Cockwell A[au] - Search Results

Year	Number of Results
1990	2
1991	3
1992	2
1993	1
1994	3
1995	1
1996	4
1997	2
2000	1
2001	1
2002	1
2003	1
2005	1
2006	2
2007	3
2008	1
2010	1
2024	0

1

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.

2

The origin of trisomy 13.

Hall HE, Chan ER, Collins A, Judis L, Shirley S, Surti U, Hoffner L, Cockwell AE, Jacobs PA, Hassold TJ. Hall HE, et al. Among authors: cockwell ae. Am J Med Genet A. 2007 Oct 1;143A(19):2242-8. doi: 10.1002/ajmg.a.31913. Am J Med Genet A. 2007. PMID: 17853475

3

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

4

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

5

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

6

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.

7

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

8

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.

9

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.

10

Is karyotyping couples experiencing recurrent miscarriage worth the cost?

Barber JC, Cockwell AE, Grant E, Williams S, Dunn R, Ogilvie CM. Barber JC, et al. Among authors: cockwell ae. BJOG. 2010 Jun;117(7):885-8. doi: 10.1111/j.1471-0528.2010.02566.x. BJOG. 2010. PMID: 20482539

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