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Your search keyword '"Shih LY"' showing total 12 results
Start Over Author "Shih LY" Publication Year Range More than 50 years ago
12 results on '"Shih LY"'

1. Trisomy 18 mosaicism in two siblings.

Author

Shih LY, Hsu LY, Sujansky E, and Kushnick T

Subjects
Cell Line, Child, Preschool, Dermatoglyphics, Epilepsy, Tonic-Clonic genetics, Female, Fibroblasts cytology, Humans, Hydrocephalus genetics, Infant, Infant, Newborn, Karyotyping, Leukocytes cytology, Male, Microcephaly genetics, Skull abnormalities, Syndrome, Abnormalities, Multiple genetics, Chromosomes, Human, 16-18, Mosaicism, Trisomy
Published
1974
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2. Relation of mandible growth to palate closure in mice.

Author

Shih LY, Trasler DG, and Fraser FC

Subjects
Amines toxicity, Animals, Body Weight, Cleft Palate chemically induced, Cleft Palate embryology, Cortisone toxicity, Female, Gestational Age, Mandible drug effects, Mice, Niacinamide toxicity, Palate drug effects, Pregnancy, Vitamin A toxicity, Mandible embryology, Maxillofacial Development drug effects, Mice, Inbred A embryology, Mice, Inbred C57BL embryology, Palate embryology
Published
1974
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3. The distribution of genetic polymorphisms among Chinese in Taiwan.

Author

Shih LY and Hsia DY

Subjects
Acid Phosphatase blood, Adenine Nucleotides, Alkaline Phosphatase blood, Asian People, Black People, Glucosephosphate Dehydrogenase blood, Haptoglobins, Humans, Phosphoglucomutase blood, Phosphogluconate Dehydrogenase blood, Phosphotransferases blood, Taiwan, Transferrin, White People, Gene Frequency, Polymorphism, Genetic
Published
1969
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10. The distribution of genetic polymorphisms among patients with Down's syndrome, phenylketonuria, and cystic fibrosis of the pancreas.

Author

Hsia DY, Shih LY, Easterberg S, Farquhar J, Kim CB, Yeh S, and Young A

Subjects
Acid Phosphatase blood, Adenine Nucleotides blood, Child, Erythrocytes enzymology, Genes, Haptoglobins, Humans, Phenotype, Phosphoglucomutase blood, Phosphogluconate Dehydrogenase blood, Phosphotransferases blood, Transferrin analysis, Cystic Fibrosis genetics, Down Syndrome genetics, Phenylketonurias genetics, Polymorphism, Genetic
Published
1969

11. Characterization of leukocyte glucose-6-phosphate dehydrogenase in normal and mutant human subjects.

Author

Justice P, Shih LY, Gordon J, Grossman A, and Hsia DY

Subjects
Black or African American, Anemia, Hemolytic, Congenital Nonspherocytic, Cellulose, Child, Preschool, Chromatography, Thin Layer, Down Syndrome, Humans, Thalassemia, White People, Erythrocytes enzymology, Glucosephosphate Dehydrogenase analysis, Glucosephosphate Dehydrogenase Deficiency, Leukocytes enzymology
Published
1966

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