Cockwell A - Search Results

1

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. Among authors: cockwell a. Hum Genet. 2002 Sep;111(3):290-6. doi: 10.1007/s00439-002-0787-2. Epub 2002 Jul 20. Hum Genet. 2002. PMID: 12215843

2

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

3

Maternal uniparental disomy for chromosome 14.

Temple IK, Cockwell A, Hassold T, Pettay D, Jacobs P. Temple IK, et al. Among authors: cockwell a. J Med Genet. 1991 Aug;28(8):511-4. doi: 10.1136/jmg.28.8.511. J Med Genet. 1991. PMID: 1681108 Free PMC article.

4

A case of maternal uniparental disomy of chromosome 9 in association with confined placental mosaicism for trisomy 9.

Wilkinson TA, James RS, Crolla JA, Cockwell AE, Campbell PL, Temple IK. Wilkinson TA, et al. Among authors: cockwell ae. Prenat Diagn. 1996 Apr;16(4):371-4. doi: 10.1002/(SICI)1097-0223(199604)16:4<371::AID-PD866>3.0.CO;2-S. Prenat Diagn. 1996. PMID: 8734817

5

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.

6

Centromeric inactivation in a dicentric human Y;21 translocation chromosome.

Fisher AM, Al-Gazali L, Pramathan T, Quaife R, Cockwell AE, Barber JC, Earnshaw WC, Axelman J, Migeon BR, Tyler-Smith C. Fisher AM, et al. Among authors: cockwell ae. Chromosoma. 1997 Sep;106(4):199-206. doi: 10.1007/s004120050240. Chromosoma. 1997. PMID: 9254721

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

Incidence of circulating cells positive for GpIb and GpIIIa in infants with Down's syndrome.

Fisher AM, Cockwell AE, Jacobs PA, Parry HF. Fisher AM, et al. Among authors: cockwell ae. Eur J Haematol. 1994 Jul;53(1):46-8. doi: 10.1111/j.1600-0609.1994.tb00178.x. Eur J Haematol. 1994. PMID: 8062897

9

Rapid in situ harvesting and cytogenetic analysis of perinatal tissue samples.

Fisher AM, Cockwell AE, Moore KJ, Gregson NM, Campbell PL, Campbell CM, Herbert A, Barber JC, Crolla JA. Fisher AM, et al. Among authors: cockwell ae. Prenat Diagn. 1996 Jul;16(7):615-21. doi: 10.1002/(SICI)1097-0223(199607)16:7<615::AID-PD920>3.0.CO;2-9. Prenat Diagn. 1996. PMID: 8843470

10

FISH characterisation of dynamic mosaicism involving an inv dup(15) in a patient with mental retardation.

Cockwell AE, Dávalos IP, Rivera HR, Crolla JA. Cockwell AE, et al. Am J Med Genet. 2001 Nov 1;103(4):289-94. Am J Med Genet. 2001. PMID: 11746008

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