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Prenatal Diagnosis
|
March 12, 1999
Molecular exclusion of haemoglobin SD disease by prenatal diagnosis
F H Fodor, C M Eng
Human Mutation
|
January 1, 1994
Molecular basis of Fabry disease: mutations and polymorphisms in the human alpha-galactosidase A gene
C M Eng, R J Desnick
Advances in Genetics
|
October 13, 2001
Experiences in molecular-based prenatal screening for Ashkenazi Jewish genetic diseases
C M Eng, R J Desnick
Genomics
|
April 1, 1992
Invariant exon skipping in the human alpha-galactosidase A pre-mRNA: Ag+1 to t substitution in a 5'-splice site causing Fabry disease
H Sakuraba, C M Eng, R J Desnick, et al.
American Journal of Medical Genetics
|
August 22, 1997
Fabry disease: molecular carrier detection and prenatal diagnosis by analysis of closely linked polymorphisms at Xq22.1
M Caggana, G A Ashley, R J Desnick, et al.
Prenatal Diagnosis
|
April 1, 1996
Molecular prenatal diagnosis of glycogen storage disease type Ia
Y Qu, J E Abdenur, C M Eng, et al.
Genomics
|
November 1, 1992
Isolation, mapping, and characterization of two cDNA clones expressed in the cerebellum
C M Eng, B A Durtschi, H Y Zoghbi, et al.
The Journal of Experimental Biology
|
December 1, 2009
The morphology of the masticatory apparatus facilitates muscle force production at wide jaw gapes in tree-gouging common marmosets (Callithrix jacchus)
C M Eng, S R Ward, C J Vinyard, et al.
Genomics
|
February 1, 1991
Mapping of multiple subunits of the neuronal nicotinic acetylcholine receptor to chromosome 15 in man and chromosome 9 in mouse
C M Eng, C A Kozak, A L Beaudet, et al.
Molecular Genetics and Metabolism
|
June 2, 2001
Nonradioactive detection of the common Connexin 26 167delT and 35delG mutations and frequencies among Ashkenazi Jews
J Dong, D R Katz, C M Eng, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 35) with videos related to
Sort By:
Page
of 4
Prenatal Diagnosis
|
March 12, 1999
Molecular exclusion of haemoglobin SD disease by prenatal diagnosis
F H Fodor, C M Eng
Human Mutation
|
January 1, 1994
Molecular basis of Fabry disease: mutations and polymorphisms in the human alpha-galactosidase A gene
C M Eng, R J Desnick
Advances in Genetics
|
October 13, 2001
Experiences in molecular-based prenatal screening for Ashkenazi Jewish genetic diseases
C M Eng, R J Desnick
Genomics
|
April 1, 1992
Invariant exon skipping in the human alpha-galactosidase A pre-mRNA: Ag+1 to t substitution in a 5'-splice site causing Fabry disease
H Sakuraba, C M Eng, R J Desnick, et al.
American Journal of Medical Genetics
|
August 22, 1997
Fabry disease: molecular carrier detection and prenatal diagnosis by analysis of closely linked polymorphisms at Xq22.1
M Caggana, G A Ashley, R J Desnick, et al.
Prenatal Diagnosis
|
April 1, 1996
Molecular prenatal diagnosis of glycogen storage disease type Ia
Y Qu, J E Abdenur, C M Eng, et al.
Genomics
|
November 1, 1992
Isolation, mapping, and characterization of two cDNA clones expressed in the cerebellum
C M Eng, B A Durtschi, H Y Zoghbi, et al.
The Journal of Experimental Biology
|
December 1, 2009
The morphology of the masticatory apparatus facilitates muscle force production at wide jaw gapes in tree-gouging common marmosets (Callithrix jacchus)
C M Eng, S R Ward, C J Vinyard, et al.
Genomics
|
February 1, 1991
Mapping of multiple subunits of the neuronal nicotinic acetylcholine receptor to chromosome 15 in man and chromosome 9 in mouse
C M Eng, C A Kozak, A L Beaudet, et al.
Molecular Genetics and Metabolism
|
June 2, 2001
Nonradioactive detection of the common Connexin 26 167delT and 35delG mutations and frequencies among Ashkenazi Jews
J Dong, D R Katz, C M Eng, et al.
Page
of 4