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H Bruyere

Showing results (1-10 of 8) with videos related to

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Biomedical Sciences Instrumentation|January 1, 1993
An interactive image processing system for the quantification of cardiac function in the embryonic chickB Xu, M Magee, H Bruyere
Clinical Genetics|May 20, 1999
Confirmation of linkage in X-linked infantile spasms (West syndrome) and refinement of the disease locus to Xp21.3-Xp22.1H Bruyere, S Lewis, S Wood, et al.
Prenatal Diagnosis|November 1, 1996
De novo interstitial proximal deletion of 14q and prenatal diagnosis of holoprosencephalyH Bruyere, B Favre, S Douvier, et al.
American Journal of Medical Genetics. Part A|October 13, 2006
V37I connexin 26 allele in patients with sensorineural hearing loss: evidence of its pathogenicityC Huculak, H Bruyere, T N Nelson, et al.
Human Reproduction (Oxford, England)|October 31, 2003
Cytogenetic and molecular study of a premature male infant with 46,XX derived from ICSI: case reportS Ma, S S Tang, B Ho Yuen, et al.
Clinical Genetics|September 28, 2011
CCMG statement on direct-to-consumer genetic testing, T N Nelson, L Armstrong, et al.
European Journal of Haematology|November 15, 2002
Fulminant tumour lysis syndrome in acute myelogenous leukaemia with inv(16)(p13;q22)M D Seftel, H Bruyere, M Copland, et al.
Leukemia & Lymphoma|August 23, 2006
Leukocyte count as a predictor of death during remission induction in acute myeloid leukemiaM J Greenwood, M D Seftel, C Richardson, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Biomedical Sciences Instrumentation|January 1, 1993
An interactive image processing system for the quantification of cardiac function in the embryonic chickB Xu, M Magee, H Bruyere
Clinical Genetics|May 20, 1999
Confirmation of linkage in X-linked infantile spasms (West syndrome) and refinement of the disease locus to Xp21.3-Xp22.1H Bruyere, S Lewis, S Wood, et al.
Prenatal Diagnosis|November 1, 1996
De novo interstitial proximal deletion of 14q and prenatal diagnosis of holoprosencephalyH Bruyere, B Favre, S Douvier, et al.
American Journal of Medical Genetics. Part A|October 13, 2006
V37I connexin 26 allele in patients with sensorineural hearing loss: evidence of its pathogenicityC Huculak, H Bruyere, T N Nelson, et al.
Human Reproduction (Oxford, England)|October 31, 2003
Cytogenetic and molecular study of a premature male infant with 46,XX derived from ICSI: case reportS Ma, S S Tang, B Ho Yuen, et al.
Clinical Genetics|September 28, 2011
CCMG statement on direct-to-consumer genetic testing, T N Nelson, L Armstrong, et al.
European Journal of Haematology|November 15, 2002
Fulminant tumour lysis syndrome in acute myelogenous leukaemia with inv(16)(p13;q22)M D Seftel, H Bruyere, M Copland, et al.
Leukemia & Lymphoma|August 23, 2006
Leukocyte count as a predictor of death during remission induction in acute myeloid leukemiaM J Greenwood, M D Seftel, C Richardson, et al.
Pageof 1