Witters I - Search Results

1

MCA syndrome with renal-hepatic-pancreatic dysplasia, posterior fossa cyst, symmetrical limb deficiencies, cleft palate, cardiac and Müllerian duct anomalies.

Witters I, Devriendt K, Spinnewijn D, Moerman P, Van Assche FA, Fryns JP. Witters I, et al. Am J Med Genet. 2002 Jan 22;107(3):233-6. doi: 10.1002/ajmg.10131. Am J Med Genet. 2002. PMID: 11807905

2

Fetal akinesia deformation sequence: a study of 30 consecutive in utero diagnoses.

Witters I, Moerman P, Fryns JP. Witters I, et al. Am J Med Genet. 2002 Nov 15;113(1):23-8. doi: 10.1002/ajmg.10698. Am J Med Genet. 2002. PMID: 12400062

3

Prenatal echographic diagnosis of laryngeal atresia as part of a multiple congenital anomalies (MCA) syndrome.

Witters I, Moerman P, Fryns JP. Witters I, et al. Genet Couns. 2000;11(3):215-9. Genet Couns. 2000. PMID: 11043429

4

Associated malformations and chromosomal anomalies in 42 cases of prenatally diagnosed diaphragmatic hernia.

Witters I, Legius E, Moerman P, Deprest J, Van Schoubroeck D, Timmerman D, Van Assche FA, Fryns JP. Witters I, et al. Am J Med Genet. 2001 Nov 1;103(4):278-82. Am J Med Genet. 2001. PMID: 11746006

5

Semilobar holoprosencephaly in a 46,XY female fetus.

Witters I, Moerman P, Muenke M, Van Assche FA, Devriendt K, Legius E, Van Schoubroeck D, Fryns JP. Witters I, et al. Prenat Diagn. 2001 Oct;21(10):839-41. doi: 10.1002/pd.151. Prenat Diagn. 2001. PMID: 11746125

6

Bilateral tibial agenesis with ectrodactyly (OMIM 119100): further evidence for autosomal recessive inheritance.

Witters I, Devriendt K, Moerman P, Caudron J, Van Hole C, Fryns JP. Witters I, et al. Am J Med Genet. 2001 Dec 1;104(3):209-13. Am J Med Genet. 2001. PMID: 11754046

7

Two siblings with early onset fetal akinesia deformation sequence and hydranencephaly: further evidence for autosomal recessive inheritance of hydranencephaly, fowler type.

Witters I, Moerman P, Devriendt K, Braet P, Van Schoubroeck D, Van Assche FA, Fryns JP. Witters I, et al. Am J Med Genet. 2002 Feb 15;108(1):41-4. Am J Med Genet. 2002. PMID: 11857548

8

Multiple congenital anomalies syndrome with multicystic renal dysplasia, postaxial polydactyly and lumbosacral meningocoele. Difficulties in nosological classification and genetic counseling.

Witters I, Moerman P, Natens R, Van Assche FA, Fryns JP. Witters I, et al. Genet Couns. 2002;13(2):147-9. Genet Couns. 2002. PMID: 12150214

9

Rapid prenatal diagnosis of trisomy 21 in 5049 consecutive uncultured amniotic fluid samples by fluorescence in situ hybridisation (FISH).

Witters I, Devriendt K, Legius E, Matthijs G, Van Schoubroeck D, Van Assche FA, Fryns JP. Witters I, et al. Prenat Diagn. 2002 Jan;22(1):29-33. doi: 10.1002/pd.225. Prenat Diagn. 2002. PMID: 11810646

10

Submicroscopic distal deletion of the long arm of chromosome 13(13q34) with corpus callosum agenesis.

Witters I, Chabchoub E, Vermeesch JR, Fryns JP. Witters I, et al. Am J Med Genet A. 2009 Aug;149A(8):1834-6. doi: 10.1002/ajmg.a.32978. Am J Med Genet A. 2009. PMID: 19610112 No abstract available.

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