Cockwell AE - Search Results

1

Investigation of the origins of human autosomal inversions.

Thomas NS, Bryant V, Maloney V, Cockwell AE, Jacobs PA. Thomas NS, et al. Among authors: cockwell ae. Hum Genet. 2008 Jul;123(6):607-16. doi: 10.1007/s00439-008-0510-z. Epub 2008 May 10. Hum Genet. 2008. PMID: 18470537

2

A study of cryptic terminal chromosome rearrangements in recurrent miscarriage couples detects unsuspected acrocentric pericentromeric abnormalities.

Cockwell AE, Jacobs PA, Beal SJ, Crolla JA. Cockwell AE, et al. Hum Genet. 2003 Mar;112(3):298-302. doi: 10.1007/s00439-002-0887-z. Epub 2003 Jan 8. Hum Genet. 2003. PMID: 12596054

3

Distribution of the D15Z1 copy number polymorphism.

Cockwell AE, Jacobs PA, Crolla JA. Cockwell AE, et al. Eur J Hum Genet. 2007 Apr;15(4):441-5. doi: 10.1038/sj.ejhg.5201780. Epub 2007 Feb 21. Eur J Hum Genet. 2007. PMID: 17311084

4

Duplications of chromosome 11p15 of maternal origin result in a phenotype that includes growth retardation.

Fisher AM, Thomas NS, Cockwell A, Stecko O, Kerr B, Temple IK, Clayton P. Fisher AM, et al. Hum Genet. 2002 Sep;111(3):290-6. doi: 10.1007/s00439-002-0787-2. Epub 2002 Jul 20. Hum Genet. 2002. PMID: 12215843

5

A cytogenetic and molecular reappraisal of a series of patients with Turner's syndrome.

Jacobs PA, Betts PR, Cockwell AE, Crolla JA, Mackenzie MJ, Robinson DO, Youings SA. Jacobs PA, et al. Among authors: cockwell ae. Ann Hum Genet. 1990 Jul;54(3):209-23. doi: 10.1111/j.1469-1809.1990.tb00379.x. Ann Hum Genet. 1990. PMID: 2221825

6

A comparison of the clinical and cytogenetic findings in nine patients with a ring (X) cell line and 16 45,X patients.

Collins AL, Cockwell AE, Jacobs PA, Dennis NR. Collins AL, et al. Among authors: cockwell ae. J Med Genet. 1994 Jul;31(7):528-33. doi: 10.1136/jmg.31.7.528. J Med Genet. 1994. PMID: 7966189 Free PMC article. Review.

7

Molecular investigation of a dicentric 13;17 chromosome found in a 21-week gestation fetus with multiple congenital abnormalities.

Cockwell AE, Maloney VK, Thomas NS, Smith EL, Gonda P, Bass P, Crolla JA. Cockwell AE, et al. Cytogenet Genome Res. 2006;112(1-2):166-9. doi: 10.1159/000087530. Cytogenet Genome Res. 2006. PMID: 16276107

8

A cytogenetic and molecular study of a series of 45,X fetuses and their parents.

Cockwell A, MacKenzie M, Youings S, Jacobs P. Cockwell A, et al. J Med Genet. 1991 Mar;28(3):151-5. doi: 10.1136/jmg.28.3.151. J Med Genet. 1991. PMID: 1675683 Free PMC article.

9

Trisomy 21: association between reduced recombination and nondisjunction.

Sherman SL, Takaesu N, Freeman SB, Grantham M, Phillips C, Blackston RD, Jacobs PA, Cockwell AE, Freeman V, Uchida I, et al. Sherman SL, et al. Among authors: cockwell ae. Am J Hum Genet. 1991 Sep;49(3):608-20. Am J Hum Genet. 1991. PMID: 1831960 Free PMC article.

10

Three patients with ring (X) chromosomes and a severe phenotype.

Dennis NR, Collins AL, Crolla JA, Cockwell AE, Fisher AM, Jacobs PA. Dennis NR, et al. Among authors: cockwell ae. J Med Genet. 1993 Jun;30(6):482-6. doi: 10.1136/jmg.30.6.482. J Med Genet. 1993. PMID: 8326492 Free PMC article.

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