P J Willems
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Explore the profile of P J Willems including associated specialties, affiliations and a list of published articles.
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Articles
173
Citations
4260
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Recent Articles
1.
Hendrickx J, Wauters J, Coucke P, Vits L, Auwera B, Willems P
Acta Clin Belg
. 2016 Jul;
46(1):13-7.
PMID: 27369461
Cystic fibrosis (CF) is one of the most frequent recessive disorders among Caucasians. DNA analysis is perfonned by linkage analysis with DNA markers tightly linked to the CF gene. Cloning...
2.
Papadimitriou D, Willems P, Bothou C, Karpathios T, Papadimitriou A
Diabetes Metab
. 2015 Apr;
41(4):342-343.
PMID: 25921421
No abstract available.
3.
Bevilacqua E, Gil M, Nicolaides K, Ordonez E, Cirigliano V, Dierickx H, et al.
Ultrasound Obstet Gynecol
. 2014 Oct;
45(1):61-6.
PMID: 25297464
Objectives: To report clinical implementation of cell-free DNA (cfDNA) analysis of maternal blood in screening for trisomies 21, 18 and 13 in twin pregnancies and examine variables that could influence...
4.
Willems P, Dierickx H, Vandenakker E, Bekedam D, Segers N, Deboulle K, et al.
Facts Views Vis Obgyn
. 2014 Jul;
6(1):7-12.
PMID: 25009720
As the classical first trimester Down syndrome screening (FTS, combination test) has a false-negative rate of 20-25% and > 95% of the abnormal FTS results are false-positive, we evaluated the...
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6.
Wessels M, Willems P
Clin Genet
. 2010 May;
78(2):103-23.
PMID: 20497191
The genetic defect in most patients with non-syndromic congenital heart malformations (CHM) is unknown, although more than 40 different genes have already been implicated. Only a minority of CHM seems...
7.
Petersen M, Wang Q, Willems P
Clin Genet
. 2007 Nov;
73(1):14-23.
PMID: 18005182
Many human syndromes associated with hearing loss are caused by disease genes located on the X chromosome, but few X-linked loci for non-syndromic hearing loss have been reported. Surprisingly, a...
8.
9.
Kokotas H, Petersen M, Willems P
Clin Genet
. 2007 May;
71(5):379-91.
PMID: 17489842
Non-syndromic deafness can be caused by mutations in both nuclear and mitochondrial genes. More than 50 nuclear genes have been shown to be involved in non-syndromic hearing loss, but mutations...
10.
Brooks A, Leegwater P, Burzynski G, Willems P, de Graaf B, van Langen I, et al.
J Med Genet
. 2006 Jul;
43(7):e35.
PMID: 16816022
We report on a multigenerational family with isolated Hirschsprung's disease (HSCR). Five patients were affected by either short segment or long segment HSCR. The family consists of two main branches:...