Standaert L - Search Results

1

Longitudinal phenotypic analysis in patients with connexin 26 (GJB2) (DFNB1) and connexin 30 (GJB6) mutations.

Stinckens C, Kremer H, van Wijk E, Hoefsloot LH, Huygen PL, Standaert L, Fryns JP, Cremers CW. Stinckens C, et al. Among authors: standaert l. Ann Otol Rhinol Laryngol. 2004 Jul;113(7):587-93. doi: 10.1177/000348940411300714. Ann Otol Rhinol Laryngol. 2004. PMID: 15274422

2

The presence of a widened vestibular aqueduct and progressive sensorineural hearing loss in the branchio-oto-renal syndrome. A family study.

Stinckens C, Standaert L, Casselman JW, Huygen PL, Kumar S, Van de Wallen J, Cremers CW. Stinckens C, et al. Among authors: standaert l. Int J Pediatr Otorhinolaryngol. 2001 Jul 2;59(3):163-72. doi: 10.1016/s0165-5876(01)00473-6. Int J Pediatr Otorhinolaryngol. 2001. PMID: 11397497

3

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: standaert l. 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.

4

De novo Robertsonian D/D type translocations: the Leuven experience.

Kleczkowska A, Fryns JP, Standaert L, van den Berghe H. Kleczkowska A, et al. Among authors: standaert l. Clin Genet. 1989 Jul;36(1):65-8. doi: 10.1111/j.1399-0004.1989.tb03368.x. Clin Genet. 1989. PMID: 2766564

5

Cohen syndrome: the clinical symptoms and stigmata at a young age.

Fryns JP, Legius E, Devriendt K, Meire F, Standaert L, Baten E, Van den Berghe H. Fryns JP, et al. Among authors: standaert l. Clin Genet. 1996 May;49(5):237-41. doi: 10.1111/j.1399-0004.1996.tb03780.x. Clin Genet. 1996. PMID: 8832131

6

Otological manifestations of CHARGE association.

Dhooge I, Lemmerling M, Lagache M, Standaert L, Govaert P, Mortier G. Dhooge I, et al. Among authors: standaert l. Ann Otol Rhinol Laryngol. 1998 Nov;107(11 Pt 1):935-41. doi: 10.1177/000348949810701106. Ann Otol Rhinol Laryngol. 1998. PMID: 9823842

7

De novo paracentric inversion in a microcephalic boy: 46,XY, inv(14)(q13q24).

Jaeken J, Fryns JP, Standaert L, De Cock P, Van den Berghe H. Jaeken J, et al. Among authors: standaert l. Ann Genet. 1980;23(2):105-7. Ann Genet. 1980. PMID: 6967281

8

Waardenburg syndrome, Hirschsprung megacolon, and Marcus Gunn ptosis.

Meire F, Standaert L, De Laey JJ, Zeng LH. Meire F, et al. Among authors: standaert l. Am J Med Genet. 1987 Jul;27(3):683-6. doi: 10.1002/ajmg.1320270322. Am J Med Genet. 1987. PMID: 3631139

9

Waardenburg syndrome.

De Laey JJ, Meire F, Standaert L, Zeng LH. De Laey JJ, et al. Among authors: standaert l. Bull Soc Belge Ophtalmol. 1985;216 Pt 2:59-68. Bull Soc Belge Ophtalmol. 1985. PMID: 3939645 No abstract available.

10

Waardenburg syndrome.

De Laey JJ, Meire F, Standaert L, Zeng LH. De Laey JJ, et al. Among authors: standaert l. Yan Ke Xue Bao. 1987 Mar;3(1):10-5. Yan Ke Xue Bao. 1987. PMID: 3149590 Chinese, English. No abstract available.

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