Legius E - Search Results

1

Presymptomatic Identification of Cancers in Pregnant Women During Noninvasive Prenatal Testing.

Amant F, Verheecke M, Wlodarska I, Dehaspe L, Brady P, Brison N, Van Den Bogaert K, Dierickx D, Vandecaveye V, Tousseyn T, Moerman P, Vanderstichele A, Vergote I, Neven P, Berteloot P, Putseys K, Danneels L, Vandenberghe P, Legius E, Vermeesch JR. Amant F, et al. Among authors: legius e. JAMA Oncol. 2015 Sep;1(6):814-9. doi: 10.1001/jamaoncol.2015.1883. JAMA Oncol. 2015. PMID: 26355862

2

Holzgreve-Wagner-Rehder syndrome: Potter sequence associated with persistent buccopharyngeal membrane. A second observation.

Legius E, Moerman P, Fryns JP, Vandenberghe K, Eggermont E. Legius E, et al. Am J Med Genet. 1988 Oct;31(2):269-72. doi: 10.1002/ajmg.1320310203. Am J Med Genet. 1988. PMID: 3232694

3

Catel-Manzke palatodigital syndrome in a second trimester female foetus with nuchal oedema, costovertebral anomalies and radial ray defect.

Petit P, Moerman P, Legius E, Fryns JP. Petit P, et al. Among authors: legius e. Genet Couns. 1994;5(4):381-5. Genet Couns. 1994. PMID: 7888142

4

Apparently new "anophthalmia-plus" syndrome in sibs.

Fryns JP, Legius E, Moerman P, Vandenberghe K, Van den Berghe H. Fryns JP, et al. Among authors: legius e. Am J Med Genet. 1995 Aug 28;58(2):113-4. doi: 10.1002/ajmg.1320580204. Am J Med Genet. 1995. PMID: 8533799

5

De novo 46,XX, dir dup (11)(q133.3-->q14.2) in a patient with mental retardation, congenital cardiopathy and thrombopenia.

Legius E, Wlodarska I, Selleri L, Evans GA, Wu R, Smet G, Fryns JP. Legius E, et al. Clin Genet. 1996 Apr;49(4):206-10. doi: 10.1111/j.1399-0004.1996.tb03288.x. Clin Genet. 1996. PMID: 8828987

6

Associated malformations and chromosomal anomalies in 42 cases of prenatally diagnosed diaphragmatic hernia.

Witters I, Legius E, Moerman P, Deprest J, Van Schoubroeck D, Timmerman D, Van Assche FA, Fryns JP. Witters I, et al. Among authors: legius e. Am J Med Genet. 2001 Nov 1;103(4):278-82. Am J Med Genet. 2001. PMID: 11746006

7

Semilobar holoprosencephaly in a 46,XY female fetus.

Witters I, Moerman P, Muenke M, Van Assche FA, Devriendt K, Legius E, Van Schoubroeck D, Fryns JP. Witters I, et al. Among authors: legius e. Prenat Diagn. 2001 Oct;21(10):839-41. doi: 10.1002/pd.151. Prenat Diagn. 2001. PMID: 11746125

8

Genomic organization and evolution of the NF1 microdeletion region.

De Raedt T, Brems H, Lopez-Correa C, Vermeesch JR, Marynen P, Legius E. De Raedt T, et al. Among authors: legius e. Genomics. 2004 Aug;84(2):346-60. doi: 10.1016/j.ygeno.2004.03.006. Genomics. 2004. PMID: 15233998

9

Large deletions of the APC gene in 15% of mutation-negative patients with classical polyposis (FAP): a Belgian study.

Michils G, Tejpar S, Thoelen R, van Cutsem E, Vermeesch JR, Fryns JP, Legius E, Matthijs G. Michils G, et al. Among authors: legius e. Hum Mutat. 2005 Feb;25(2):125-34. doi: 10.1002/humu.20122. Hum Mutat. 2005. PMID: 15643602

10

Prophylactic salpingo-oophorectomy in 51 women with familial breast-ovarian cancer: importance of fallopian tube dysplasia.

Leunen K, Legius E, Moerman P, Amant F, Neven P, Vergote I. Leunen K, et al. Among authors: legius e. Int J Gynecol Cancer. 2006 Jan-Feb;16(1):183-8. doi: 10.1111/j.1525-1438.2006.00287.x. Int J Gynecol Cancer. 2006. PMID: 16445631

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

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

332 results

Search Page

Filters