Callen DF - 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. Among authors: callen df. 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. 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

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. Am J Hum Genet. 1990 Sep;47(3):493-8. Am J Hum Genet. 1990. PMID: 2393023 Free PMC article.

4

High resolution characterization of an interstitial deletion of less than 1.9 Mb at 4p16.3 associated with Wolf-Hirschhorn syndrome.

Fang YY, Bain S, Haan EA, Eyre HJ, MacDonald M, Wright TJ, Altherr MR, Riess O, Sutherland G, Callen DF. Fang YY, et al. Among authors: callen df. Am J Med Genet. 1997 Sep 5;71(4):453-7. Am J Med Genet. 1997. PMID: 9286454

5

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. Among authors: callen df. Clin Genet. 2002 Mar;61(3):198-201. doi: 10.1034/j.1399-0004.2002.610305.x. Clin Genet. 2002. PMID: 12000361

6

Molecular cytogenetic and clinical studies of 42 patients with marker chromosomes.

Callen DF, Eyre H, Yip MY, Freemantle J, Haan EA. Callen DF, et al. Am J Med Genet. 1992 Jul 1;43(4):709-15. doi: 10.1002/ajmg.1320430412. Am J Med Genet. 1992. PMID: 1377870

7

Localization of the human GM-CSF receptor beta chain gene (CSF2RB) to chromosome 22q12.2-->q13.1.

Shen Y, Baker E, Callen DF, Sutherland GR, Willson TA, Rakar S, Gough NM. Shen Y, et al. Among authors: callen df. Cytogenet Cell Genet. 1992;61(3):175-7. doi: 10.1159/000133401. Cytogenet Cell Genet. 1992. PMID: 1424804

8

Chromosomal location of the human transketolase gene.

Lapsys NM, Layfield R, Baker E, Callen DF, Sutherland GR, Abedinia M, Nixon PF, Mattick JS. Lapsys NM, et al. Among authors: callen df. Cytogenet Cell Genet. 1992;61(4):274-5. doi: 10.1159/000133421. Cytogenet Cell Genet. 1992. PMID: 1486804

9

The gene for the human IgA Fc receptor maps to 19q13.4.

Kremer EJ, Kalatzis V, Baker E, Callen DF, Sutherland GR, Maliszewski CR. Kremer EJ, et al. Among authors: callen df. Hum Genet. 1992 Apr;89(1):107-8. doi: 10.1007/BF00207054. Hum Genet. 1992. PMID: 1577457 No abstract available.

10

Chromosomal location of the human tumor necrosis factor receptor genes.

Baker E, Chen LZ, Smith CA, Callen DF, Goodwin R, Sutherland GR. Baker E, et al. Among authors: callen df. Cytogenet Cell Genet. 1991;57(2-3):117-8. doi: 10.1159/000133127. Cytogenet Cell Genet. 1991. PMID: 1655358

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