Holvoet M - Search Results

1

X-linked mental retardation, short stature, microcephaly and hypogonadism maps to Xp22.1-p21.3 in a Belgian family.

Van Esch H, Zanni G, Holvoet M, Borghgraef M, Chelly J, Fryns JP, Devriendt K. Van Esch H, et al. Among authors: holvoet m. Eur J Med Genet. 2005 Apr-Jun;48(2):145-52. doi: 10.1016/j.ejmg.2005.01.016. Epub 2005 Feb 12. Eur J Med Genet. 2005. PMID: 16053905

2

HUWE1 mutation explains phenotypic severity in a case of familial idiopathic intellectual disability.

Isrie M, Kalscheuer VM, Holvoet M, Fieremans N, Van Esch H, Devriendt K. Isrie M, et al. Among authors: holvoet m. Eur J Med Genet. 2013 Jul;56(7):379-82. doi: 10.1016/j.ejmg.2013.05.005. Epub 2013 May 27. Eur J Med Genet. 2013. PMID: 23721686

3

A recognisable behavioural phenotype associated with terminal deletions of the short arm of chromosome 8.

Claeys I, Holvoet M, Eyskens B, Adriaensens P, Gewillig M, Fryns JP, Devriendt K. Claeys I, et al. Among authors: holvoet m. Am J Med Genet. 1997 Sep 19;74(5):515-20. doi: 10.1002/(sici)1096-8628(19970919)74:5<515::aid-ajmg12>3.0.co;2-f. Am J Med Genet. 1997. PMID: 9342203

4

Regional localization of two genes for nonspecific X-linked mental retardation to Xp22.3-p22.2 (MRX49) and Xp11.3-p11.21 (MRX50).

Claes S, Vogels A, Holvoet M, Devriendt K, Raeymaekers P, Cassiman JJ, Fryns JP. Claes S, et al. Among authors: holvoet m. Am J Med Genet. 1997 Dec 31;73(4):474-9. Am J Med Genet. 1997. PMID: 9415477

5

Triplication of distal chromosome 10q.

Devriendt K, Matthijs G, Holvoet M, Schoenmakers E, Fryns JP. Devriendt K, et al. Among authors: holvoet m. J Med Genet. 1999 Mar;36(3):242-5. J Med Genet. 1999. PMID: 10204854 Free PMC article.

6

Regional localization of a gene for nonspecific XLMR to Xp11.3-p11. 23 (MRX51) and tentative localization of an MRX gene to Xq23-q26.1.

Claes S, Volcke P, Devriendt K, Holvoet M, Raeymaekers P, Cassiman JJ, Fryns JP. Claes S, et al. Among authors: holvoet m. Am J Med Genet. 1999 Jul 30;85(3):283-7. Am J Med Genet. 1999. PMID: 10398244

7

Glypican 1 gene: good candidate for brachydactyly type E.

Syrrou M, Keymolen K, Devriendt K, Holvoet M, Thoelen R, Verhofstadt K, Fryns JP. Syrrou M, et al. Among authors: holvoet m. Am J Med Genet. 2002 Apr 1;108(4):310-4. doi: 10.1002/ajmg.10266. Am J Med Genet. 2002. PMID: 11920836

8

The mitochondrial solute carrier SLC25A5 at Xq24 is a novel candidate gene for non-syndromic intellectual disability.

Vandewalle J, Bauters M, Van Esch H, Belet S, Verbeeck J, Fieremans N, Holvoet M, Vento J, Spreiz A, Kotzot D, Haberlandt E, Rosenfeld J, Andrieux J, Delobel B, Dehouck MB, Devriendt K, Fryns JP, Marynen P, Goldstein A, Froyen G. Vandewalle J, et al. Among authors: holvoet m. Hum Genet. 2013 Oct;132(10):1177-85. doi: 10.1007/s00439-013-1322-3. Epub 2013 Jun 20. Hum Genet. 2013. PMID: 23783460

9

Genotype-phenotype correlations of UBA2 mutations in patients with ectrodactyly.

Aerden M, Bauters M, Van Den Bogaert K, Vermeesch JR, Holvoet M, Plasschaert F, Devriendt K. Aerden M, et al. Among authors: holvoet m. Eur J Med Genet. 2020 Nov;63(11):104009. doi: 10.1016/j.ejmg.2020.104009. Epub 2020 Aug 3. Eur J Med Genet. 2020. PMID: 32758660

10

A clinical, cytogenetic and familial study of 307 mentally retarded, institutionalized, adult male patients with special interest for fra(X) negative X-linked mental retardation.

Haspeslagh M, Fryns JP, Holvoet M, Collen G, Dierck G, Baeke J, van den Berghe H. Haspeslagh M, et al. Among authors: holvoet m. Clin Genet. 1991 Jun;39(6):434-41. doi: 10.1111/j.1399-0004.1991.tb03055.x. Clin Genet. 1991. PMID: 1863991

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