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G van Camp

Showing results (71-80 of 214) with videos related to

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European Journal of Human Genetics : EJHG|January 1, 1995
CRASH syndrome: clinical spectrum of corpus callosum hypoplasia, retardation, adducted thumbs, spastic paraparesis and hydrocephalus due to mutations in one single gene, L1E Fransen, V Lemmon, G Van Camp, et al.
Nederlands Tijdschrift Voor Geneeskunde|November 25, 2003
[From gene to disease; non-syndromic, autosomal dominant, low-frequency sensorineural hearing loss (DFNA6/14)]R J Pennings, K Cryns, P L Huygen, et al.
The American Journal of Cardiology|November 25, 2000
Comparison of transthoracic echocardiography with second harmonic imaging with transesophageal echocardiography in the detection of right to left shuntsG Van Camp, P Franken, P Melis, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation|August 1, 2013
An unique case of "Atypical Ebstein's Anomaly" with only isolated displacement of the inferior tricuspid leafletK Tanaka, S Van Malderen, D E Verdries, et al.
Clinical Cardiology|February 4, 1999
Cardiac and autonomic evaluation in a pediatric population with human immunodeficiency virusD Plein, G Van Camp, B Cosyns, et al.
Advances in Oto-Rhino-Laryngology|November 1, 2002
Pendred syndrome redefined. Report of a new family with fluctuating and progressive hearing lossC Stinckens, P L M Huygen, G Van Camp, et al.
Analytica Chimica Acta|April 30, 2013
Use of potentiometric detection in (ultra) high performance liquid chromatography and modelling with adsorption/desorption binding kineticsD Daems, G Van Camp, M Fernandez, et al.
Human Mutation|February 6, 1998
Evidence for somatic and germline mosaicism in CRASH syndromeL Vits, D Chitayat, G Van Camp, et al.
Human Genetics|April 6, 1999
Non-syndromic hearing loss associated with enlarged vestibular aqueduct is caused by PDS mutationsS Usami, S Abe, M D Weston, et al.
Human Molecular Genetics|December 1, 1994
X-linked hydrocephalus and MASA syndrome present in one family are due to a single missense mutation in exon 28 of the L1CAM geneE Fransen, C Schrander-Stumpel, L Vits, et al.
Pageof 22

Showing results (71-80 of 214) with videos related to

Sort By:
Pageof 22
European Journal of Human Genetics : EJHG|January 1, 1995
CRASH syndrome: clinical spectrum of corpus callosum hypoplasia, retardation, adducted thumbs, spastic paraparesis and hydrocephalus due to mutations in one single gene, L1E Fransen, V Lemmon, G Van Camp, et al.
Nederlands Tijdschrift Voor Geneeskunde|November 25, 2003
[From gene to disease; non-syndromic, autosomal dominant, low-frequency sensorineural hearing loss (DFNA6/14)]R J Pennings, K Cryns, P L Huygen, et al.
The American Journal of Cardiology|November 25, 2000
Comparison of transthoracic echocardiography with second harmonic imaging with transesophageal echocardiography in the detection of right to left shuntsG Van Camp, P Franken, P Melis, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation|August 1, 2013
An unique case of "Atypical Ebstein's Anomaly" with only isolated displacement of the inferior tricuspid leafletK Tanaka, S Van Malderen, D E Verdries, et al.
Clinical Cardiology|February 4, 1999
Cardiac and autonomic evaluation in a pediatric population with human immunodeficiency virusD Plein, G Van Camp, B Cosyns, et al.
Advances in Oto-Rhino-Laryngology|November 1, 2002
Pendred syndrome redefined. Report of a new family with fluctuating and progressive hearing lossC Stinckens, P L M Huygen, G Van Camp, et al.
Analytica Chimica Acta|April 30, 2013
Use of potentiometric detection in (ultra) high performance liquid chromatography and modelling with adsorption/desorption binding kineticsD Daems, G Van Camp, M Fernandez, et al.
Human Mutation|February 6, 1998
Evidence for somatic and germline mosaicism in CRASH syndromeL Vits, D Chitayat, G Van Camp, et al.
Human Genetics|April 6, 1999
Non-syndromic hearing loss associated with enlarged vestibular aqueduct is caused by PDS mutationsS Usami, S Abe, M D Weston, et al.
Human Molecular Genetics|December 1, 1994
X-linked hydrocephalus and MASA syndrome present in one family are due to a single missense mutation in exon 28 of the L1CAM geneE Fransen, C Schrander-Stumpel, L Vits, et al.
Pageof 22