Legius E - Search Results

1

Mutations in L1-CAM in two families with X linked complicated spastic paraplegia, MASA syndrome, and HSAS.

Ruiz JC, Cuppens H, Legius E, Fryns JP, Glover T, Marynen P, Cassiman JJ. Ruiz JC, et al. Among authors: legius e. J Med Genet. 1995 Jul;32(7):549-52. doi: 10.1136/jmg.32.7.549. J Med Genet. 1995. PMID: 7562969 Free PMC article.

2

NF1-related locus on chromosome 15.

Legius E, Marchuk DA, Hall BK, Andersen LB, Wallace MR, Collins FS, Glover TW. Legius E, et al. Genomics. 1992 Aug;13(4):1316-8. doi: 10.1016/0888-7543(92)90055-w. Genomics. 1992. PMID: 1505963 Free article.

3

MASA syndrome (a form of complicated spastic paraplegia) and X linked hydrocephalus: variable expression of the same mutation at Xq28? Call for families.

Schrander-Stumpel C, Fryns J, Cassiman JJ, Legius E, Spaepen A, Höweler CJ. Schrander-Stumpel C, et al. Among authors: legius e. J Med Genet. 1992 Mar;29(3):215. doi: 10.1136/jmg.29.3.215-a. J Med Genet. 1992. PMID: 1552562 Free PMC article. No abstract available.

4

A yeast artificial chromosome contig encompassing the type 1 neurofibromatosis gene.

Marchuk DA, Tavakkol R, Wallace MR, Brownstein BH, Taillon-Miller P, Fong CT, Legius E, Andersen LB, Glover TW, Collins FS. Marchuk DA, et al. Among authors: legius e. Genomics. 1992 Jul;13(3):672-80. doi: 10.1016/0888-7543(92)90140-n. Genomics. 1992. PMID: 1639394 Free article.

5

Molecular and cytogenetic analysis of tumors in von Recklinghausen neurofibromatosis.

Glover TW, Stein CK, Legius E, Andersen LB, Brereton A, Johnson S. Glover TW, et al. Among authors: legius e. Genes Chromosomes Cancer. 1991 Jan;3(1):62-70. doi: 10.1002/gcc.2870030111. Genes Chromosomes Cancer. 1991. PMID: 1906341

6

Opitz C syndrome and pseudohypoaldosteronism.

De Koster J, Legius E, de Zegher F, Devlieger H, Fryns JP, Eggermont E. De Koster J, et al. Among authors: legius e. Am J Med Genet. 1990 Dec;37(4):457-9. doi: 10.1002/ajmg.1320370405. Am J Med Genet. 1990. PMID: 2175542

7

Sporadic late onset ornithine transcarbamylase deficiency in a boy with somatic mosaicism for an intragenic deletion.

Legius E, Baten E, Stul M, Marynen P, Cassiman JJ. Legius E, et al. Clin Genet. 1990 Aug;38(2):155-9. doi: 10.1111/j.1399-0004.1990.tb03565.x. Clin Genet. 1990. PMID: 2208768

8

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

9

MASA syndrome: new clinical features and linkage analysis using DNA probes.

Schrander-Stumpel C, Legius E, Fryns JP, Cassiman JJ. Schrander-Stumpel C, et al. Among authors: legius e. J Med Genet. 1990 Nov;27(11):688-92. doi: 10.1136/jmg.27.11.688. J Med Genet. 1990. PMID: 2277384 Free PMC article.

10

EEC syndrome without ectrodactyly: report of two new families.

Fryns JP, Legius E, Dereymaeker AM, Van den Berghe H. Fryns JP, et al. Among authors: legius e. J Med Genet. 1990 Mar;27(3):165-8. doi: 10.1136/jmg.27.3.165. J Med Genet. 1990. PMID: 2325090 Free PMC article.

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