mol Genet. 1999 Mar;8(3):523-31. doi: 10.1093/hmg/8.3.523. Hum Mol Genet. 1999. PMID: 9949212

9

Human Sec63 endoplasmic reticulum membrane protein, map position 6q21.

Woollatt E, Pine KA, Shine J, Sutherland GR, Iismaa TP. Woollatt E, et al. Chromosome Res. 1999;7(1):77. doi: 10.1023/a:1009283530544. Chromosome Res. 1999. PMID: 10219736 No abstract available.

10

Chromosomal fragile site FRA16D and DNA instability in cancer.

Mangelsdorf M, Ried K, Woollatt E, Dayan S, Eyre H, Finnis M, Hobson L, Nancarrow J, Venter D, Baker E, Richards RI. Mangelsdorf M, et al. Among authors: woollatt e. Cancer Res. 2000 Mar 15;60(6):1683-9. Cancer Res. 2000. PMID: 10749140

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