Recognition of pacemaker lead infection by transoesophageal echocardiography

von Van Camp, G, Vandenbossche, J L
Veröffentlicht 1991

Non-smoke spontaneous contrast in left atrium intensified by respiratory manoeuvres: a new transoesophageal echocardiographic observation.

von Van Camp, G, Cosyns, B, Vandenbossche, J L
Veröffentlicht 1994

Role of DFNA5 in hearing loss and cancer – a comment on Rakusic et al

von Croes L, Op de Beeck K, Van Camp G
Veröffentlicht 2015-09-01

Nonsyndromic hearing impairment: unparalleled heterogeneity.

von Van Camp, G, Willems, P J, Smith, R J
Veröffentlicht 1997

A polymorphic locus [D21S144] is detected by probe pVC12 on chromosome 21.

von Van Camp, G, Stinissen, P, Vandenberghe, A, Van Broeckhoven, C
Veröffentlicht 1989

Aortic valve aneurysm after acute endocarditis

von Plein, D., Van Camp, G., Derluyn, M., Vandenbossche, J.‐L.
Veröffentlicht in Clin Cardiol (2009)

Discrimination among thermophilic Campylobacter species by polymerase chain reaction amplification of 23S rRNA gene fragments.

von Eyers, M, Chapelle, S, Van Camp, G, Goossens, H, De Wachter, R
Veröffentlicht 1994

Discrimination among thermophilic Campylobacter species by polymerase chain reaction amplification of 23S rRNA gene fragments.

von Eyers, M, Chapelle, S, Van Camp, G, Goossens, H, De Wachter, R
Veröffentlicht 1993

Ruptured aortic dissection into the left atrium which presented as congestive heart failure and was diagnosed by transoesophageal echocardiography.

von Van Camp, G, Liebens, I, Silance, P G, Cham, B, Vandenbossche, J L
Veröffentlicht 1994

Genotype-phenotype correlation in L1 associated diseases.

von Fransen, E, Van Camp, G, D'Hooge, R, Vits, L, Willems, P J
Veröffentlicht 1998

An unique case of “Atypical Ebstein’s Anomaly” with only isolated displacement of the inferior tricuspid leaflet

von Tanaka, K., Van Malderen, S., Verdries, D. E., De Mey, J., Van Camp, G.
Veröffentlicht 2013

Cardiac and autonomic evaluation in a pediatric population with human immunodeficiency virus

von Plein, D., Van Camp, G., Cosyns, B., Alimenti, A., Levy, J., Vandenbossche, J.‐L.
Veröffentlicht in Clin Cardiol (2009)

Mutation of COL11A2 causes autosomal recessive non-syndromic hearing loss at the DFNB53 locus

von Chen, W, Kahrizi, K, Meyer, N, Riazalhosseini, Y, Van Camp, G, Najmabadi, H, Smith, R
Veröffentlicht 2005

A novel locus for autosomal dominant nonsyndromic hearing loss, DFNA13, maps to chromosome 6p.

von Brown, M R, Tomek, M S, Van Laer, L, Smith, S, Kenyon, J B, Van Camp, G, Smith, R J
Veröffentlicht 1997

Superior vena cava syndrome associated with Nocardia farcinica infection

von Abdelkafi, S., Dubail, D., Bosschaerts, T., Brunet, A., Van Camp, G., de Marneffe, M., De Vaster, J. M., Ninane, V.
Veröffentlicht 1997

A novel locus for autosomal dominant non-syndromic hearing loss, DFNA31, maps to chromosome 6p21.3

von Snoeckx, R, Kremer, H, Ensink, R, Flothmann, K, de Brouwer, A, Smith, R, Cremers, C, Van Camp, G
Veröffentlicht 2004

DFNA5: hearing impairment exon instead of hearing impairment gene?

von Van Laer, L, Vrijens, K, Thys, S, Van Tendeloo, V F I, Smith, R, Van Bockstaele, D R, Timmermans, J, Van Camp, G
Veröffentlicht 2004

Primary tumor sidedness has an impact on prognosis and treatment outcome in metastatic colorectal cancer: results from two randomized first-line panitumumab studies

von Boeckx, N., Koukakis, R., Op de Beeck, K., Rolfo, C., Van Camp, G., Siena, S., Tabernero, J., Douillard, J.-Y., André, T., Peeters, M.
Veröffentlicht in Ann Oncol (2017)

Chromosome 13q deletion with Waardenburg syndrome: further evidence for a gene involved in neural crest function on 13q.

von Van Camp, G, Van Thienen, M N, Handig, I, Van Roy, B, Rao, V S, Milunsky, A, Read, A P, Baldwin, C T, Farrer, L A, Bonduelle, M
Veröffentlicht 1995

Van Buchem disease (hyperostosis corticalis generalisata) maps to chromosome 17q12-q21.

von Van Hul, W, Balemans, W, Van Hul, E, Dikkers, F G, Obee, H, Stokroos, R J, Hildering, P, Vanhoenacker, F, Van Camp, G, Willems, P J
Veröffentlicht 1998