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Prenatal Diagnosis
|
February 1, 1990
Survival of fetuses with abnormal karyotypes and cystic hygromas detected prenatally
B N Chodirker, C R Harman, C R Greenberg
Prenatal Diagnosis
|
February 1, 1988
The BOR syndrome and renal agenesis--prenatal diagnosis and further clinical delineation
C R Greenberg, C L Trevenen, J A Evans
American Journal of Medical Genetics
|
April 1, 1991
Three years' experience with neonatal screening for Duchenne/Becker muscular dystrophy: gene analysis, gene expression, and phenotype prediction
C R Greenberg, H K Jacobs, W Halliday, et al.
American Journal of Human Genetics
|
August 1, 1987
DNA studies in a family with Duchenne muscular dystrophy and a deletion at Xp21
C R Greenberg, J L Hamerton, M Nigli, et al.
Journal of the Neurological Sciences
|
October 1, 1992
Analysis of the CAG repeat region of the androgen receptor gene in a kindred with X-linked spinal and bulbar muscular atrophy
D D Belsham, W C Yee, C R Greenberg, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
February 1, 1993
Single-blind study of dystrophin staining in carriers of Duchenne muscular dystrophy
F P Bernier, C R Greenberg, W C Halliday, et al.
Molecular Genetics and Metabolism Reports
|
March 4, 2016
A rare case of Niemann-Pick disease type C without neurological involvement in a 66-year-old patient
C R Greenberg, J G Barnes, S Kogan, et al.
Human Molecular Genetics
|
November 1, 1995
Germline mosaicism in a female who seemed to be a carrier by sequence analysis
S S Sommer, A Knöll, C R Greenberg, et al.
Human Molecular Genetics
|
April 1, 1994
TaqI polymorphism in intron 2 of the GCDH gene
J C Haworth, R Singal, S I Goodman, et al.
Genetics and Molecular Research : GMR
|
September 11, 2010
A novel COMP mutation in an Inuit patient with pseudoachondroplasia and severe short stature
A M Elliott, P Bocangel, M H Reed, et al.
Page
of 11
Search research articles
Search
Showing results (11-20 of 105) with videos related to
Sort By:
Page
of 11
Prenatal Diagnosis
|
February 1, 1990
Survival of fetuses with abnormal karyotypes and cystic hygromas detected prenatally
B N Chodirker, C R Harman, C R Greenberg
Prenatal Diagnosis
|
February 1, 1988
The BOR syndrome and renal agenesis--prenatal diagnosis and further clinical delineation
C R Greenberg, C L Trevenen, J A Evans
American Journal of Medical Genetics
|
April 1, 1991
Three years' experience with neonatal screening for Duchenne/Becker muscular dystrophy: gene analysis, gene expression, and phenotype prediction
C R Greenberg, H K Jacobs, W Halliday, et al.
American Journal of Human Genetics
|
August 1, 1987
DNA studies in a family with Duchenne muscular dystrophy and a deletion at Xp21
C R Greenberg, J L Hamerton, M Nigli, et al.
Journal of the Neurological Sciences
|
October 1, 1992
Analysis of the CAG repeat region of the androgen receptor gene in a kindred with X-linked spinal and bulbar muscular atrophy
D D Belsham, W C Yee, C R Greenberg, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
February 1, 1993
Single-blind study of dystrophin staining in carriers of Duchenne muscular dystrophy
F P Bernier, C R Greenberg, W C Halliday, et al.
Molecular Genetics and Metabolism Reports
|
March 4, 2016
A rare case of Niemann-Pick disease type C without neurological involvement in a 66-year-old patient
C R Greenberg, J G Barnes, S Kogan, et al.
Human Molecular Genetics
|
November 1, 1995
Germline mosaicism in a female who seemed to be a carrier by sequence analysis
S S Sommer, A Knöll, C R Greenberg, et al.
Human Molecular Genetics
|
April 1, 1994
TaqI polymorphism in intron 2 of the GCDH gene
J C Haworth, R Singal, S I Goodman, et al.
Genetics and Molecular Research : GMR
|
September 11, 2010
A novel COMP mutation in an Inuit patient with pseudoachondroplasia and severe short stature
A M Elliott, P Bocangel, M H Reed, et al.
Page
of 11