Wessels MW - Search Results

1

Phenotypic spectrum of the SMAD3-related aneurysms-osteoarthritis syndrome.

van de Laar IM, van der Linde D, Oei EH, Bos PK, Bessems JH, Bierma-Zeinstra SM, van Meer BL, Pals G, Oldenburg RA, Bekkers JA, Moelker A, de Graaf BM, Matyas G, Frohn-Mulder IM, Timmermans J, Hilhorst-Hofstee Y, Cobben JM, Bruggenwirth HT, van Laer L, Loeys B, De Backer J, Coucke PJ, Dietz HC, Willems PJ, Oostra BA, De Paepe A, Roos-Hesselink JW, Bertoli-Avella AM, Wessels MW. van de Laar IM, et al. Among authors: wessels mw. J Med Genet. 2012 Jan;49(1):47-57. doi: 10.1136/jmedgenet-2011-100382. J Med Genet. 2012. PMID: 22167769

2

In utero diagnosis of infra-diaphragmatic total anomalous pulmonary venous return.

Wessels MW, Frohn-Mulder IM, Cromme-Dijkhuis AH, Wladimiroff JW. Wessels MW, et al. Ultrasound Obstet Gynecol. 1996 Sep;8(3):206-9. doi: 10.1046/j.1469-0705.1996.08030206.x. Ultrasound Obstet Gynecol. 1996. PMID: 8915092 Free article.

3

Mutational spectrum of the TSC1 gene in a cohort of 225 tuberous sclerosis complex patients: no evidence for genotype-phenotype correlation.

van Slegtenhorst M, Verhoef S, Tempelaars A, Bakker L, Wang Q, Wessels M, Bakker R, Nellist M, Lindhout D, Halley D, van den Ouweland A. van Slegtenhorst M, et al. J Med Genet. 1999 Apr;36(4):285-9. J Med Genet. 1999. PMID: 10227394 Free PMC article.

4

Unexpected life-threatening complications in Kabuki syndrome.

van Haelst MM, Brooks AS, Hoogeboom J, Wessels MW, Tibboel D, de Jongste JC, den Hollander JC, Bongers-Schokking JJ, Niermeijer MF, Willems PJ. van Haelst MM, et al. Among authors: wessels mw. Am J Med Genet. 2000 Sep 11;94(2):170-3. doi: 10.1002/1096-8628(20000911)94:2<170::aid-ajmg10>3.0.co;2-2. Am J Med Genet. 2000. PMID: 10982974

5

Kabuki syndrome: a review study of three hundred patients.

Wessels MW, Brooks AS, Hoogeboom J, Niermeijer MF, Willems PJ. Wessels MW, et al. Clin Dysmorphol. 2002 Apr;11(2):95-102. doi: 10.1097/00019605-200204000-00004. Clin Dysmorphol. 2002. PMID: 12002156 Review.

6

Images in clinical medicine. Chondrodysplasia punctata.

Wessels MW, Willems PJ. Wessels MW, et al. N Engl J Med. 2002 Jul 11;347(2):110. doi: 10.1056/NEJMicm010895. N Engl J Med. 2002. PMID: 12110739 Free article. No abstract available.

7

Prenatal diagnosis and confirmation of the acrofacial dysostosis syndrome type Rodriguez.

Wessels MW, Den Hollander NS, Cohen-Overbeek TE, Lesnik Oberstein MS, Nash RM, Wladimiroff JW, Niermeijer MF, Willems PJ. Wessels MW, et al. Am J Med Genet. 2002 Nov 15;113(1):97-100. doi: 10.1002/ajmg.10729. Am J Med Genet. 2002. PMID: 12400073

8

Poor outcome in Down syndrome fetuses with cardiac anomalies or growth retardation.

Wessels MW, Los FJ, Frohn-Mulder IM, Niermeijer MF, Willems PJ, Wladimiroff JW. Wessels MW, et al. Am J Med Genet A. 2003 Jan 15;116A(2):147-51. doi: 10.1002/ajmg.a.10823. Am J Med Genet A. 2003. PMID: 12494433

9

Mild fetal cerebral ventriculomegaly as a prenatal sonographic marker for Kartagener syndrome.

Wessels MW, den Hollander NS, Willems PJ. Wessels MW, et al. Prenat Diagn. 2003 Mar;23(3):239-42. doi: 10.1002/pd.551. Prenat Diagn. 2003. PMID: 12627427 Free article.

10

Fetus with an unusual form of nonrhizomelic chondrodysplasia punctata: case report and review.

Wessels MW, Den Hollander NJ, De Krijger RR, Nikkels PG, Brandenburg H, Hennekam R, Willems PJ. Wessels MW, et al. Am J Med Genet A. 2003 Jul 1;120A(1):97-104. doi: 10.1002/ajmg.a.20202. Am J Med Genet A. 2003. PMID: 12794700

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