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

2

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. Among authors: haan ea. Am J Med Genet. 1992 Jul 1;43(4):709-15. doi: 10.1002/ajmg.1320430412. Am J Med Genet. 1992. PMID: 1377870

3

The OEIS complex (omphalocele-exstrophy-imperforate anus-spinal defects): recurrence in sibs.

Smith NM, Chambers HM, Furness ME, Haan EA. Smith NM, et al. Among authors: haan ea. J Med Genet. 1992 Oct;29(10):730-2. doi: 10.1136/jmg.29.10.730. J Med Genet. 1992. PMID: 1433234 Free PMC article.

4

Use of linkage data obtained in single families: prenatal diagnosis of a new X-linked mental retardation syndrome.

Mulley JC, Gedeon AK, Wilson S, Haan EA. Mulley JC, et al. Among authors: haan ea. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):415-9. doi: 10.1002/ajmg.1320430163. Am J Med Genet. 1992. PMID: 1605220

5

Association of Treacher Collins syndrome and translocation 6p21.31/16p13.11: exclusion of the locus from these candidate regions.

Dixon MJ, Haan E, Baker E, David D, McKenzie N, Williamson R, Mulley J, Farrall M, Callen D. Dixon MJ, et al. Among authors: haan e. Am J Hum Genet. 1991 Feb;48(2):274-80. Am J Hum Genet. 1991. PMID: 1671319 Free PMC article.

6

Hereditary unstable DNA: a new explanation for some old genetic questions?

Sutherland GR, Haan EA, Kremer E, Lynch M, Pritchard M, Yu S, Richards RI. Sutherland GR, et al. Among authors: haan ea. Lancet. 1991 Aug 3;338(8762):289-92. doi: 10.1016/0140-6736(91)90426-p. Lancet. 1991. PMID: 1677119

7

Molecular and cytogenetic studies of the Prader-Willi syndrome.

Trent RJ, Volpato F, Smith A, Lindeman R, Wong MK, Warne G, Haan E. Trent RJ, et al. Among authors: haan e. J Med Genet. 1991 Oct;28(10):649-54. doi: 10.1136/jmg.28.10.649. J Med Genet. 1991. PMID: 1682493 Free PMC article.

8

Epidemiology of Down syndrome in South Australia, 1960-89.

Staples AJ, Sutherland GR, Haan EA, Clisby S. Staples AJ, et al. Among authors: haan ea. Am J Hum Genet. 1991 Nov;49(5):1014-24. Am J Hum Genet. 1991. PMID: 1833972 Free PMC article.

9

Predictive diagnosis of myotonic dystrophy with flanking microsatellite markers.

Mulley JC, Gedeon AK, White SJ, Haan EA, Richards RI. Mulley JC, et al. Among authors: haan ea. J Med Genet. 1991 Jul;28(7):448-52. doi: 10.1136/jmg.28.7.448. J Med Genet. 1991. PMID: 1895314 Free PMC article.

10

Chromosomal origin of small ring marker chromosomes in man: characterization by molecular genetics.

Callen DF, Eyre HJ, Ringenbergs ML, Freemantle CJ, Woodroffe P, Haan EA. Callen DF, et al. Among authors: haan ea. Am J Hum Genet. 1991 Apr;48(4):769-82. Am J Hum Genet. 1991. PMID: 2014800 Free PMC article.

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