citrulline and Genetic Diseases

citrulline has been researched along with Genetic Diseases in 3 studies

Research

Studies (3)

Timeframe	Studies, this research(%)	All Research%
pre-1990	3 (100.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Nojima, H	1
Kohn, G; Mellman, WJ	1
Harris, H	1

Reviews

2 review(s) available for citrulline and Genetic Diseases

Article	Year
[Genetic engineering for diagnosis]. Rinsho byori. The Japanese journal of clinical pathology, 1985, Volume: 33 Spec No 65 Topics: Bacteriophages; Citrulline; Cloning, Molecular; DNA; DNA-Directed DNA Polymerase; Genetic Diseases, Inborn; Genetic Engineering; Genotype; Humans; Huntington Disease; Leukocytes; Nucleic Acid Hybridization; Oligonucleotides; Polymorphism, Genetic; RNA	1985
Molecular basis of hereditary disease. British medical journal, 1968, Apr-20, Volume: 2, Issue:5598 Topics: Acid Phosphatase; Amino Acids; Citrulline; DNA; Erythrocytes; Genetic Diseases, Inborn; Glucosephosphate Dehydrogenase; Hemoglobins; Humans; Infant, Newborn; Metabolism, Inborn Errors	1968

Other Studies

1 other study(ies) available for citrulline and Genetic Diseases

Article	Year
Human cell cultures. Their use in the investigation and diagnosis of disease. The Medical clinics of North America, 1970, Volume: 54, Issue:3 Topics: Amino Acid Metabolism, Inborn Errors; Amniotic Fluid; Carbohydrate Metabolism, Inborn Errors; Cell Line; Child; Child, Preschool; Chromosomes, Human, 21-22 and Y; Citrulline; Culture Techniques; Down Syndrome; Female; Fibroblasts; Genetic Diseases, Inborn; Glycogen Storage Disease; Glycosaminoglycans; Humans; Infant; Infant, Newborn; Lymphocytes; Malonates; Metabolism, Inborn Errors; Methane; Skin; Staining and Labeling; Trisomy	1970

Article

Year

Human cell cultures. Their use in the investigation and diagnosis of disease.

The Medical clinics of North America, 1970, Volume: 54, Issue:3

Topics: Amino Acid Metabolism, Inborn Errors; Amniotic Fluid; Carbohydrate Metabolism, Inborn Errors; Cell Line; Child; Child, Preschool; Chromosomes, Human, 21-22 and Y; Citrulline; Culture Techniques; Down Syndrome; Female; Fibroblasts; Genetic Diseases, Inborn; Glycogen Storage Disease; Glycosaminoglycans; Humans; Infant; Infant, Newborn; Lymphocytes; Malonates; Metabolism, Inborn Errors; Methane; Skin; Staining and Labeling; Trisomy

1970