Legius E - Search Results

1

Chromosome 22q12.1 microdeletions: confirmation of the MN1 gene as a candidate gene for cleft palate.

Breckpot J, Anderlid BM, Alanay Y, Blyth M, Brahimi A, Duban-Bedu B, Gozé O, Firth H, Yakicier MC, Hens G, Rayyan M, Legius E, Vermeesch JR, Devriendt K. Breckpot J, et al. Among authors: legius e. Eur J Hum Genet. 2016 Jan;24(1):51-8. doi: 10.1038/ejhg.2015.65. Epub 2015 May 6. Eur J Hum Genet. 2016. PMID: 25944382 Free PMC article.

2

Association between XV2c/CS7/KM19/D9 haplotypes and the delta F508 mutation. A study of 57 Belgian families.

Cuppens H, Legius E, Cabello P, Marynen P, De Boeck C, Decorte R, Fryns JP, Eggermont E, Van den Berghe H, Cassiman JJ. Cuppens H, et al. Among authors: legius e. Hum Genet. 1990 Sep;85(4):402-3. doi: 10.1007/BF02428277. Hum Genet. 1990. PMID: 2210747

3

Diaphragmatic hernia in Denys-Drash syndrome.

Devriendt K, Deloof E, Moerman P, Legius E, Vanhole C, de Zegher F, Proesmans W, Devlieger H. Devriendt K, et al. Among authors: legius e. Am J Med Genet. 1995 May 22;57(1):97-101. doi: 10.1002/ajmg.1320570120. Am J Med Genet. 1995. PMID: 7645607

4

Limited expansion of the (CAG)n repeat of the Huntington gene: a premutation (?).

Legius E, Cuppens H, Dierick H, Van Zandt K, Dom R, Fryns JP, Evers-Kiebooms G, Decruyenaere M, Demyttenaere K, Marynen P, et al. Legius E, et al. Eur J Hum Genet. 1994;2(1):44-50. doi: 10.1159/000472340. Eur J Hum Genet. 1994. PMID: 8044653

5

Progressive extrapyramidal disorder with primary hypogonadism and alopecia in sibs: a new syndrome?

Devriendt K, Legius E, Fryns JP. Devriendt K, et al. Among authors: legius e. Am J Med Genet. 1996 Mar 1;62(1):54-7. doi: 10.1002/(SICI)1096-8628(19960301)62:1<54::AID-AJMG11>3.0.CO;2-U. Am J Med Genet. 1996. PMID: 8779325

6

Unusual molecular findings in autosomal recessive spinal muscular atrophy.

Matthijs G, Schollen E, Legius E, Devriendt K, Goemans N, Kayserili H, Apäk MY, Cassiman JJ. Matthijs G, et al. Among authors: legius e. J Med Genet. 1996 Jun;33(6):469-74. doi: 10.1136/jmg.33.6.469. J Med Genet. 1996. PMID: 8782046 Free PMC article.

7

Cohen syndrome: the clinical symptoms and stigmata at a young age.

Fryns JP, Legius E, Devriendt K, Meire F, Standaert L, Baten E, Van den Berghe H. Fryns JP, et al. Among authors: legius e. Clin Genet. 1996 May;49(5):237-41. doi: 10.1111/j.1399-0004.1996.tb03780.x. Clin Genet. 1996. PMID: 8832131

8

Skewed X-chromosome inactivation in female carriers of dyskeratosis congenita.

Devriendt K, Matthijs G, Legius E, Schollen E, Blockmans D, van Geet C, Degreef H, Cassiman JJ, Fryns JP. Devriendt K, et al. Among authors: legius e. Am J Hum Genet. 1997 Mar;60(3):581-7. Am J Hum Genet. 1997. PMID: 9042917 Free PMC article.

9

Prader-Willi syndrome in a child with mosaic trisomy 15 and mosaic triplo-X: a molecular analysis.

Devriendt K, Matthijs G, Claes S, Legius E, Proesmans W, Cassiman JJ, Fryns JP. Devriendt K, et al. Among authors: legius e. J Med Genet. 1997 Apr;34(4):318-22. doi: 10.1136/jmg.34.4.318. J Med Genet. 1997. PMID: 9138157 Free PMC article.

10

Intelligence and psychosocial adjustment in velocardiofacial syndrome: a study of 37 children and adolescents with VCFS.

Swillen A, Devriendt K, Legius E, Eyskens B, Dumoulin M, Gewillig M, Fryns JP. Swillen A, et al. Among authors: legius e. J Med Genet. 1997 Jun;34(6):453-8. doi: 10.1136/jmg.34.6.453. J Med Genet. 1997. PMID: 9192263 Free PMC article.

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