Chromosome pairing in polyploid cells.
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Amnion↗
Biomedical subjects
S Kelly
Publications and source records attributed to S Kelly.
Detection of phenylketonuria carriers.
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Female↗
A fluorescent spot test for creatine kinase.
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Buffers↗
Another biochemical variant of galactosemia.
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Erythrocytes↗
A hypothesis on the homocystinuric's response to pyridoxine.
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Adolescent↗
Amino acid patterns in cystinuric families.
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Adolescent↗
The relationship between cytogenetic constitution, physical stigmata, and intelligence in Down's syndrome.
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Abnormalities, Multiple↗
Screening for hemolytic anemia in Project Headstart.
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Anemia, Sickle Cell↗
Galactose-1-phosphate uridyl transferase in mongols.
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Adolescent↗
LDH isozyme pattern in induced muscle disease (Coxsackie Group A virus infection).
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Animals↗
Amino acid abnormalities in a mentally retarded population.
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Amino Acid Metabolism, Inborn Errors↗
Effects of diagnostic x-rays on chromosomes in infants: a preliminary report.
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Angiography↗
Phenylketonuria in New York State.
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Female↗
Serum creatine phosphokinase in 4 generations of a muscular dystrophy family.
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Creatine Kinase↗
Glucose-6-phosphate dehydrogenase deficiency in Project Head Start children.
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Black or African American↗
Autosomal monosomy in a spontaneous abortion.
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Abortion, Habitual↗
METABOLISM OF MYO-INOSITOL IN PLANTS: CONVERSION TO PECTIN, HEMICELLULOSE, D-XYLOSE, AND SUGAR ACIDS.
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Journal Article↗