Similar articles for PMID: 12599193

Year	Number of Results
1990	1
1992	3
1993	2
1994	2
1995	1
1996	4
1997	6
1998	2
1999	1
2000	2
2001	2
2002	7
2003	13
2004	3
2005	6
2006	5
2007	2
2008	1
2009	6
2011	3
2012	4
2014	5
2015	3
2016	4
2017	5
2018	2
2019	6
2020	1
2024	0

1

Prenatal diagnosis of mosaic tetrasomy 10p associated with megacisterna magna, echogenic focus of left ventricle, umbilical cord cysts and distal arthrogryposis.

Wu YC, Yu MT, Chen LC, Chen CL, Yang ML. Wu YC, et al. Am J Med Genet A. 2003 Mar 15;117A(3):278-81. doi: 10.1002/ajmg.a.10007. Am J Med Genet A. 2003. PMID: 12599193

2

Prenatal diagnosis of occipital encephalocele, mega-cisterna magna, mesomelic shortening, and clubfeet associated with pure tetrasomy 20p.

Wu YC, Fang JS, Lee KF, Estipona J, Yang ML, Yuan CC. Wu YC, et al. Prenat Diagn. 2003 Feb;23(2):124-7. doi: 10.1002/pd.543. Prenat Diagn. 2003. PMID: 12575018

3

Prenatal management of mosaic tetrasomy 5p.

Reddy KS, Huang B. Reddy KS, et al. Prenat Diagn. 2003 Jan;23(1):82-5. doi: 10.1002/pd.510. Prenat Diagn. 2003. PMID: 12533823 No abstract available.

4

Prenatal diagnosis of mosaic ring chromosome 22 associated with cardiovascular abnormalities and intrauterine growth restriction.

Chen CP, Chern SR, Chang TY, Lee CC, Chen LF, Tzen CY, Wang W, Lin CJ, Yang BP, Yang LS. Chen CP, et al. Prenat Diagn. 2003 Jan;23(1):40-3. doi: 10.1002/pd.517. Prenat Diagn. 2003. PMID: 12533811

5

Mosaic "tetrasomy" 8p: case report and review of the literature.

Winters J, Markello T, Nance W, Jackson-Cook C. Winters J, et al. Clin Genet. 1995 Oct;48(4):195-8. doi: 10.1111/j.1399-0004.1995.tb04088.x. Clin Genet. 1995. PMID: 8591671 Review.

6

Prenatal detection of mosaic isochromosome 20q: a fourth report with abnormal phenotype.

Goumy C, Beaufrère AM, Francannet C, Tchirkov A, Laurichesse Delmas H, Geissler F, Lemery D, Dechelotte PJ, Vago P. Goumy C, et al. Prenat Diagn. 2005 Aug;25(8):653-5. doi: 10.1002/pd.1216. Prenat Diagn. 2005. PMID: 16049989

7

Diagnosis and clinical delineation of mosaic tetrasomy 5p.

Blakey-Cheung S, Parker P, Schlaff W, Monseur B, Keppler-Noreuil K, Al-Kouatly HB. Blakey-Cheung S, et al. Eur J Med Genet. 2020 Jan;63(1):103634. doi: 10.1016/j.ejmg.2019.02.006. Epub 2019 Feb 21. Eur J Med Genet. 2020. PMID: 30797979 Review.

8

Prenatal molecular cytogenetic diagnosis of partial tetrasomy 10p due to neocentromere formation in an inversion duplication analphoid marker chromosome.

Levy B, Papenhausen P, Tepperberg J, Dunn T, Fallet S, Magid M, Kardon N, Hirschhorn K, Warburton P. Levy B, et al. Cytogenet Cell Genet. 2000;91(1-4):165-70. doi: 10.1159/000056839. Cytogenet Cell Genet. 2000. PMID: 11173851

9

New case of non-mosaic tetrasomy 9p in a severely polymalformed newborn girl.

de Azevedo Moreira LM, Freitas LM, Gusmão FA, Riegel M. de Azevedo Moreira LM, et al. Birth Defects Res A Clin Mol Teratol. 2003 Dec;67(12):985-8. doi: 10.1002/bdra.10126. Birth Defects Res A Clin Mol Teratol. 2003. PMID: 14745919

10

Tetrasomy 12p--unusual presentation in CVS.

Dong L, Falk RE, Williams J 3rd, Kohan M, Schreck RR. Dong L, et al. Prenat Diagn. 2003 Feb;23(2):101-3. doi: 10.1002/pd.538. Prenat Diagn. 2003. PMID: 12575013

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 NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

99 results

Results by year