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G van Camp

Showing results (81-90 of 214) with videos related to

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Clinical Genetics|September 3, 2013
Broadening the phenotype of LRP2 mutations: a new mutation in LRP2 causes a predominantly ocular phenotype suggestive of Stickler syndromeI Schrauwen, M Sommen, C Claes, et al.
Antimicrobial Agents and Chemotherapy|January 30, 2024
Characterization of the resistome and predominant genetic lineages of Gram-positive bacteria causing keratitisCamille André, Andrew G Van Camp, Lawson Ung, et al.
Human Genetics|June 1, 1997
Physical mapping of the HOXA1 gene and the hnRPA2B1 gene in a YAC contig from human chromosome 7p14-p15L Van Laer, G Van Camp, E D Green, et al.
International Journal of Pediatric Otorhinolaryngology|November 9, 2001
Fluctuant, progressive hearing loss associated with Menière like vertigo in three patients with the Pendred syndromeC Stinckens, P L Huygen, F B Joosten, et al.
European Journal of Echocardiography : the Journal of the Working Group on Echocardiography of the European Society of Cardiology|March 24, 2004
Contrast harmonic imaging improves the evaluation of left ventricular function in ventilated patients: comparison with transesophageal echocardiographyB Cosyns, P El Haddad, H Lignian, et al.
European Journal of Nuclear Medicine and Molecular Imaging|September 1, 2005
Abnormal response to inotropic stimulation in young asymptomatic type I diabetic patients demonstrated by serial gated myocardial perfusion SPECT imagingC Weytjens, B Cosyns, G Van Camp, et al.
Acta Medica Austriaca|January 1, 1985
[Interferon in the treatment of multiple myeloma]R Kuzmits, H Ludwig, A Cortelezzi, et al.
Journal of the Neurological Sciences|July 17, 1998
Familial congenital hydrocephalus and aqueduct stenosis with probably autosomal dominant inheritance and variable expressionW I Verhagen, R H Bartels, E Fransen, et al.
Genomics|May 1, 1990
The pericentromeric 21 DNA marker pGSM21 (D21S13) contains an expressed HTF islandP Stinissen, W Van Hul, G Van Camp, et al.
Journal of Medical Genetics|April 10, 2009
A large deletion in GPR98 causes type IIC Usher syndrome in male and female members of an Iranian familyN Hilgert, K Kahrizi, N Dieltjens, et al.
Pageof 22

Showing results (81-90 of 214) with videos related to

Sort By:
Pageof 22
Clinical Genetics|September 3, 2013
Broadening the phenotype of LRP2 mutations: a new mutation in LRP2 causes a predominantly ocular phenotype suggestive of Stickler syndromeI Schrauwen, M Sommen, C Claes, et al.
Antimicrobial Agents and Chemotherapy|January 30, 2024
Characterization of the resistome and predominant genetic lineages of Gram-positive bacteria causing keratitisCamille André, Andrew G Van Camp, Lawson Ung, et al.
Human Genetics|June 1, 1997
Physical mapping of the HOXA1 gene and the hnRPA2B1 gene in a YAC contig from human chromosome 7p14-p15L Van Laer, G Van Camp, E D Green, et al.
International Journal of Pediatric Otorhinolaryngology|November 9, 2001
Fluctuant, progressive hearing loss associated with Menière like vertigo in three patients with the Pendred syndromeC Stinckens, P L Huygen, F B Joosten, et al.
European Journal of Echocardiography : the Journal of the Working Group on Echocardiography of the European Society of Cardiology|March 24, 2004
Contrast harmonic imaging improves the evaluation of left ventricular function in ventilated patients: comparison with transesophageal echocardiographyB Cosyns, P El Haddad, H Lignian, et al.
European Journal of Nuclear Medicine and Molecular Imaging|September 1, 2005
Abnormal response to inotropic stimulation in young asymptomatic type I diabetic patients demonstrated by serial gated myocardial perfusion SPECT imagingC Weytjens, B Cosyns, G Van Camp, et al.
Acta Medica Austriaca|January 1, 1985
[Interferon in the treatment of multiple myeloma]R Kuzmits, H Ludwig, A Cortelezzi, et al.
Journal of the Neurological Sciences|July 17, 1998
Familial congenital hydrocephalus and aqueduct stenosis with probably autosomal dominant inheritance and variable expressionW I Verhagen, R H Bartels, E Fransen, et al.
Genomics|May 1, 1990
The pericentromeric 21 DNA marker pGSM21 (D21S13) contains an expressed HTF islandP Stinissen, W Van Hul, G Van Camp, et al.
Journal of Medical Genetics|April 10, 2009
A large deletion in GPR98 causes type IIC Usher syndrome in male and female members of an Iranian familyN Hilgert, K Kahrizi, N Dieltjens, et al.
Pageof 22