Marynen P - Search Results

1

Localisation of a new gene for non-specific mental retardation to Xq22-q26 (MRX35).

Gu XX, Decorte R, Marynen P, Fryns JP, Cassiman JJ, Raeymaekers P. Gu XX, et al. Among authors: marynen p. J Med Genet. 1996 Jan;33(1):52-5. doi: 10.1136/jmg.33.1.52. J Med Genet. 1996. PMID: 8825049 Free PMC article.

2

Clinical study and haplotype analysis in two brothers with Partington syndrome.

Frints SG, Borghgraef M, Froyen G, Marynen P, Fryns JP. Frints SG, et al. Among authors: marynen p. Am J Med Genet. 2002 Nov 1;112(4):361-8. doi: 10.1002/ajmg.10630. Am J Med Genet. 2002. PMID: 12376938

3

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: marynen p. 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.

4

Encephalocraniocutaneous lipomatosis with a mutation in the NF1 gene.

Legius E, Wu R, Eyssen M, Marynen P, Fryns JP, Cassiman JJ. Legius E, et al. Among authors: marynen p. J Med Genet. 1995 Apr;32(4):316-9. doi: 10.1136/jmg.32.4.316. J Med Genet. 1995. PMID: 7643367 Free PMC article.

5

Genetic heterogeneity in Rieger eye malformation.

Legius E, de Die-Smulders CE, Verbraak F, Habex H, Decorte R, Marynen P, Fryns JP, Cassiman JJ. Legius E, et al. Among authors: marynen p. J Med Genet. 1994 Apr;31(4):340-1. doi: 10.1136/jmg.31.4.340. J Med Genet. 1994. PMID: 8071964 Free PMC article.

6

Identification of internal variation in the pseudoautosomal VNTR DXYS17, with nonrandom distribution of the alleles on the X and the Y chromosomes.

Decorte R, Wu R, Marynen P, Cassiman JJ. Decorte R, et al. Among authors: marynen p. Am J Hum Genet. 1994 Mar;54(3):506-15. Am J Hum Genet. 1994. PMID: 8116620 Free PMC article.

7

Linkage analysis in three families with nonspecific X-linked mental retardation.

Claes S, Gu XX, Legius E, Lorenzetti E, Marynen P, Fryns JP, Cassiman JJ, Raeymaekers P. Claes S, et al. Among authors: marynen p. Am J Med Genet. 1996 Jul 12;64(1):137-46. doi: 10.1002/(SICI)1096-8628(19960712)64:1<137::AID-AJMG24>3.0.CO;2-N. Am J Med Genet. 1996. PMID: 8826464

8

Trisomy 15 rescue with jumping translocation of distal 15q in Prader-Willi syndrome.

Devriendt K, Petit P, Matthijs G, Vermeesch JR, Holvoet M, De Muelenaere A, Marynen P, Cassiman JJ, Fryns JP. Devriendt K, et al. Among authors: marynen p. J Med Genet. 1997 May;34(5):395-9. doi: 10.1136/jmg.34.5.395. J Med Genet. 1997. PMID: 9152837 Free PMC article.

9

Emerging patterns of cryptic chromosomal imbalance in patients with idiopathic mental retardation and multiple congenital anomalies: a new series of 140 patients and review of published reports.

Menten B, Maas N, Thienpont B, Buysse K, Vandesompele J, Melotte C, de Ravel T, Van Vooren S, Balikova I, Backx L, Janssens S, De Paepe A, De Moor B, Moreau Y, Marynen P, Fryns JP, Mortier G, Devriendt K, Speleman F, Vermeesch JR. Menten B, et al. Among authors: marynen p. J Med Genet. 2006 Aug;43(8):625-33. doi: 10.1136/jmg.2005.039453. Epub 2006 Feb 20. J Med Genet. 2006. PMID: 16490798 Free PMC article.

10

Detection of genomic copy number changes in patients with idiopathic mental retardation by high-resolution X-array-CGH: important role for increased gene dosage of XLMR genes.

Froyen G, Van Esch H, Bauters M, Hollanders K, Frints SG, Vermeesch JR, Devriendt K, Fryns JP, Marynen P. Froyen G, et al. Among authors: marynen p. Hum Mutat. 2007 Oct;28(10):1034-42. doi: 10.1002/humu.20564. Hum Mutat. 2007. PMID: 17546640

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