Baker E - Search Results

1

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. Am J Med Genet. 2002 Feb 1;107(4):285-93. doi: 10.1002/ajmg.10159. Am J Med Genet. 2002. PMID: 11840484

2

Recombinants of intrachromosomal transposition of subtelomeres in chromosomes 1 and 2: a cause of minute terminal chromosomal imbalances.

Daniel A, Baker E, Chia N, Haan E, Malafiej P, Hinton L, Clarke N, Adès L, Darmanian A, Callen D. Daniel A, et al. Among authors: baker e. Am J Med Genet A. 2003 Feb 15;117A(1):57-64. doi: 10.1002/ajmg.a.10048. Am J Med Genet A. 2003. PMID: 12548741 Review.

3

Re-evaluation of GM2346 from a del(16)(q22) to t(4;16)(q35;q22.1).

Callen DF, Baker EG, Lane SA. Callen DF, et al. Among authors: baker eg. Clin Genet. 1990 Dec;38(6):466-8. doi: 10.1111/j.1399-0004.1990.tb03614.x. Clin Genet. 1990. PMID: 2289320

4

Characterisation of a new rare fragile site easily confused with the fragile X.

Sutherland GR, Baker E. Sutherland GR, et al. Among authors: baker e. Hum Mol Genet. 1992 May;1(2):111-3. doi: 10.1093/hmg/1.2.111. Hum Mol Genet. 1992. PMID: 1301146

5

The common fragile site in band q27 of the human X chromosome is not coincident with the fragile X.

Sutherland GR, Baker E. Sutherland GR, et al. Among authors: baker e. Clin Genet. 1990 Mar;37(3):167-72. doi: 10.1111/j.1399-0004.1990.tb03498.x. Clin Genet. 1990. PMID: 2323087

6

The isochromosome 18p syndrome: confirmation of cytogenetic diagnosis in nine cases by in situ hybridization.

Callen DF, Freemantle CJ, Ringenbergs ML, Baker E, Eyre HJ, Romain D, Haan EA. Callen DF, et al. Among authors: baker e. Am J Hum Genet. 1990 Sep;47(3):493-8. Am J Hum Genet. 1990. PMID: 2393023 Free PMC article.

7

The morquio A syndrome (mucopolysaccharidosis IVA) gene maps to 16q24.3.

Baker E, Guo XH, Orsborn AM, Sutherland GR, Callen DF, Hopwood JJ, Morris CP. Baker E, et al. Am J Hum Genet. 1993 Jan;52(1):96-8. Am J Hum Genet. 1993. PMID: 8434612 Free PMC article.

8

The clinical significance of fragile sites on human chromosomes.

Sutherland GR, Baker E. Sutherland GR, et al. Among authors: baker e. Clin Genet. 2000 Sep;58(3):157-61. doi: 10.1034/j.1399-0004.2000.580301.x. Clin Genet. 2000. PMID: 11076037 Review.

9

A familial cryptic subtelomeric deletion 12p with variable phenotypic effect.

Baker E, Hinton L, Callen DF, Haan EA, Dobbie A, Sutherland GR. Baker E, et al. Clin Genet. 2002 Mar;61(3):198-201. doi: 10.1034/j.1399-0004.2002.610305.x. Clin Genet. 2002. PMID: 12000361

10

Frequency of truly cryptic subtelomere abnormalities--a study of 534 patients and literature review.

Yu S, Baker E, Hinton L, Eyre HJ, Waters W, Higgins S, Sutherland GR, Haan E. Yu S, et al. Among authors: baker e. Clin Genet. 2005 Nov;68(5):436-41. doi: 10.1111/j.1399-0004.2005.00513.x. Clin Genet. 2005. PMID: 16207211 Review.

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