Van Hole C[au] - Search Results

Year	Number of Results
1993	2
1996	1
1997	1
1998	1
2000	1
2001	1
2002	1
2004	1
2009	1
2012	1
2023	0

1

Anogenital malformation with ambiguous genitalia as part of the OEIS complex.

Witters I, Deprest J, Van Hole C, Hanssens M, Devlieger H, Fryns JP. Witters I, et al. Among authors: van hole c. Ultrasound Obstet Gynecol. 2004 Dec;24(7):797-8. doi: 10.1002/uog.1776. Ultrasound Obstet Gynecol. 2004. PMID: 15543545 Free article. Review. No abstract available.

2

Premature foetal closure of the arterial duct: clinical presentations and outcome.

Gewillig M, Brown SC, De Catte L, Debeer A, Eyskens B, Cossey V, Van Schoubroeck D, Van Hole C, Devlieger R. Gewillig M, et al. Among authors: van hole c. Eur Heart J. 2009 Jun;30(12):1530-6. doi: 10.1093/eurheartj/ehp128. Epub 2009 Apr 23. Eur Heart J. 2009. PMID: 19389789

3

Resolution of non-immune hydrops in Noonan syndrome with favorable outcome.

Witters I, Spitz B, Van Hole C, Devriendt K, Fryns JP, Verbek K. Witters I, et al. Among authors: van hole c. Am J Med Genet. 2002 Jul 15;110(4):408-9. doi: 10.1002/ajmg.10475. Am J Med Genet. 2002. PMID: 12116221 No abstract available.

4

Congenital pulmonary lymphangiectasis with chylothorax: a heterogeneous lymphatic vessel abnormality.

Moerman P, Vandenberghe K, Devlieger H, Van Hole C, Fryns JP, Lauweryns JM. Moerman P, et al. Among authors: van hole c. Am J Med Genet. 1993 Aug 1;47(1):54-8. doi: 10.1002/ajmg.1320470112. Am J Med Genet. 1993. PMID: 8368253

5

Variability in expression of a familial 2.79 Mb microdeletion in chromosome 14q22.1-22.2.

Lumaka A, Van Hole C, Casteels I, Ortibus E, De Wolf V, Vermeesch JR, Lukusa T, Devriendt K. Lumaka A, et al. Among authors: van hole c. Am J Med Genet A. 2012 Jun;158A(6):1381-7. doi: 10.1002/ajmg.a.35353. Epub 2012 May 11. Am J Med Genet A. 2012. PMID: 22581619

6

Diaphragmatic hernia as the first echographic sign in Apert syndrome.

Witters I, Devriendt K, Moerman P, van Hole C, Fryns JP. Witters I, et al. Among authors: van hole c. Prenat Diagn. 2000 May;20(5):404-6. Prenat Diagn. 2000. PMID: 10820409

7

Selective bronchial intubation for the treatment of bronchopleural fistula in a preterm newborn.

De Boeck K, Devlieger H, VanHole C, Martens M, De Zegher F. De Boeck K, et al. Chest. 1993 May;103(5):1639. doi: 10.1378/chest.103.5.1639b. Chest. 1993. PMID: 8486074 No abstract available.

8

Clinical and molecular genetic features of congenital spinal muscular atrophy.

Devriendt K, Lammens M, Schollen E, Van Hole C, Dom R, Devlieger H, Cassiman JJ, Fryns JP, Matthijs G. Devriendt K, et al. Among authors: van hole c. Ann Neurol. 1996 Nov;40(5):731-8. doi: 10.1002/ana.410400509. Ann Neurol. 1996. PMID: 8957014

9

Proteinuria in a patient with the diaphragmatic hernia-hypertelorism-myopia-deafness syndrome: further evidence that the facio-oculo-acoustico-renal syndrome represents the same entity.

Devriendt K, Standaert L, Van Hole C, Devlieger H, Fryns JP. Devriendt K, et al. Among authors: van hole c. J Med Genet. 1998 Jan;35(1):70-1. doi: 10.1136/jmg.35.1.70. J Med Genet. 1998. PMID: 9475100 Free PMC article.

10

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. Among authors: van hole c. Am J Med Genet. 2001 Dec 1;104(3):209-13. Am J Med Genet. 2001. PMID: 11754046

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

Search Page

Search Results