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Biomedical Sciences Instrumentation
|
January 1, 1993
An interactive image processing system for the quantification of cardiac function in the embryonic chick
B 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-Xp22.1
H Bruyere, S Lewis, S Wood, et al.
Prenatal Diagnosis
|
November 1, 1996
De novo interstitial proximal deletion of 14q and prenatal diagnosis of holoprosencephaly
H 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 pathogenicity
C 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 report
S 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 leukemia
M J Greenwood, M D Seftel, C Richardson, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 8) with videos related to
Sort By:
Page
of 1
Biomedical Sciences Instrumentation
|
January 1, 1993
An interactive image processing system for the quantification of cardiac function in the embryonic chick
B 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-Xp22.1
H Bruyere, S Lewis, S Wood, et al.
Prenatal Diagnosis
|
November 1, 1996
De novo interstitial proximal deletion of 14q and prenatal diagnosis of holoprosencephaly
H 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 pathogenicity
C 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 report
S 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 leukemia
M J Greenwood, M D Seftel, C Richardson, et al.
Page
of 1