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Gene
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February 5, 1999
The BCL7 gene family: deletion of BCL7B in Williams syndrome
D M Jadayel, L R Osborne, L J Coignet, et al.
Human Molecular Genetics
|
August 1, 1994
Physical mapping of the split hand/split foot locus on chromosome 7 and implication in syndromic ectrodactyly
S W Scherer, P Poorkaj, H Massa, et al.
Human Molecular Genetics
|
August 24, 2005
Novel glycogen synthase kinase 3 and ubiquitination pathways in progressive myoclonus epilepsy
Hannes Lohi, Leonarda Ianzano, Xiao-Chu Zhao, et al.
Molecular Cytogenetics
|
March 22, 2014
Adult expression of a 3q13.31 microdeletion
Chelsea Lowther, Gregory Costain, Rebecca Melvin, et al.
Journal of Medical Genetics
|
June 5, 2015
Prenatal genomic microarray and sequencing in Canadian medical practice: towards consensus
Janet A Buchanan, David Chitayat, Elena Kolomietz, et al.
Anesthesiology
|
January 1, 1995
Volumetric capnography in children. Influence of growth on the alveolar plateau slope
R S Ream, M S Schreiner, J D Neff, et al.
Respiration Physiology
|
June 1, 1992
Modelling steady state pulmonary elimination of He, SF6 and CO2: effect of morphometry
G R Neufeld, J D Schwardt, S R Gobran, et al.
Blood
|
March 15, 1997
Molecular cytogenetic delineation of deletions and translocations involving chromosome band 7q22 in myeloid leukemias
K Fischer, S Fröhling, S W Scherer, et al.
Clinical Genetics
|
June 14, 2000
Holoprosencephaly, sacral anomalies, and situs ambiguus in an infant with partial monosomy 7q/trisomy 2p and SHH and HLXB9 haploinsufficiency
M J Nowaczyk, M J Huggins, D J Tomkins, et al.
Nuclear Medicine Communications
|
May 11, 1999
Gated metabolic positron emission tomography (GAPET) of the myocardium: 18F-FDG-PET to optimize recognition of myocardial hibernation
G Hör, W T Kranert, F D Maul, et al.
Page
of 92
Search research articles
Search
Showing results (431-440 of 915) with videos related to
Sort By:
Page
of 92
Gene
|
February 5, 1999
The BCL7 gene family: deletion of BCL7B in Williams syndrome
D M Jadayel, L R Osborne, L J Coignet, et al.
Human Molecular Genetics
|
August 1, 1994
Physical mapping of the split hand/split foot locus on chromosome 7 and implication in syndromic ectrodactyly
S W Scherer, P Poorkaj, H Massa, et al.
Human Molecular Genetics
|
August 24, 2005
Novel glycogen synthase kinase 3 and ubiquitination pathways in progressive myoclonus epilepsy
Hannes Lohi, Leonarda Ianzano, Xiao-Chu Zhao, et al.
Molecular Cytogenetics
|
March 22, 2014
Adult expression of a 3q13.31 microdeletion
Chelsea Lowther, Gregory Costain, Rebecca Melvin, et al.
Journal of Medical Genetics
|
June 5, 2015
Prenatal genomic microarray and sequencing in Canadian medical practice: towards consensus
Janet A Buchanan, David Chitayat, Elena Kolomietz, et al.
Anesthesiology
|
January 1, 1995
Volumetric capnography in children. Influence of growth on the alveolar plateau slope
R S Ream, M S Schreiner, J D Neff, et al.
Respiration Physiology
|
June 1, 1992
Modelling steady state pulmonary elimination of He, SF6 and CO2: effect of morphometry
G R Neufeld, J D Schwardt, S R Gobran, et al.
Blood
|
March 15, 1997
Molecular cytogenetic delineation of deletions and translocations involving chromosome band 7q22 in myeloid leukemias
K Fischer, S Fröhling, S W Scherer, et al.
Clinical Genetics
|
June 14, 2000
Holoprosencephaly, sacral anomalies, and situs ambiguus in an infant with partial monosomy 7q/trisomy 2p and SHH and HLXB9 haploinsufficiency
M J Nowaczyk, M J Huggins, D J Tomkins, et al.
Nuclear Medicine Communications
|
May 11, 1999
Gated metabolic positron emission tomography (GAPET) of the myocardium: 18F-FDG-PET to optimize recognition of myocardial hibernation
G Hör, W T Kranert, F D Maul, et al.
Page
of 92