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Progress in Clinical and Biological Research
|
January 1, 1982
Genetic services in Canada: the view from Medicare
C L Clow
The New England Journal of Medicine
|
December 4, 1980
Phenylketonuria: epitome of human biochemical genetics (first of two parts)
C R Scriver, C L Clow
Pediatrics
|
January 1, 1977
Knowledge about and attitudes toward genetic screening among high-school students: the Tay-Sachs experience
C L Clow, C R Scriver
Lancet (London, England)
|
April 7, 1990
Carrier screening for Tay-Sachs disease
C R Scriver, C L Clow
The Journal of Pediatrics
|
September 1, 1988
Avoiding phenylketonuria: why parents seek prenatal diagnosis
C R Scriver, C L Clow
The New England Journal of Medicine
|
December 11, 1980
Phenylketonuria: epitome of human biochemical genetics (second of two parts)
C R Scriver, C L Clow
Lancet (London, England)
|
July 21, 1990
Carrier screening for Tay-Sachs disease
C R Scriver, C L Clow
Annual Review of Genetics
|
January 1, 1980
Phenylketonuria and other phenylalanine hydroxylation mutants in man
C R Scriver, C L Clow
Progress in Clinical and Biological Research
|
January 1, 1977
Compliance factors in Tay-Sachs screening
C R Scriver, C L Clow
Progress in Clinical and Biological Research
|
January 1, 1977
The adolescent copes with genetic screening: a study of Tay-Sachs screening among high-school students
C L Clow, C R Scriver
Page
of 5
Search research articles
Search
Showing results (1-10 of 41) with videos related to
Sort By:
Page
of 5
Progress in Clinical and Biological Research
|
January 1, 1982
Genetic services in Canada: the view from Medicare
C L Clow
The New England Journal of Medicine
|
December 4, 1980
Phenylketonuria: epitome of human biochemical genetics (first of two parts)
C R Scriver, C L Clow
Pediatrics
|
January 1, 1977
Knowledge about and attitudes toward genetic screening among high-school students: the Tay-Sachs experience
C L Clow, C R Scriver
Lancet (London, England)
|
April 7, 1990
Carrier screening for Tay-Sachs disease
C R Scriver, C L Clow
The Journal of Pediatrics
|
September 1, 1988
Avoiding phenylketonuria: why parents seek prenatal diagnosis
C R Scriver, C L Clow
The New England Journal of Medicine
|
December 11, 1980
Phenylketonuria: epitome of human biochemical genetics (second of two parts)
C R Scriver, C L Clow
Lancet (London, England)
|
July 21, 1990
Carrier screening for Tay-Sachs disease
C R Scriver, C L Clow
Annual Review of Genetics
|
January 1, 1980
Phenylketonuria and other phenylalanine hydroxylation mutants in man
C R Scriver, C L Clow
Progress in Clinical and Biological Research
|
January 1, 1977
Compliance factors in Tay-Sachs screening
C R Scriver, C L Clow
Progress in Clinical and Biological Research
|
January 1, 1977
The adolescent copes with genetic screening: a study of Tay-Sachs screening among high-school students
C L Clow, C R Scriver
Page
of 5