Wessels MW - Search Results

1

Phenotypic variability of atypical 22q11.2 deletions not including TBX1.

Verhagen JM, Diderich KE, Oudesluijs G, Mancini GM, Eggink AJ, Verkleij-Hagoort AC, Groenenberg IA, Willems PJ, du Plessis FA, de Man SA, Srebniak MI, van Opstal D, Hulsman LO, van Zutven LJ, Wessels MW. Verhagen JM, et al. Among authors: wessels mw. Am J Med Genet A. 2012 Oct;158A(10):2412-20. doi: 10.1002/ajmg.a.35517. Epub 2012 Aug 14. Am J Med Genet A. 2012. PMID: 22893440

2

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.

3

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

4

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.

5

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.

6

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

7

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

8

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.

9

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

10

Prenatal diagnosis of boomerang dysplasia.

Wessels MW, Den Hollander NS, De Krijger RR, Bonifé L, Superti-Furga A, Nikkels PG, Willems PJ. Wessels MW, et al. Am J Med Genet A. 2003 Oct 1;122A(2):148-54. doi: 10.1002/ajmg.a.20239. Am J Med Genet A. 2003. PMID: 12955767

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