Peeters H - Search Results

1

Facial dysmorphism is influenced by ethnic background of the patient and of the evaluator.

Lumaka A, Cosemans N, Lulebo Mampasi A, Mubungu G, Mvuama N, Lubala T, Mbuyi-Musanzayi S, Breckpot J, Holvoet M, de Ravel T, Van Buggenhout G, Peeters H, Donnai D, Mutesa L, Verloes A, Lukusa Tshilobo P, Devriendt K. Lumaka A, et al. Among authors: peeters h. Clin Genet. 2017 Aug;92(2):166-171. doi: 10.1111/cge.12948. Epub 2017 Jan 16. Clin Genet. 2017. PMID: 27925162

2

Recurrent involvement of chromosomal region 6q21 in heterotaxy.

Peeters H, Debeer P, Groenen P, Van Esch H, Vanderlinden G, Eyskens B, Mertens L, Gewillig M, Van de Ven W, Fryns JP, Devriendt K. Peeters H, et al. Am J Med Genet. 2001 Sep 15;103(1):44-7. doi: 10.1002/ajmg.1499. Am J Med Genet. 2001. PMID: 11562933

3

PA26 is a candidate gene for heterotaxia in humans: identification of a novel PA26-related gene family in human and mouse.

Peeters H, Debeer P, Bairoch A, Wilquet V, Huysmans C, Parthoens E, Fryns JP, Gewillig M, Nakamura Y, Niikawa N, Van de Ven W, Devriendt K. Peeters H, et al. Hum Genet. 2003 May;112(5-6):573-80. doi: 10.1007/s00439-003-0917-5. Epub 2003 Feb 27. Hum Genet. 2003. PMID: 12607115

4

Variable phenotype in Greig cephalopolysyndactyly syndrome: clinical and radiological findings in 4 independent families and 3 sporadic cases with identified GLI3 mutations.

Debeer P, Peeters H, Driess S, De Smet L, Freese K, Matthijs G, Bornholdt D, Devriendt K, Grzeschik KH, Fryns JP, Kalff-Suske M. Debeer P, et al. Among authors: peeters h. Am J Med Genet A. 2003 Jul 1;120A(1):49-58. doi: 10.1002/ajmg.a.20018. Am J Med Genet A. 2003. PMID: 12794692

5

Human laterality disorders.

Peeters H, Devriendt K. Peeters H, et al. Eur J Med Genet. 2006 Sep-Oct;49(5):349-62. doi: 10.1016/j.ejmg.2005.12.003. Epub 2006 Jan 3. Eur J Med Genet. 2006. PMID: 16461029 Review.

6

Focal preauricular dermal dysplasia: distinctive congenital lesions with a bilateral and symmetric distribution.

Prescott T, Devriendt K, Hamel B, Pasch MC, Peeters H, Vander Poorten V, Tallerås O. Prescott T, et al. Among authors: peeters h. Eur J Med Genet. 2006 Mar-Apr;49(2):135-9. doi: 10.1016/j.ejmg.2005.06.005. Epub 2005 Aug 11. Eur J Med Genet. 2006. PMID: 16530710 Review.

7

Two female siblings with congenital heart disease, postaxial polydactyly, ectopic neuropituitary gland, hair anomalies and characteristic facial features: a new syndrome?

Goossens L, Janssens S, Meersschaut V, Peeters H, Devlieger H, Devriendt K. Goossens L, et al. Among authors: peeters h. Clin Dysmorphol. 2006 Apr;15(2):71-4. doi: 10.1097/01.mcd.0000194409.30794.66. Clin Dysmorphol. 2006. PMID: 16531731

8

DISC1 duplication in two brothers with autism and mild mental retardation.

Crepel A, Breckpot J, Fryns JP, De la Marche W, Steyaert J, Devriendt K, Peeters H. Crepel A, et al. Among authors: peeters h. Clin Genet. 2010 Apr;77(4):389-94. doi: 10.1111/j.1399-0004.2009.01318.x. Epub 2009 Dec 10. Clin Genet. 2010. PMID: 20002455

9

Array comparative genomic hybridization as a diagnostic tool for syndromic heart defects.

Breckpot J, Thienpont B, Peeters H, de Ravel T, Singer A, Rayyan M, Allegaert K, Vanhole C, Eyskens B, Vermeesch JR, Gewillig M, Devriendt K. Breckpot J, et al. Among authors: peeters h. J Pediatr. 2010 May;156(5):810-7, 817.e1-817.e4. doi: 10.1016/j.jpeds.2009.11.049. Epub 2010 Feb 6. J Pediatr. 2010. PMID: 20138633

10

Microduplication 22q11.2: a description of the clinical, developmental and behavioral characteristics during childhood.

Van Campenhout S, Devriendt K, Breckpot J, Frijns JP, Peeters H, Van Buggenhout G, Van Esch H, Maes B, Swillen A. Van Campenhout S, et al. Among authors: peeters h. Genet Couns. 2012;23(2):135-48. Genet Couns. 2012. PMID: 22876571

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