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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1987 2
1988 2
1989 2
1990 4
1991 5
1992 6
1993 2
1994 6
1995 1
1996 4
1998 1
1999 1
2000 2
2001 1
2002 4
2003 3
2005 2
2009 1
2014 1
2015 1
2024 0

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51 results

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Page 1
Autism spectrum disorder profile in neurofibromatosis type I.
Garg S, Plasschaert E, Descheemaeker MJ, Huson S, Borghgraef M, Vogels A, Evans DG, Legius E, Green J. Garg S, et al. Among authors: borghgraef m. J Autism Dev Disord. 2015 Jun;45(6):1649-57. doi: 10.1007/s10803-014-2321-5. J Autism Dev Disord. 2015. PMID: 25475362
Mosaic tetrasomy 8p in two patients: clinical data and review of the literature.
Schrander-Stumpel CT, Govaerts LC, Engelen JJ, van der Blij-Philipsen M, Borghgraef M, Loots WJ, Peters JJ, Rijnvos WP, Smeets DF, Fryns JP. Schrander-Stumpel CT, et al. Among authors: borghgraef m. Am J Med Genet. 1994 May 1;50(4):377-80. doi: 10.1002/ajmg.1320500416. Am J Med Genet. 1994. PMID: 7516121 Review.
Adults with Williams syndrome.
Fryns JP, Borghgraef M, Volcke P, Van den Berghe H. Fryns JP, et al. Among authors: borghgraef m. Am J Med Genet. 1991 Aug 1;40(2):253. doi: 10.1002/ajmg.1320400228. Am J Med Genet. 1991. PMID: 1897583 No abstract available.
A third MRX family (MRX68) is the result of mutation in the long chain fatty acid-CoA ligase 4 (FACL4) gene: proposal of a rapid enzymatic assay for screening mentally retarded patients.
Longo I, Frints SG, Fryns JP, Meloni I, Pescucci C, Ariani F, Borghgraef M, Raynaud M, Marynen P, Schwartz C, Renieri A, Froyen G. Longo I, et al. Among authors: borghgraef m. J Med Genet. 2003 Jan;40(1):11-7. doi: 10.1136/jmg.40.1.11. J Med Genet. 2003. PMID: 12525535 Free PMC article.
Seventh International Workshop on the Fragile X and X-linked Mental Retardation.
Tranebjaerg L, Lubs HA, Borghgraef M, Brown WT, Fisch G, Fryns JP, Hagerman R, Jacobs PA, Mandel JL, Mulley J, Oostra B, Schwartz C, Sherman S, Willard H, Willems P. Tranebjaerg L, et al. Among authors: borghgraef m. Am J Med Genet. 1996 Jul 12;64(1):1-14. doi: 10.1002/(SICI)1096-8628(19960712)64:1<1::AID-AJMG1>3.0.CO;2-Z. Am J Med Genet. 1996. PMID: 8826442 No abstract available.
51 results