Courtens W - Search Results

1

Further evidence for autosomal dominant inheritance and ectodermal abnormalities in Kabuki syndrome.

Courtens W, Rassart A, Stene JJ, Vamos E. Courtens W, et al. Am J Med Genet. 2000 Jul 31;93(3):244-9. doi: 10.1002/1096-8628(20000731)93:3<244::aid-ajmg17>3.0.co;2-2. Am J Med Genet. 2000. PMID: 10925391

2

Acrocallosal syndrome in an Algerian boy born to consanguineous parents: review of the literature and further delineation of the syndrome.

Courtens W, Vamos E, Christophe C, Schinzel A. Courtens W, et al. Am J Med Genet. 1997 Mar 3;69(1):17-22. doi: 10.1002/(sici)1096-8628(19970303)69:1<17::aid-ajmg4>3.0.co;2-q. Am J Med Genet. 1997. PMID: 9066878

3

Interstitial deletion 2q33.3-q34 in a boy with a phenotype resembling the Seckel syndrome.

Courtens W, Speleman F, Messiaen L, Bormans J, Van Roy N, Vamos E. Courtens W, et al. Am J Med Genet. 1997 Sep 5;71(4):479-85. Am J Med Genet. 1997. PMID: 9286460 Review.

4

Feingold syndrome: report of a new family and review.

Courtens W, Levi S, Verbelen F, Verloes A, Vamos E. Courtens W, et al. Am J Med Genet. 1997 Nov 28;73(1):55-60. Am J Med Genet. 1997. PMID: 9375923 Review.

5

Prenatal diagnosis of a constitutional interstitial deletion of chromosome 5 (q15q31.1) presenting with features of congenital contractural arachnodactyly.

Courtens W, Tjalma W, Messiaen L, Vamos E, Martin JJ, Van Bogaert E, Keersmaekers G, Meulyzer P, Wauters J. Courtens W, et al. Am J Med Genet. 1998 May 18;77(3):188-97. Am J Med Genet. 1998. PMID: 9605585

6

New syndrome or severe expression of Gordon syndrome? A case report.

Courtens W, Perlmutter N, Dan B, Vamos E. Courtens W, et al. Clin Dysmorphol. 1997 Jan;6(1):39-44. Clin Dysmorphol. 1997. PMID: 9018417

7

A probable case of Wiedemann-Rautenstrauch syndrome or neonatal progeroid syndrome and review of the literature.

Courtens W, Nuytinck L, Fricx C, André J, Vamos E. Courtens W, et al. Clin Dysmorphol. 1997 Jul;6(3):219-27. doi: 10.1097/00019605-199707000-00004. Clin Dysmorphol. 1997. PMID: 9220191 Review.

8

Noonan-like phenotype in monozygotic twins with a duplication-deficiency of the long arm of chromosome 18 resulting from a maternal paracentric inversion.

Courtens W, Grossman D, Van Roy N, Messiaen L, Vamos E, Toppet V, Haumont D, Streydio C, Jauch A, Vermeesch JR, Speleman F. Courtens W, et al. Hum Genet. 1998 Oct;103(4):497-505. doi: 10.1007/s004390050857. Hum Genet. 1998. PMID: 9856497

9

Unilateral bowing of long bones and multiple congenital anomalies in a child born to a mother with gestational diabetes.

Courtens W, De laet C, Ziereisen F, Vamos E, Mortier G. Courtens W, et al. Ann Genet. 2000 Apr-Jun;43(2):81-8. doi: 10.1016/s0003-3995(00)01020-0. Ann Genet. 2000. PMID: 10998449

10

CHARGE association in a neonate exposed in utero to carbon monoxide.

Courtens W, Hennequin Y, Blum D, Vamos E. Courtens W, et al. Birth Defects Orig Artic Ser. 1996;30(1):407-12. Birth Defects Orig Artic Ser. 1996. PMID: 9125346 No abstract available.

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