Couzin D - Search Results

Year	Number of Results
1978	1
1979	2
1981	1
1983	2
1984	2
1985	1
1986	5
1987	1
1989	2
1991	2
1992	1
1998	1
1999	2
2008	1
2025	0

1

Mosaicism for a tandem duplication dup(1)(q12q22) in an 18 year old female.

de Silva D, Massie D, Drummond J, Couzin D, Dean JC. de Silva D, et al. Among authors: couzin d. J Med Genet. 1998 Jul;35(7):600-3. doi: 10.1136/jmg.35.7.600. J Med Genet. 1998. PMID: 9678707 Free PMC article. Review.

2

A fertile woman with non-mosaic Turner's syndrome. Case report and review of the literature.

Swapp GH, Johnston AW, Watt JL, Couzin DA, Stephen GS. Swapp GH, et al. Among authors: couzin da. Br J Obstet Gynaecol. 1989 Jul;96(7):876-80. doi: 10.1111/j.1471-0528.1989.tb03332.x. Br J Obstet Gynaecol. 1989. PMID: 2669936 Review. No abstract available.

3

Cystic fibrosis and chromosomal abnormalities.

Symon DN, Russell G, Couzin DA, Stewart L. Symon DN, et al. Among authors: couzin da. Lancet. 1984 May 12;1(8385):1070. doi: 10.1016/s0140-6736(84)91472-7. Lancet. 1984. PMID: 6143993 No abstract available.

4

Chromosome 22q11 microdeletion and congenital heart disease--a survey in a paediatric population.

Yong DE, Booth P, Baruni J, Massie D, Stephen G, Couzin D, Dean JC. Yong DE, et al. Among authors: couzin d. Eur J Pediatr. 1999 Jul;158(7):566-70. doi: 10.1007/s004310051148. Eur J Pediatr. 1999. PMID: 10412816

5

Mortality in women with turner syndrome in Great Britain: a national cohort study.

Schoemaker MJ, Swerdlow AJ, Higgins CD, Wright AF, Jacobs PA; United Kingdom Clinical Cytogenetics Group. Schoemaker MJ, et al. J Clin Endocrinol Metab. 2008 Dec;93(12):4735-42. doi: 10.1210/jc.2008-1049. Epub 2008 Sep 23. J Clin Endocrinol Metab. 2008. PMID: 18812477

6

Structural rearrangements in the parents of children with primary trisomy 21.

Couzin DA, Watt JL, Stephen GS. Couzin DA, et al. J Med Genet. 1987 May;24(5):280-2. doi: 10.1136/jmg.24.5.280. J Med Genet. 1987. PMID: 2953898 Free PMC article.

7

A familial pericentric inversion of chromosome 22 with a recombinant subject illustrating a 'pure' partial monosomy syndrome.

Watt JL, Olson IA, Johnston AW, Ross HS, Couzin DA, Stephen GS. Watt JL, et al. Among authors: couzin da. J Med Genet. 1985 Aug;22(4):283-7. doi: 10.1136/jmg.22.4.283. J Med Genet. 1985. PMID: 4045954 Free PMC article.

8

Prenatal detection of Turner's syndrome in conjunction with trisomy 20 mosaicism (45,X/46, X, +0).

Watt JL, Couzin DA, Johnston AW, Jandial V, Gray ES. Watt JL, et al. Among authors: couzin da. J Med Genet. 1981 Jun;18(3):225-7. doi: 10.1136/jmg.18.3.225. J Med Genet. 1981. PMID: 7241546 Free PMC article.

9

Ectrodactyly-mandibulo-facial dysostosis: case report and delineation of an entity.

Turnpenny PD, Johnston AW, Dean JC, Haites NE, Couzin DA, Stephen GS. Turnpenny PD, et al. Among authors: couzin da. Clin Dysmorphol. 1992 Apr;1(2):103-9. Clin Dysmorphol. 1992. PMID: 1345512 Review.

10

Prenatal diagnosis of a case of 46,XY,18p-/46,XY,18p+ mosaicism.

Stephen GS, Couzin DA, Watt JL, Rankin R. Stephen GS, et al. Among authors: couzin da. Prenat Diagn. 1989 Jan;9(1):57-60. doi: 10.1002/pd.1970090108. Prenat Diagn. 1989. PMID: 2748551

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Results by year

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

24 results

Results by year

Search Page

Filters

My Custom Filters

Results by year

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

24 results

Results by year